Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 170850 |
|---|---|
| ensemblid | ENSG00000171126.8 |
| hgncid | 18306 |
| symbol | KCNG3 |
| name | potassium voltage-gated channel modifier subfamily G member 3 |
| refseq_nuc | NM_133329.6 |
| refseq_prot | NP_579875.1 |
| ensembl_nuc | ENST00000306078.2 |
| ensembl_prot | ENSP00000304127.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 42442017 |
| end | 42493982 |
| strand | - |
| ver | v1.2 |
| region | chr2:42442017-42493982 |
| region5000 | chr2:42437017-42498982 |
| regionname0 | KCNG3_chr2_42442017_42493982 |
| regionname5000 | KCNG3_chr2_42437017_42498982 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 436 | 342 | 88 | 72 | 126 | 16 | 38 | 100 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1311 | 334 | 81 | 72 | 125 | 16 | 38 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| c0002 | 0/0 | 1311 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| c0003 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| c0004 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| c0005 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2399 | 99 | 37 | 20 | 23 | 7 | 10 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0002 | 0/0 | 2399 | 97 | 14 | 34 | 29 | 5 | 15 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0003 | 0/0 | 2399 | 90 | 4 | 13 | 61 | 4 | 8 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0004 | 0/0 | 2399 | 21 | 11 | 0 | 7 | 0 | 3 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0005 | 0/0 | 2399 | 6 | 6 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0006 | 0/0 | 2399 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0007 | 0/0 | 2399 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0008 | 0/0 | 2400 | 4 | 3 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0009 | 0/0 | 2399 | 2 | 0 | 2 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0010 | 0/0 | 2399 | 2 | 1 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0011 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0012 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0013 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0014 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0015 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0016 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0017 | 0/0 | 2399 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0018 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0019 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0020 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| t0021 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0309 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1311 | 334 | 81 | 72 | 125 | 16 | 38 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0002 | 0/0 | 1311 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0003 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0004 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0005 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3709 | 97 | 35 | 20 | 23 | 7 | 10 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0002 | 0/0 | 3709 | 97 | 14 | 34 | 29 | 5 | 15 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0003 | 0/0 | 3709 | 90 | 4 | 13 | 61 | 4 | 8 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0004 | 0/0 | 3709 | 20 | 11 | 0 | 6 | 0 | 3 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0005 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0006 | 0/0 | 3709 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0007 | 0/0 | 3709 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0008 | 0/0 | 3710 | 4 | 3 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0009 | 0/0 | 3709 | 2 | 0 | 2 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0010 | 0/0 | 3709 | 2 | 1 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0011 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0012 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0013 | 0/0 | 3709 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0014 | 0/0 | 3709 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0015 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0016 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0017 | 0/0 | 3709 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0018 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0019 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0020 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0001t0021 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0002t0005 | 0/0 | 3709 | 5 | 5 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0003t0001 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0004t0001 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| a0001c0005t0004 | 0/0 | 3709 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | copy fasta | chr2 | 42437017 | 42498982 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0309 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0008g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0017g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0020g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0001t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| a0001c0005t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | GBR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0031 | EUR | GBR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00544 | hp2 | a0001 | c0001 | t0019 | g0025 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00609 | hp2 | a0001 | c0001 | t0018 | g0094 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0089 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0133 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0169 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0107 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0324 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01981 | hp2 | a0001 | c0001 | t0017 | g0171 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0283 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02083 | hp2 | a0001 | c0001 | t0015 | g0033 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0325 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CDX | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CDX | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CDX | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0333 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0268 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0088 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02735 | hp2 | a0001 | c0001 | t0014 | g0078 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0179 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03453 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03834 | hp1 | a0001 | c0001 | t0013 | g0011 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CHB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19005 | hp1 | a0001 | c0005 | t0004 | g0339 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0337 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0142 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19079 | hp1 | a0001 | c0001 | t0020 | g0183 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0087 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0331 | AFR | ASW | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ASW | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | TSI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | TSI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0036 | EUR | TSI | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | GIH | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | GIH | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0338 | AFR | ACB | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | MSL | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | USA | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | USA | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | USA | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | USA | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0309 | REF | REF | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | KCNG3_chr2_42437017_42498982 | KCNG3 | chr2 | 42437017 | 42498982 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:42493175
|
C | T | 1 | a0001c0002 | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.327G>A | p.Glu109Glu | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 808/3709 | 327/1311 | 109/436 | chr2 | 42493175 | ||
| chr2:42493328
|
G | A | 1 | a0001c0003 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.174C>T | p.Arg58Arg | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 655/3709 | 174/1311 | 58/436 | chr2 | 42493328 | ||
| chr2:42493412
|
G | A | 1 | a0001c0004 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.90C>T | p.Phe30Phe | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 571/3709 | 90/1311 | 30/436 | chr2 | 42493412 | ||
| chr2:42493463
|
C | A | 1 | a0001c0005 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.39G>T | p.Leu13Leu | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 520/3709 | 39/1311 | 13/436 | chr2 | 42493463 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:42442021
|
T | C | 1 | a0001c0001t0008 | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1913A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 1913 | chr2 | 42442021 | |||||
| chr2:42442031
|
A | AT | 1 | a0001c0001t0008 | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1902dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 1902 | chr2 | 42442031 | |||||
| chr2:42442133
|
T | C | 1 | a0001c0001t0018 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 1801 | chr2 | 42442133 | |||||
| chr2:42442480
|
T | C | 5 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(2): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1454A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 1454 | chr2 | 42442480 | |||||
| chr2:42442718
|
T | C | 5 | a0001c0001t0004a0001c0001t0013a0001c0001t0019others(2): Show | 24 | HG00544.hp2 HG02602.hp1 HG02615.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1216A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 1216 | chr2 | 42442718 | |||||
| chr2:42443042
|
T | C | 1 | a0001c0001t0019 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 892 | chr2 | 42443042 | |||||
| chr2:42443054
|
G | A | 1 | a0001c0001t0020 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 880 | chr2 | 42443054 | |||||
| chr2:42443225
|
T | C | 2 | a0001c0001t0005a0001c0002t0005 | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*709A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 709 | chr2 | 42443225 | |||||
| chr2:42443229
|
G | A | 1 | a0001c0001t0017 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 705 | chr2 | 42443229 | |||||
| chr2:42443258
|
A | T | 8 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(5): Show | 110 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*676T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 676 | chr2 | 42443258 | |||||
| chr2:42443316
|
C | T | 1 | a0001c0001t0015 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 618 | chr2 | 42443316 | |||||
| chr2:42443398
|
T | C | 1 | a0001c0001t0010 | 2 | HG01243.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*536A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 536 | chr2 | 42443398 | |||||
| chr2:42443649
|
G | A | 1 | a0001c0001t0012 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*285C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 285 | chr2 | 42443649 | |||||
| chr2:42443707
|
C | T | 1 | a0001c0001t0009 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*227G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 227 | chr2 | 42443707 | |||||
| chr2:42443752
|
T | C | 1 | a0001c0001t0007 | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*182A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 182 | chr2 | 42443752 | |||||
| chr2:42443762
|
A | G | 1 | a0001c0001t0014 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 172 | chr2 | 42443762 | |||||
| chr2:42443831
|
G | A | 1 | a0001c0001t0021 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 103 | chr2 | 42443831 | |||||
| chr2:42443850
|
T | C | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(1): Show | 15 | HG01106.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 2/2 | 84 | chr2 | 42443850 | |||||
| chr2:42493520
|
C | T | 1 | a0001c0001t0013 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 19 | chr2 | 42493520 | |||||
| chr2:42493580
|
G | T | 2 | a0001c0001t0006a0001c0001t0012 | 6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-79C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 79 | chr2 | 42493580 | |||||
| chr2:42493964
|
C | G | 1 | a0001c0001t0011 | 1 | NA18951.hp2 | 5_prime_UTR_variant | MODIFIER | c.-463G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/2 | 463 | chr2 | 42493964 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:42444609
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.666-30T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444609 | ||||||
| chr2:42444711
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.666-132G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444711 | ||||||
| chr2:42444773
|
A | C | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-194T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444773 | ||||||
| chr2:42444802
|
A | G | 115 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0106others(112): Show | 115 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.666-223T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444802 | ||||||
| chr2:42444872
|
G | C | 2 | a0001c0001t0003g0252a0001c0001t0003g0258 | 2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.666-293C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444872 | ||||||
| chr2:42444898
|
CA | C | 281 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0128others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.666-320delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444898 | ||||||
| chr2:42444901
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-322T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444901 | ||||||
| chr2:42444911
|
C | T | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-332G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444911 | ||||||
| chr2:42444940
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.666-361G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444940 | ||||||
| chr2:42444961
|
G | A | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-382C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42444961 | ||||||
| chr2:42445073
|
T | TA | 94 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0106others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.666-495dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445073 | ||||||
| chr2:42445073
|
TA | T | 144 | a0001c0001t0001g0090a0001c0001t0001g0102a0001c0001t0001g0116others(141): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.666-495delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445073 | ||||||
| chr2:42445073
|
TAA | T | 9 | a0001c0001t0003g0029a0001c0001t0003g0038a0001c0001t0003g0051others(6): Show | 9 | HG01070.hp1 HG01515.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.666-496_666-495del others(2): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445073 | ||||||
| chr2:42445074
|
A | T | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0190others(3): Show | 6 | HG00423.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-495T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445074 | ||||||
| chr2:42445075
|
A | T | 6 | a0001c0001t0007g0268a0001c0001t0007g0284a0001c0001t0008g0088others(3): Show | 6 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-496T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445075 | ||||||
| chr2:42445158
|
C | G | 25 | a0001c0001t0001g0132a0001c0001t0004g0086a0001c0001t0004g0092others(22): Show | 25 | HG00544.hp2 HG02602.hp1 HG02615.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-579G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445158 | ||||||
| chr2:42445168
|
T | A | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-589A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445168 | ||||||
| chr2:42445169
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260 | 3 | HG02723.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.666-590T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445169 | ||||||
| chr2:42445174
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-595T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445174 | ||||||
| chr2:42445175
|
T | A | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-596A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445175 | ||||||
| chr2:42445353
|
G | A | 1 | a0001c0001t0003g0185 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.666-774C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445353 | ||||||
| chr2:42445388
|
C | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-809G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445388 | ||||||
| chr2:42445438
|
G | A | 102 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0106others(99): Show | 102 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.666-859C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445438 | ||||||
| chr2:42445508
|
G | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0288a0001c0001t0003g0293 | 4 | NA18954.hp2 NA18983.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-929C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445508 | ||||||
| chr2:42445591
|
A | G | 283 | a0001c0001t0001g0058a0001c0001t0001g0077a0001c0001t0001g0090others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.666-1012T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445591 | ||||||
| chr2:42445628
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-1049T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445628 | ||||||
| chr2:42445629
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-1050C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445629 | ||||||
| chr2:42445630
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.666-1051T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445630 | ||||||
| chr2:42445652
|
A | G | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-1073T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445652 | ||||||
| chr2:42445733
|
CT | C | 214 | a0001c0001t0001g0248a0001c0001t0002g0017a0001c0001t0002g0032others(211): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.666-1155delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445733 | ||||||
| chr2:42445765
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.666-1186G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445765 | ||||||
| chr2:42445829
|
C | G | 6 | a0001c0001t0005g0209a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-1250G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445829 | ||||||
| chr2:42445831
|
A | G | 1 | a0001c0001t0003g0045 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.666-1252T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445831 | ||||||
| chr2:42445835
|
T | G | 2 | a0001c0001t0003g0034a0001c0001t0003g0101 | 2 | HG01255.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.666-1256A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445835 | ||||||
| chr2:42445916
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG01109.hp2 HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.666-1337C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445916 | ||||||
| chr2:42445978
|
C | A | 20 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(17): Show | 20 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-1399G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42445978 | ||||||
| chr2:42446062
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.666-1483C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446062 | ||||||
| chr2:42446106
|
G | C | 2 | a0001c0001t0004g0179a0001c0001t0013g0011 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.666-1527C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446106 | ||||||
| chr2:42446192
|
A | G | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-1613T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446192 | ||||||
| chr2:42446681
|
T | C | 6 | a0001c0001t0005g0209a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-2102A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446681 | ||||||
| chr2:42446853
|
G | T | 97 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.666-2274C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446853 | ||||||
| chr2:42446921
|
G | C | 30 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0187others(27): Show | 30 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.666-2342C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42446921 | ||||||
| chr2:42447080
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.666-2501G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447080 | ||||||
| chr2:42447083
|
C | CAAAAAAA others(306): Show |
1 | a0001c0001t0001g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.666-2505_666-2504i others(315): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447083 | ||||||
| chr2:42447083
|
C | CAAAAAAA others(323): Show |
1 | a0001c0001t0001g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.666-2505_666-2504i others(332): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447083 | ||||||
| chr2:42447083
|
C | CAAAAAAA others(334): Show |
1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.666-2505_666-2504i others(343): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447083 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(341): Show |
1 | a0001c0001t0001g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.666-2516_666-2515i others(350): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(331): Show |
1 | a0001c0001t0001g0297 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.666-2516_666-2515i others(340): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(329): Show |
1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.666-2516_666-2515i others(338): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(327): Show |
1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.666-2516_666-2515i others(336): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(326): Show |
3 | a0001c0001t0001g0224a0001c0001t0001g0301a0001c0001t0001g0304 | 3 | HG01169.hp2 HG01517.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.666-2516_666-2515i others(335): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(325): Show |
11 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0202others(8): Show | 11 | HG00099.hp2 HG01168.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-2516_666-2515i others(334): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(324): Show |
3 | a0001c0001t0001g0205a0001c0001t0001g0245a0001c0001t0001g0285 | 3 | HG03516.hp2 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.666-2516_666-2515i others(333): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(312): Show |
1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-2516_666-2515i others(321): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(327): Show |
3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0199 | 3 | HG01884.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.666-2516_666-2515i others(336): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(326): Show |
3 | a0001c0001t0001g0189a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02723.hp2 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.666-2516_666-2515i others(335): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447094
|
A | AGGGGGCC others(325): Show |
3 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0308 | 3 | HG01099.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.666-2516_666-2515i others(334): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447094 | ||||||
| chr2:42447112
|
G | A | 20 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(17): Show | 20 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-2533C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447112 | ||||||
| chr2:42447225
|
C | A | 6 | a0001c0001t0005g0209a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-2646G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447225 | ||||||
| chr2:42447288
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-2709T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447288 | ||||||
| chr2:42447299
|
TAC | T | 22 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(19): Show | 22 | HG01099.hp1 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.666-2722_666-2721d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447299 | ||||||
| chr2:42447519
|
CT | C | 98 | a0001c0001t0001g0248a0001c0001t0002g0272a0001c0001t0003g0003others(95): Show | 99 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.666-2941delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447519 | ||||||
| chr2:42447581
|
T | C | 89 | a0001c0001t0001g0128a0001c0001t0001g0280a0001c0001t0001g0296others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.666-3002A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447581 | ||||||
| chr2:42447601
|
A | G | 281 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0128others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.666-3022T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42447601 | ||||||
| chr2:42448101
|
G | A | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-3522C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448101 | ||||||
| chr2:42448105
|
A | G | 101 | a0001c0001t0001g0128a0001c0001t0001g0280a0001c0001t0001g0296others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.666-3526T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448105 | ||||||
| chr2:42448184
|
G | C | 20 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(17): Show | 20 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-3605C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448184 | ||||||
| chr2:42448246
|
C | G | 1 | a0001c0001t0002g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.666-3667G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448246 | ||||||
| chr2:42448344
|
C | CTTAT | 73 | a0001c0001t0001g0248a0001c0001t0003g0022a0001c0001t0003g0023others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.666-3769_666-3766d others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
C | CTTATTTA others(1): Show |
13 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0031others(10): Show | 13 | HG00140.hp2 HG01255.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.666-3773_666-3766d others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
C | CTTATTTA others(5): Show |
2 | a0001c0001t0003g0049a0001c0001t0003g0258 | 2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.666-3777_666-3766d others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
C | CTTATTTA others(9): Show |
1 | a0001c0001t0003g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.666-3781_666-3766d others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
CTTAT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.666-3769_666-3766d others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
CTTATTTA others(1): Show |
C | 41 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0189others(38): Show | 41 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.666-3773_666-3766d others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
CTTATTTA others(5): Show |
C | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.666-3777_666-3766d others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448344
|
CTTATTTA others(9): Show |
C | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.666-3781_666-3766d others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448344 | ||||||
| chr2:42448377
|
T | C | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-3798A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448377 | ||||||
| chr2:42448383
|
A | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-3804T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448383 | ||||||
| chr2:42448399
|
G | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0336 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.666-3820C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448399 | ||||||
| chr2:42448520
|
A | G | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | NA18952.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.666-3941T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448520 | ||||||
| chr2:42448552
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.666-3973C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448552 | ||||||
| chr2:42448557
|
A | G | 2 | a0001c0001t0004g0092a0001c0001t0004g0242 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.666-3978T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448557 | ||||||
| chr2:42448769
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-4190G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448769 | ||||||
| chr2:42448973
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666-4394C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448973 | ||||||
| chr2:42448977
|
C | CA | 12 | a0001c0001t0001g0093a0001c0001t0002g0315a0001c0001t0003g0069others(9): Show | 12 | HG01106.hp2 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-4399dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42448977 | ||||||
| chr2:42449177
|
G | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-4598C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449177 | ||||||
| chr2:42449194
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.666-4615G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449194 | ||||||
| chr2:42449267
|
G | A | 82 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0109others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.666-4688C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449267 | ||||||
| chr2:42449471
|
G | GA | 97 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.666-4893dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449471 | ||||||
| chr2:42449514
|
CT | C | 149 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0203others(146): Show | 150 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.666-4936delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449514 | ||||||
| chr2:42449514
|
CTT | C | 77 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0109others(74): Show | 77 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.666-4937_666-4936d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449514 | ||||||
| chr2:42449643
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.666-5064C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449643 | ||||||
| chr2:42449712
|
G | A | 97 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0109others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.666-5133C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449712 | ||||||
| chr2:42449718
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.666-5139A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449718 | ||||||
| chr2:42449753
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.666-5174C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449753 | ||||||
| chr2:42449844
|
C | A | 2 | a0001c0001t0003g0031a0001c0001t0003g0227 | 2 | HG00140.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.666-5265G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42449844 | ||||||
| chr2:42450013
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-5434A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450013 | ||||||
| chr2:42450053
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.666-5474A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450053 | ||||||
| chr2:42450409
|
T | G | 97 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.666-5830A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450409 | ||||||
| chr2:42450447
|
C | T | 83 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0109others(80): Show | 83 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.666-5868G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450447 | ||||||
| chr2:42450529
|
A | G | 1 | a0001c0001t0002g0160 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.666-5950T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450529 | ||||||
| chr2:42450734
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.666-6155G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450734 | ||||||
| chr2:42450748
|
G | A | 280 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0128others(277): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.666-6169C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450748 | ||||||
| chr2:42450773
|
T | G | 1 | a0001c0001t0013g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.666-6194A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450773 | ||||||
| chr2:42450786
|
A | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260others(1): Show | 4 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-6207T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450786 | ||||||
| chr2:42450818
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.666-6239T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450818 | ||||||
| chr2:42450889
|
T | A | 92 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(89): Show | 93 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.666-6310A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450889 | ||||||
| chr2:42450904
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260others(1): Show | 4 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-6325G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450904 | ||||||
| chr2:42450906
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.666-6327A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42450906 | ||||||
| chr2:42451118
|
C | T | 281 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0128others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.666-6539G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451118 | ||||||
| chr2:42451135
|
GC | G | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-6557delG | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451135 | ||||||
| chr2:42451154
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.666-6575C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451154 | ||||||
| chr2:42451204
|
C | CA | 71 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0058others(68): Show | 72 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.666-6626dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451204 | ||||||
| chr2:42451204
|
C | CAA | 28 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0182others(25): Show | 28 | HG00423.hp1 HG00738.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-6627_666-6626d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451204 | ||||||
| chr2:42451204
|
C | CAAA | 10 | a0001c0001t0002g0220a0001c0001t0002g0235a0001c0001t0002g0300others(7): Show | 10 | HG01928.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-6628_666-6626d others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451204 | ||||||
| chr2:42451204
|
CA | C | 130 | a0001c0001t0001g0248a0001c0001t0001g0264a0001c0001t0001g0310others(127): Show | 131 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.666-6626delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451204 | ||||||
| chr2:42451204
|
CAA | C | 19 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0109others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.666-6627_666-6626d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451204 | ||||||
| chr2:42451289
|
T | G | 1 | a0001c0001t0004g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.666-6710A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451289 | ||||||
| chr2:42451340
|
G | A | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-6761C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451340 | ||||||
| chr2:42451349
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.666-6770C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451349 | ||||||
| chr2:42451394
|
A | G | 29 | a0001c0001t0001g0132a0001c0001t0004g0086a0001c0001t0004g0092others(26): Show | 29 | HG00544.hp2 HG01106.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.666-6815T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451394 | ||||||
| chr2:42451407
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.666-6828T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451407 | ||||||
| chr2:42451506
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-6927G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451506 | ||||||
| chr2:42451594
|
G | A | 1 | a0001c0001t0003g0289 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.666-7015C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451594 | ||||||
| chr2:42451645
|
GA | G | 6 | a0001c0001t0005g0209a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-7067delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42451645 | ||||||
| chr2:42452130
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0282 | 2 | HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.666-7551C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452130 | ||||||
| chr2:42452144
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.666-7565A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452144 | ||||||
| chr2:42452220
|
A | AAT | 8 | a0001c0001t0001g0095a0001c0001t0001g0202a0001c0001t0001g0211others(5): Show | 8 | HG01192.hp1 HG01934.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.666-7643_666-7642d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATAT | 7 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0090others(4): Show | 7 | HG00735.hp1 HG01192.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-7645_666-7642d others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(1): Show |
3 | a0001c0001t0001g0203a0001c0001t0002g0221a0001c0001t0018g0094 | 3 | HG00609.hp2 HG01358.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.666-7649_666-7642d others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.666-7651_666-7642d others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0023 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.666-7653_666-7642d others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(9): Show |
2 | a0001c0001t0003g0060a0001c0001t0003g0063 | 2 | NA18946.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.666-7657_666-7642d others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(15): Show |
1 | a0001c0001t0006g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.666-7663_666-7642d others(24): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452220
|
A | AATATATA others(17): Show |
1 | a0001c0001t0003g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.666-7665_666-7642d others(26): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452220 | ||||||
| chr2:42452241
|
ATATTT | A | 14 | a0001c0001t0004g0086a0001c0001t0004g0137a0001c0001t0004g0149others(11): Show | 14 | HG00544.hp2 HG02809.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.666-7667_666-7663d others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452241 | ||||||
| chr2:42452242
|
TA | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01243.hp2 HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.666-7664delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452242 | ||||||
| chr2:42452243
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0003g0069a0001c0001t0003g0231 | 2 | HG00673.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(15): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.666-7665_666-7664i others(17): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0003g0024a0001c0001t0003g0028a0001c0001t0003g0062others(1): Show | 4 | NA18966.hp2 NA18967.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(19): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.666-7665_666-7664i others(21): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(23): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0006g0010 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(27): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0003g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.666-7665_666-7664i others(31): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(21): Show |
3 | a0001c0001t0006g0006a0001c0001t0006g0008a0001c0001t0006g0009 | 3 | HG02896.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(30): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0003g0263a0001c0001t0012g0007 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(27): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0261 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.666-7665_666-7664i others(24): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(25): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0003g0039a0001c0001t0003g0070a0001c0001t0003g0251others(1): Show | 4 | HG00544.hp1 HG01071.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(22): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(14): Show |
4 | a0001c0001t0003g0052a0001c0001t0003g0055a0001c0001t0003g0065others(1): Show | 4 | HG02523.hp2 HG03688.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(23): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0003g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(26): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0003g0049a0001c0001t0003g0056a0001c0001t0003g0057others(2): Show | 5 | HG02165.hp1 HG02165.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(20): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0003g0207a0001c0001t0003g0250 | 2 | HG01255.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(21): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0003g0038a0001c0001t0003g0104a0001c0001t0003g0229others(1): Show | 4 | NA18947.hp1 NA18951.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(22): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0103a0001c0001t0003g0115 | 2 | HG02922.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(23): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(9): Show |
6 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0043others(3): Show | 6 | HG01123.hp2 HG01167.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0248a0001c0001t0003g0228a0001c0001t0003g0252 | 3 | HG02083.hp1 NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(19): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0003g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(20): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0003g0064a0001c0001t0003g0227 | 2 | HG00639.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(8): Show |
10 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0047others(7): Show | 10 | HG02027.hp2 HG02155.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(17): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(9): Show |
5 | a0001c0001t0003g0054a0001c0001t0003g0059a0001c0001t0003g0066others(2): Show | 5 | HG00621.hp1 HG00621.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0003g0029a0001c0001t0003g0290 | 2 | HG01070.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(15): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(7): Show |
11 | a0001c0001t0003g0031a0001c0001t0003g0035a0001c0001t0003g0040others(8): Show | 11 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0003g0293 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(10): Show |
5 | a0001c0001t0003g0003a0001c0001t0003g0048a0001c0001t0003g0091others(2): Show | 6 | HG02135.hp1 NA18954.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-7665_666-7664i others(19): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0101 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.666-7665_666-7664i others(15): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0003g0034a0001c0001t0003g0257 | 2 | HG01255.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.666-7665_666-7664i others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
A | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0215a0001c0001t0001g0287others(2): Show | 5 | HG02615.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-7664T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
AT | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0084a0001c0001t0001g0126others(30): Show | 33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.666-7665delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
ATT | A | 17 | a0001c0001t0001g0238a0001c0001t0002g0017a0001c0001t0002g0117others(14): Show | 17 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-7666_666-7665d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
ATTT | A | 42 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0001t0002g0135others(39): Show | 42 | HG00673.hp1 HG00733.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.666-7667_666-7665d others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452243
|
ATTTT | A | 7 | a0001c0001t0002g0140a0001c0001t0002g0152a0001c0001t0002g0173others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-7668_666-7665d others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452243 | ||||||
| chr2:42452244
|
T | TA | 17 | a0001c0001t0001g0128a0001c0001t0001g0213a0001c0001t0001g0297others(14): Show | 17 | HG00099.hp2 HG01070.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-7666_666-7665i others(3): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452244 | ||||||
| chr2:42452244
|
T | TATATATA others(8): Show |
1 | a0001c0001t0002g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.666-7666_666-7665i others(17): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452244 | ||||||
| chr2:42452244
|
T | TATATATA others(10): Show |
1 | a0001c0001t0003g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.666-7666_666-7665i others(19): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452244 | ||||||
| chr2:42452245
|
T | A | 41 | a0001c0001t0001g0030a0001c0001t0001g0074a0001c0001t0001g0077others(38): Show | 41 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.666-7666A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452245 | ||||||
| chr2:42452246
|
T | A | 24 | a0001c0001t0001g0127a0001c0001t0001g0187a0001c0001t0001g0188others(21): Show | 24 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.666-7667A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452246 | ||||||
| chr2:42452247
|
T | A | 14 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0203others(11): Show | 14 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-7668A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452247 | ||||||
| chr2:42452248
|
T | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0232 | 2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.666-7669A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452248 | ||||||
| chr2:42452249
|
T | A | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0004g0156 | 3 | HG02055.hp1 HG02738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.666-7670A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452249 | ||||||
| chr2:42452295
|
G | C | 1 | a0001c0001t0010g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.666-7716C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452295 | ||||||
| chr2:42452370
|
T | C | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7791A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452370 | ||||||
| chr2:42452415
|
T | A | 32 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(29): Show | 32 | HG01099.hp1 HG01109.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.666-7836A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452415 | ||||||
| chr2:42452488
|
T | C | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-7909A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452488 | ||||||
| chr2:42452501
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.666-7922A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452501 | ||||||
| chr2:42452523
|
G | A | 97 | a0001c0001t0001g0248a0001c0001t0002g0180a0001c0001t0003g0003others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.666-7944C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452523 | ||||||
| chr2:42452543
|
G | A | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7964C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452543 | ||||||
| chr2:42452644
|
T | G | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-8065A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452644 | ||||||
| chr2:42452770
|
G | GGT | 112 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(109): Show | 113 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.666-8193_666-8192d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452770 | ||||||
| chr2:42452770
|
G | GGTGT | 87 | a0001c0001t0001g0090a0001c0001t0001g0139a0001c0001t0001g0216others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.666-8195_666-8192d others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452770 | ||||||
| chr2:42452770
|
G | GGTGTGT | 13 | a0001c0001t0001g0128a0001c0001t0001g0301a0001c0001t0001g0302others(10): Show | 13 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.666-8197_666-8192d others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452770 | ||||||
| chr2:42452770
|
GGT | G | 57 | a0001c0001t0001g0058a0001c0001t0001g0132a0001c0001t0001g0202others(54): Show | 57 | HG00544.hp2 HG01109.hp2 HG01516.hp2 others(54): Show |
intron_variant | MODIFIER | c.666-8193_666-8192d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452770 | ||||||
| chr2:42452770
|
GGTGTGTG others(1): Show |
G | 10 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(7): Show | 10 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-8199_666-8192d others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452770 | ||||||
| chr2:42452855
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.666-8276G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452855 | ||||||
| chr2:42452868
|
G | A | 6 | a0001c0001t0002g0320a0001c0001t0007g0267a0001c0001t0007g0268others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-8289C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452868 | ||||||
| chr2:42452902
|
A | C | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.666-8323T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42452902 | ||||||
| chr2:42453057
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260 | 3 | HG02723.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.666-8478G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453057 | ||||||
| chr2:42453138
|
T | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.666-8559A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453138 | ||||||
| chr2:42453340
|
C | T | 1 | a0001c0001t0003g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.666-8761G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453340 | ||||||
| chr2:42453468
|
C | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0285others(1): Show | 4 | HG01516.hp2 HG01517.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-8889G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453468 | ||||||
| chr2:42453643
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.666-9064A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453643 | ||||||
| chr2:42453679
|
C | T | 93 | a0001c0001t0001g0248a0001c0001t0002g0180a0001c0001t0003g0003others(90): Show | 94 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.666-9100G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453679 | ||||||
| chr2:42453751
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0233 | 2 | HG00741.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.666-9172C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453751 | ||||||
| chr2:42453798
|
G | C | 1 | a0001c0001t0003g0028 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.666-9219C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42453798 | ||||||
| chr2:42454021
|
T | A | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9442A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454021 | ||||||
| chr2:42454075
|
T | C | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-9496A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454075 | ||||||
| chr2:42454093
|
CA | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.666-9515delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454093 | ||||||
| chr2:42454274
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-9695T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454274 | ||||||
| chr2:42454327
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.666-9748A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454327 | ||||||
| chr2:42454373
|
A | G | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-9794T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454373 | ||||||
| chr2:42454396
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.666-9817A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454396 | ||||||
| chr2:42454461
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.666-9882G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454461 | ||||||
| chr2:42454557
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.666-9978G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454557 | ||||||
| chr2:42454558
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.666-9979C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454558 | ||||||
| chr2:42454683
|
C | T | 10 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(7): Show | 10 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-10104G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454683 | ||||||
| chr2:42454728
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.666-10149C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454728 | ||||||
| chr2:42454759
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.666-10180C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454759 | ||||||
| chr2:42454890
|
G | T | 1 | a0001c0001t0001g0309 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.666-10311C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42454890 | ||||||
| chr2:42455022
|
T | C | 5 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0001g0247others(2): Show | 5 | HG01099.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10443A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455022 | ||||||
| chr2:42455038
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.666-10459A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455038 | ||||||
| chr2:42455061
|
A | T | 6 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-10482T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455061 | ||||||
| chr2:42455258
|
C | A | 5 | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0136others(2): Show | 5 | HG01993.hp1 HG02004.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10679G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455258 | ||||||
| chr2:42455282
|
C | T | 2 | a0001c0001t0003g0046a0001c0001t0003g0115 | 2 | NA18954.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.666-10703G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455282 | ||||||
| chr2:42455441
|
C | G | 93 | a0001c0001t0001g0248a0001c0001t0002g0180a0001c0001t0003g0003others(90): Show | 94 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.666-10862G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455441 | ||||||
| chr2:42455507
|
T | C | 2 | a0001c0001t0010g0133a0001c0001t0010g0333 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.666-10928A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455507 | ||||||
| chr2:42455635
|
G | C | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-11056C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455635 | ||||||
| chr2:42455677
|
G | A | 10 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(7): Show | 10 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-11098C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455677 | ||||||
| chr2:42455696
|
G | C | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.666-11117C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455696 | ||||||
| chr2:42455744
|
A | C | 1 | a0001c0001t0003g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.666-11165T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455744 | ||||||
| chr2:42455778
|
A | ATAAAAAT | 3 | a0001c0001t0003g0052a0001c0001t0003g0055a0001c0001t0003g0065 | 3 | HG02523.hp2 NA18990.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.666-11206_666-1120 others(11): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455778 | ||||||
| chr2:42455835
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0288a0001c0001t0003g0293 | 4 | NA18954.hp2 NA18983.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-11256C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455835 | ||||||
| chr2:42455942
|
T | C | 10 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-11363A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42455942 | ||||||
| chr2:42456127
|
C | G | 25 | a0001c0001t0001g0132a0001c0001t0002g0326a0001c0001t0004g0092others(22): Show | 25 | HG00544.hp2 HG01106.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-11548G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456127 | ||||||
| chr2:42456172
|
A | G | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-11593T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456172 | ||||||
| chr2:42456227
|
C | T | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-11648G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456227 | ||||||
| chr2:42456245
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666-11666C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456245 | ||||||
| chr2:42456312
|
T | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0075others(8): Show | 11 | HG00741.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-11733A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456312 | ||||||
| chr2:42456314
|
T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-11735A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456314 | ||||||
| chr2:42456327
|
G | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.666-11748C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456327 | ||||||
| chr2:42456471
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-11892G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456471 | ||||||
| chr2:42456709
|
C | T | 6 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0008others(3): Show | 6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-12130G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456709 | ||||||
| chr2:42456786
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0114 | 2 | HG00741.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.666-12207G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456786 | ||||||
| chr2:42456865
|
C | T | 2 | a0001c0001t0002g0159a0001c0001t0002g0163 | 2 | NA18979.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.666-12286G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456865 | ||||||
| chr2:42456913
|
T | C | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-12334A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456913 | ||||||
| chr2:42456935
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.666-12356C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42456935 | ||||||
| chr2:42457012
|
T | G | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-12433A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457012 | ||||||
| chr2:42457330
|
G | GA | 97 | a0001c0001t0001g0248a0001c0001t0002g0180a0001c0001t0002g0312others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.666-12752dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457330 | ||||||
| chr2:42457448
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.666-12869A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457448 | ||||||
| chr2:42457472
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.666-12893G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457472 | ||||||
| chr2:42457577
|
T | A | 1 | a0001c0001t0003g0070 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.666-12998A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457577 | ||||||
| chr2:42457590
|
T | C | 5 | a0001c0001t0002g0326a0001c0001t0008g0088a0001c0001t0008g0089others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-13011A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457590 | ||||||
| chr2:42457617
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0015g0033 | 2 | HG02083.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.666-13038G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457617 | ||||||
| chr2:42457627
|
T | TCA | 43 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0074others(40): Show | 44 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.666-13050_666-1304 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACA | 28 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0085others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-13052_666-1304 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACA | 84 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0075others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.666-13054_666-1304 others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(1): Show |
49 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0223others(46): Show | 49 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.666-13056_666-1304 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(3): Show |
32 | a0001c0001t0001g0188a0001c0001t0001g0205a0001c0001t0001g0238others(29): Show | 32 | HG00323.hp1 HG00733.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.666-13058_666-1304 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(5): Show |
36 | a0001c0001t0001g0093a0001c0001t0001g0139a0001c0001t0001g0199others(33): Show | 36 | HG01074.hp1 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.666-13060_666-1304 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(7): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0245others(6): Show | 10 | HG01106.hp2 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-13062_666-1304 others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(9): Show |
6 | a0001c0001t0001g0058a0001c0001t0001g0286a0001c0001t0002g0225others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-13064_666-1304 others(20): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
T | TCACACAC others(13): Show |
1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.666-13068_666-1304 others(24): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
TCA | T | 6 | a0001c0001t0004g0218a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-13050_666-1304 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
TCACA | T | 10 | a0001c0001t0003g0184a0001c0001t0003g0230a0001c0001t0003g0253others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-13052_666-1304 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
TCACACAC others(1): Show |
T | 25 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0143others(22): Show | 25 | HG00544.hp2 HG02615.hp2 HG02647.hp1 others(22): Show |
intron_variant | MODIFIER | c.666-13056_666-1304 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457627
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0004g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.666-13058_666-1304 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457627 | ||||||
| chr2:42457678
|
C | A | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.666-13099G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457678 | ||||||
| chr2:42457864
|
T | C | 20 | a0001c0001t0001g0132a0001c0001t0004g0092a0001c0001t0004g0137others(17): Show | 20 | HG00544.hp2 HG02602.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.666-13285A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457864 | ||||||
| chr2:42457870
|
C | T | 94 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.666-13291G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457870 | ||||||
| chr2:42457994
|
T | C | 2 | a0001c0001t0010g0133a0001c0001t0010g0333 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.666-13415A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42457994 | ||||||
| chr2:42458202
|
T | C | 5 | a0001c0001t0002g0326a0001c0001t0008g0088a0001c0001t0008g0089others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-13623A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458202 | ||||||
| chr2:42458265
|
C | G | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.666-13686G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458265 | ||||||
| chr2:42458266
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.666-13687C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458266 | ||||||
| chr2:42458337
|
C | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260 | 3 | HG02723.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.666-13758G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458337 | ||||||
| chr2:42458491
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.666-13912A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458491 | ||||||
| chr2:42458802
|
G | GA | 269 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(266): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.666-14224dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458802 | ||||||
| chr2:42458811
|
A | AG | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-14233_666-1423 others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42458811 | ||||||
| chr2:42459184
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-14605C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459184 | ||||||
| chr2:42459199
|
C | CA | 140 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0128others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.666-14621dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459199 | ||||||
| chr2:42459401
|
C | T | 6 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-14822G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459401 | ||||||
| chr2:42459737
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.666-15158C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459737 | ||||||
| chr2:42459758
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.666-15179A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459758 | ||||||
| chr2:42459854
|
T | C | 1 | a0001c0001t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.666-15275A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459854 | ||||||
| chr2:42459901
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.666-15322C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459901 | ||||||
| chr2:42459981
|
G | GA | 235 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0128others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.666-15403dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459981 | ||||||
| chr2:42459981
|
G | GAAA | 37 | a0001c0001t0001g0058a0001c0001t0001g0139a0001c0001t0001g0187others(34): Show | 37 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-15405_666-1540 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42459981 | ||||||
| chr2:42460016
|
G | C | 5 | a0001c0001t0001g0132a0001c0001t0008g0088a0001c0001t0008g0089others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-15437C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460016 | ||||||
| chr2:42460067
|
T | C | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-15488A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460067 | ||||||
| chr2:42460068
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-15489T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460068 | ||||||
| chr2:42460122
|
G | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0002g0138 | 3 | HG02109.hp1 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-15543C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460122 | ||||||
| chr2:42460152
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.666-15573G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460152 | ||||||
| chr2:42460203
|
A | G | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-15624T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460203 | ||||||
| chr2:42460389
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG01109.hp2 HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.666-15810T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460389 | ||||||
| chr2:42460439
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-15860C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460439 | ||||||
| chr2:42460553
|
A | G | 6 | a0001c0001t0002g0326a0001c0002t0005g0012a0001c0002t0005g0013others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-15974T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460553 | ||||||
| chr2:42460634
|
C | G | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.666-16055G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460634 | ||||||
| chr2:42460870
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.666-16291A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460870 | ||||||
| chr2:42460985
|
C | A | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-16406G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460985 | ||||||
| chr2:42460988
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.666-16409G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42460988 | ||||||
| chr2:42461015
|
G | C | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-16436C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461015 | ||||||
| chr2:42461182
|
C | CA | 18 | a0001c0001t0001g0116a0001c0001t0001g0181a0001c0001t0001g0309others(15): Show | 18 | HG00323.hp2 HG02109.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.666-16604dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461182 | ||||||
| chr2:42461182
|
C | CAA | 80 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(77): Show | 81 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.666-16605_666-1660 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461182 | ||||||
| chr2:42461182
|
C | CAAA | 10 | a0001c0001t0003g0021a0001c0001t0003g0037a0001c0001t0003g0054others(7): Show | 10 | HG00621.hp1 HG01123.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-16606_666-1660 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461182 | ||||||
| chr2:42461182
|
CA | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0075others(11): Show | 14 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.666-16604delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461182 | ||||||
| chr2:42461183
|
A | AAAAC | 11 | a0001c0001t0001g0090a0001c0001t0001g0205a0001c0001t0001g0216others(8): Show | 11 | HG02300.hp2 HG02572.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-16605_666-1660 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461183 | ||||||
| chr2:42461184
|
A | AAAC | 35 | a0001c0001t0001g0058a0001c0001t0001g0139a0001c0001t0001g0187others(32): Show | 35 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.666-16606_666-1660 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461184 | ||||||
| chr2:42461185
|
A | AAC | 7 | a0001c0001t0001g0280a0001c0001t0002g0032a0001c0001t0002g0312others(4): Show | 7 | HG00741.hp2 HG01943.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-16607_666-1660 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461185 | ||||||
| chr2:42461186
|
A | AC | 107 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0128others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.666-16608_666-1660 others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461186 | ||||||
| chr2:42461187
|
A | C | 10 | a0001c0001t0001g0019a0001c0001t0002g0235a0001c0001t0002g0322others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-16608T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461187 | ||||||
| chr2:42461188
|
A | C | 7 | a0001c0001t0004g0240a0001c0001t0004g0262a0001c0002t0005g0012others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-16609T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461188 | ||||||
| chr2:42461189
|
A | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0285others(1): Show | 4 | HG01516.hp2 HG01517.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-16610T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461189 | ||||||
| chr2:42461190
|
A | C | 3 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0191 | 3 | HG00738.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.666-16611T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461190 | ||||||
| chr2:42461193
|
A | C | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.666-16614T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461193 | ||||||
| chr2:42461194
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-16615T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461194 | ||||||
| chr2:42461272
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.666-16693C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461272 | ||||||
| chr2:42461550
|
C | A | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-16971G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461550 | ||||||
| chr2:42461657
|
T | C | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0077others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.666-17078A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461657 | ||||||
| chr2:42461672
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.666-17093G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461672 | ||||||
| chr2:42461712
|
G | T | 2 | a0001c0002t0005g0013a0001c0002t0005g0016 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.666-17133C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461712 | ||||||
| chr2:42461770
|
C | T | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-17191G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461770 | ||||||
| chr2:42461794
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260others(1): Show | 4 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-17215A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461794 | ||||||
| chr2:42461852
|
A | T | 1 | a0001c0001t0010g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.666-17273T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461852 | ||||||
| chr2:42461890
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.666-17311A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42461890 | ||||||
| chr2:42462145
|
GTGT | G | 4 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0304others(1): Show | 4 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-17569_666-1756 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462145 | ||||||
| chr2:42462222
|
C | T | 59 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(56): Show | 60 | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.666-17643G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462222 | ||||||
| chr2:42462225
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-17646C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462225 | ||||||
| chr2:42462294
|
C | G | 1 | a0001c0001t0010g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.666-17715G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462294 | ||||||
| chr2:42462498
|
A | G | 4 | a0001c0001t0003g0207a0001c0001t0003g0250a0001c0001t0003g0251others(1): Show | 4 | HG01071.hp1 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-17919T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462498 | ||||||
| chr2:42462617
|
C | G | 279 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0077others(276): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.666-18038G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462617 | ||||||
| chr2:42462661
|
G | A | 11 | a0001c0001t0001g0058a0001c0001t0001g0202a0001c0001t0001g0223others(8): Show | 11 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-18082C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462661 | ||||||
| chr2:42462712
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.666-18133T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462712 | ||||||
| chr2:42462717
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.666-18138G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462717 | ||||||
| chr2:42462802
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-18223C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462802 | ||||||
| chr2:42462882
|
A | AT | 4 | a0001c0001t0001g0139a0001c0001t0002g0311a0001c0001t0003g0071others(1): Show | 4 | NA18951.hp2 NA18952.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-18304dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462882 | ||||||
| chr2:42462934
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.666-18355A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462934 | ||||||
| chr2:42462994
|
T | C | 1 | a0001c0001t0010g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.666-18415A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42462994 | ||||||
| chr2:42463048
|
T | C | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-18469A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463048 | ||||||
| chr2:42463115
|
AAAC | A | 28 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(25): Show | 28 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-18539_666-1853 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463115 | ||||||
| chr2:42463212
|
A | G | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-18633T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463212 | ||||||
| chr2:42463272
|
T | C | 6 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-18693A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463272 | ||||||
| chr2:42463326
|
GTAGTGAG others(9): Show |
G | 285 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0077others(282): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.666-18763_666-1874 others(20): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463326 | ||||||
| chr2:42463345
|
CCTGA | C | 285 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0077others(282): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.666-18770_666-1876 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463345 | ||||||
| chr2:42463504
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.666-18925A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463504 | ||||||
| chr2:42463588
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-19009G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463588 | ||||||
| chr2:42463589
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.666-19010G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463589 | ||||||
| chr2:42463738
|
C | T | 131 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0139others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.666-19159G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463738 | ||||||
| chr2:42463741
|
C | T | 28 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(25): Show | 28 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-19162G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463741 | ||||||
| chr2:42463823
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.666-19244G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463823 | ||||||
| chr2:42463913
|
G | A | 27 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(24): Show | 27 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-19334C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463913 | ||||||
| chr2:42463933
|
C | T | 183 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.666-19354G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463933 | ||||||
| chr2:42463955
|
T | A | 37 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0187others(34): Show | 37 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-19376A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42463955 | ||||||
| chr2:42464081
|
A | G | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.666-19502T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464081 | ||||||
| chr2:42464094
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.666-19515G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464094 | ||||||
| chr2:42464281
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.666-19702C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464281 | ||||||
| chr2:42464403
|
A | T | 1 | a0001c0001t0004g0092 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.666-19824T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464403 | ||||||
| chr2:42464421
|
G | C | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-19842C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464421 | ||||||
| chr2:42464461
|
T | A | 98 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(95): Show | 99 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.666-19882A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464461 | ||||||
| chr2:42464584
|
G | C | 2 | a0001c0001t0004g0086a0001c0001t0021g0087 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.666-20005C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464584 | ||||||
| chr2:42464658
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.666-20079G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464658 | ||||||
| chr2:42464719
|
G | A | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-20140C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464719 | ||||||
| chr2:42464864
|
G | A | 3 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | HG01074.hp1 HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.666-20285C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464864 | ||||||
| chr2:42464914
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.666-20335T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464914 | ||||||
| chr2:42464922
|
A | C | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.666-20343T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464922 | ||||||
| chr2:42464925
|
ACACTATA others(14): Show |
A | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.666-20367_666-2034 others(25): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42464925 | ||||||
| chr2:42465046
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-20467T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465046 | ||||||
| chr2:42465093
|
G | A | 125 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.666-20514C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465093 | ||||||
| chr2:42465119
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.666-20540A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465119 | ||||||
| chr2:42465130
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.666-20551T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465130 | ||||||
| chr2:42465205
|
A | ATTTC | 3 | a0001c0001t0003g0104a0001c0001t0003g0229a0001c0001t0003g0259 | 3 | NA18947.hp1 NA18962.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.666-20630_666-2062 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465205 | ||||||
| chr2:42465221
|
C | CT | 52 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(49): Show | 52 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.666-20643dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465221 | ||||||
| chr2:42465225
|
T | C | 5 | a0001c0001t0003g0072a0001c0001t0003g0104a0001c0001t0003g0229others(2): Show | 5 | HG02523.hp1 NA18947.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-20646A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465225 | ||||||
| chr2:42465270
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-20691C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465270 | ||||||
| chr2:42465373
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.666-20794G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465373 | ||||||
| chr2:42465482
|
G | A | 50 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(47): Show | 50 | HG00609.hp1 HG01099.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.666-20903C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465482 | ||||||
| chr2:42465532
|
A | G | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-20953T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465532 | ||||||
| chr2:42465619
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.666-21040T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465619 | ||||||
| chr2:42465696
|
C | G | 10 | a0001c0001t0001g0139a0001c0001t0002g0272a0001c0001t0002g0300others(7): Show | 10 | HG01928.hp2 HG01943.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-21117G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465696 | ||||||
| chr2:42465767
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260 | 3 | HG02723.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.666-21188G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465767 | ||||||
| chr2:42465769
|
C | A | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.666-21190G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465769 | ||||||
| chr2:42465796
|
A | AT | 8 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-21218dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465796 | ||||||
| chr2:42465890
|
T | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0075others(8): Show | 11 | HG00741.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-21311A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465890 | ||||||
| chr2:42465916
|
C | T | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.666-21337G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42465916 | ||||||
| chr2:42466132
|
A | G | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(335): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.666-21553T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466132 | ||||||
| chr2:42466136
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260others(1): Show | 4 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-21557A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466136 | ||||||
| chr2:42466249
|
T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-21670A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466249 | ||||||
| chr2:42466321
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260others(1): Show | 4 | HG02723.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-21742C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466321 | ||||||
| chr2:42466335
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-21756C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466335 | ||||||
| chr2:42466393
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666-21814C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466393 | ||||||
| chr2:42466518
|
C | A | 1 | a0001c0001t0003g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.666-21939G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466518 | ||||||
| chr2:42466589
|
C | T | 3 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | HG01074.hp1 HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.666-22010G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466589 | ||||||
| chr2:42466721
|
G | T | 2 | a0001c0001t0003g0207a0001c0001t0003g0250 | 2 | HG01255.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.666-22142C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466721 | ||||||
| chr2:42466751
|
T | TC | 124 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0139others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.666-22173dupG | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466751 | ||||||
| chr2:42466753
|
C | CCT | 11 | a0001c0001t0002g0106a0001c0001t0002g0120a0001c0001t0002g0160others(8): Show | 11 | HG00738.hp1 HG01981.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-22175_666-2217 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466753 | ||||||
| chr2:42466754
|
T | C | 1 | a0001c0001t0003g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666-22175A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466754 | ||||||
| chr2:42466773
|
G | C | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666-22194C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466773 | ||||||
| chr2:42466779
|
G | C | 20 | a0001c0001t0001g0139a0001c0001t0002g0106a0001c0001t0002g0220others(17): Show | 20 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-22200C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466779 | ||||||
| chr2:42466912
|
C | G | 92 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(89): Show | 93 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.666-22333G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466912 | ||||||
| chr2:42466919
|
A | G | 32 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0097others(29): Show | 32 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.666-22340T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466919 | ||||||
| chr2:42466941
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666-22362A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42466941 | ||||||
| chr2:42467044
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0001g0260 | 3 | HG02723.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.666-22465G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467044 | ||||||
| chr2:42467048
|
C | T | 2 | a0001c0001t0010g0133a0001c0001t0010g0333 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.666-22469G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467048 | ||||||
| chr2:42467197
|
G | A | 93 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(90): Show | 94 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.666-22618C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467197 | ||||||
| chr2:42467269
|
G | C | 2 | a0001c0001t0008g0088a0001c0001t0008g0089 | 2 | HG01106.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.666-22690C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467269 | ||||||
| chr2:42467333
|
G | A | 92 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(89): Show | 93 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.666-22754C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467333 | ||||||
| chr2:42467366
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0009g0107 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.666-22787T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467366 | ||||||
| chr2:42467485
|
T | C | 1 | a0001c0001t0003g0254 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.666-22906A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467485 | ||||||
| chr2:42467601
|
G | C | 2 | a0001c0001t0002g0326a0001c0001t0003g0332 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.666-23022C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467601 | ||||||
| chr2:42467715
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-23136T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467715 | ||||||
| chr2:42467753
|
T | G | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.666-23174A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467753 | ||||||
| chr2:42467760
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-23181T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467760 | ||||||
| chr2:42467761
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-23182C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467761 | ||||||
| chr2:42467789
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.666-23210C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467789 | ||||||
| chr2:42467797
|
CTT | C | 4 | a0001c0001t0008g0088a0001c0001t0008g0089a0001c0001t0008g0324others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-23220_666-2321 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467797 | ||||||
| chr2:42467893
|
C | T | 36 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0097others(33): Show | 36 | HG00609.hp1 HG01099.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.666-23314G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467893 | ||||||
| chr2:42467896
|
G | A | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-23317C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467896 | ||||||
| chr2:42467970
|
CA | C | 7 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0145others(4): Show | 7 | HG01256.hp2 HG01496.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-23392delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42467970 | ||||||
| chr2:42468534
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.666-23955G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468534 | ||||||
| chr2:42468620
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0002g0146 | 2 | HG01168.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.666-24041A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468620 | ||||||
| chr2:42468739
|
A | G | 96 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.665+24098T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468739 | ||||||
| chr2:42468740
|
G | A | 96 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.665+24097C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468740 | ||||||
| chr2:42468759
|
C | A | 9 | a0001c0001t0002g0106a0001c0001t0002g0220a0001c0001t0002g0221others(6): Show | 9 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+24078G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468759 | ||||||
| chr2:42468815
|
C | A | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+24022G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468815 | ||||||
| chr2:42468832
|
G | A | 96 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.665+24005C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468832 | ||||||
| chr2:42468885
|
C | T | 10 | a0001c0001t0004g0137a0001c0001t0004g0149a0001c0001t0004g0150others(7): Show | 10 | HG00544.hp2 HG02602.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+23952G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468885 | ||||||
| chr2:42468902
|
C | T | 120 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.665+23935G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468902 | ||||||
| chr2:42468954
|
C | CA | 12 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0098others(9): Show | 12 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.665+23882dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468954 | ||||||
| chr2:42468954
|
CA | C | 90 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0304others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.665+23882delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468954 | ||||||
| chr2:42468954
|
CAA | C | 117 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0187others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.665+23881_665+2388 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468954 | ||||||
| chr2:42468954
|
CAAA | C | 54 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(51): Show | 54 | HG00609.hp1 HG01099.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.665+23880_665+2388 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468954 | ||||||
| chr2:42468981
|
AT | A | 4 | a0001c0001t0003g0184a0001c0001t0003g0230a0001c0001t0003g0253others(1): Show | 4 | NA18945.hp1 NA18971.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+23855delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468981 | ||||||
| chr2:42468982
|
T | A | 1 | a0001c0001t0003g0254 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.665+23855A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468982 | ||||||
| chr2:42468991
|
C | T | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+23846G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42468991 | ||||||
| chr2:42469104
|
T | C | 1 | a0001c0001t0003g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.665+23733A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469104 | ||||||
| chr2:42469158
|
C | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0151a0001c0001t0002g0161others(2): Show | 5 | HG00673.hp1 NA18959.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+23679G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469158 | ||||||
| chr2:42469179
|
G | T | 2 | a0001c0002t0005g0013a0001c0002t0005g0016 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.665+23658C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469179 | ||||||
| chr2:42469203
|
G | A | 3 | a0001c0001t0003g0103a0001c0001t0003g0234a0001c0001t0003g0263 | 3 | HG02922.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665+23634C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469203 | ||||||
| chr2:42469255
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+23582T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469255 | ||||||
| chr2:42469327
|
G | T | 1 | a0001c0001t0002g0017 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.665+23510C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469327 | ||||||
| chr2:42469331
|
C | A | 1 | a0001c0001t0004g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.665+23506G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469331 | ||||||
| chr2:42469386
|
G | A | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+23451C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469386 | ||||||
| chr2:42469416
|
C | CA | 13 | a0001c0001t0001g0020a0001c0001t0001g0090a0001c0001t0001g0216others(10): Show | 13 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.665+23420dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469416 | ||||||
| chr2:42469416
|
C | CAA | 31 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(28): Show | 31 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.665+23419_665+2342 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469416 | ||||||
| chr2:42469416
|
C | CAAA | 7 | a0001c0001t0001g0139a0001c0001t0001g0189a0001c0001t0001g0238others(4): Show | 7 | HG00609.hp1 HG01099.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+23418_665+2342 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469416 | ||||||
| chr2:42469416
|
CA | C | 8 | a0001c0001t0001g0299a0001c0001t0002g0123a0001c0001t0002g0131others(5): Show | 8 | HG00323.hp1 HG01070.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+23420delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469416 | ||||||
| chr2:42469715
|
T | C | 96 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.665+23122A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469715 | ||||||
| chr2:42469768
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+23069A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469768 | ||||||
| chr2:42469921
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.665+22916C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469921 | ||||||
| chr2:42469939
|
C | G | 2 | a0001c0001t0010g0133a0001c0001t0010g0333 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.665+22898G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42469939 | ||||||
| chr2:42470057
|
G | A | 120 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.665+22780C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470057 | ||||||
| chr2:42470210
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.665+22627C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470210 | ||||||
| chr2:42470300
|
T | C | 1 | a0001c0001t0003g0254 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.665+22537A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470300 | ||||||
| chr2:42470316
|
A | C | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0321 | 3 | HG01515.hp2 HG01517.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.665+22521T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470316 | ||||||
| chr2:42470385
|
T | C | 8 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+22452A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470385 | ||||||
| chr2:42470430
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+22407C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470430 | ||||||
| chr2:42470436
|
C | A | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+22401G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470436 | ||||||
| chr2:42470448
|
A | C | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+22389T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470448 | ||||||
| chr2:42470454
|
G | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+22383C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470454 | ||||||
| chr2:42470520
|
T | C | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG02109.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.665+22317A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470520 | ||||||
| chr2:42470698
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.665+22139C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470698 | ||||||
| chr2:42470886
|
G | A | 41 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(38): Show | 41 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.665+21951C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470886 | ||||||
| chr2:42470995
|
T | C | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.665+21842A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42470995 | ||||||
| chr2:42471028
|
T | G | 1 | a0001c0001t0002g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.665+21809A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471028 | ||||||
| chr2:42471155
|
A | AGT | 46 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0190others(43): Show | 47 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.665+21680_665+2168 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
A | AGTGT | 44 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(41): Show | 44 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+21678_665+2168 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
A | AGTGTGT | 19 | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0136others(16): Show | 19 | HG00735.hp2 HG01169.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.665+21676_665+2168 others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
A | AGTGTGTG others(1): Show |
69 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0204others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.665+21674_665+2168 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
A | AGTGTGTG others(3): Show |
19 | a0001c0001t0001g0139a0001c0001t0001g0215a0001c0001t0001g0296others(16): Show | 19 | HG00609.hp1 HG01070.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.665+21672_665+2168 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0002g0134a0001c0001t0002g0178a0001c0001t0002g0196others(1): Show | 4 | HG00642.hp1 HG03669.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+21670_665+2168 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
AGT | A | 16 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0187others(13): Show | 16 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.665+21680_665+2168 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471155
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.665+21668_665+2168 others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471155 | ||||||
| chr2:42471182
|
G | A | 20 | a0001c0001t0001g0202a0001c0001t0001g0223a0001c0001t0001g0224others(17): Show | 20 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.665+21655C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471182 | ||||||
| chr2:42471184
|
G | A | 41 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0187others(38): Show | 41 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.665+21653C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471184 | ||||||
| chr2:42471184
|
G | GTA | 4 | a0001c0001t0001g0216a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 4 | HG02109.hp2 HG02723.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+21651_665+2165 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471184 | ||||||
| chr2:42471184
|
G | GTATA | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+21649_665+2165 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471184 | ||||||
| chr2:42471184
|
G | GTGTATA | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG03139.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.665+21652_665+2165 others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471184 | ||||||
| chr2:42471186
|
A | G | 229 | a0001c0001t0001g0030a0001c0001t0001g0084a0001c0001t0001g0098others(226): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.665+21651T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471186 | ||||||
| chr2:42471188
|
A | G | 107 | a0001c0001t0001g0248a0001c0001t0002g0017a0001c0001t0002g0141others(104): Show | 108 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.665+21649T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471188 | ||||||
| chr2:42471190
|
A | G | 6 | a0001c0001t0003g0035a0001c0001t0003g0219a0001c0001t0003g0255others(3): Show | 6 | HG00735.hp2 HG02602.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+21647T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471190 | ||||||
| chr2:42471202
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.665+21635A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471202 | ||||||
| chr2:42471234
|
C | A | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+21603G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471234 | ||||||
| chr2:42471260
|
C | T | 8 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+21577G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471260 | ||||||
| chr2:42471501
|
C | A | 1 | a0001c0001t0008g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.665+21336G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471501 | ||||||
| chr2:42471537
|
G | C | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0330 | 3 | NA18940.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.665+21300C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471537 | ||||||
| chr2:42471806
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.665+21031G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471806 | ||||||
| chr2:42471870
|
C | T | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.665+20967G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471870 | ||||||
| chr2:42471885
|
C | CA | 17 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0001g0247others(14): Show | 17 | HG01099.hp1 HG01243.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+20951dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471885 | ||||||
| chr2:42471885
|
CA | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(65): Show | 70 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.665+20951delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42471885 | ||||||
| chr2:42472024
|
T | C | 126 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.665+20813A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472024 | ||||||
| chr2:42472381
|
T | C | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+20456A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472381 | ||||||
| chr2:42472439
|
G | A | 1 | a0001c0002t0005g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.665+20398C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472439 | ||||||
| chr2:42472503
|
A | AT | 48 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0132others(45): Show | 48 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.665+20333dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472503 | ||||||
| chr2:42472560
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+20277G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472560 | ||||||
| chr2:42472624
|
C | G | 7 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(4): Show | 7 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+20213G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472624 | ||||||
| chr2:42472775
|
C | A | 45 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(42): Show | 45 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.665+20062G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472775 | ||||||
| chr2:42472798
|
A | T | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.665+20039T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472798 | ||||||
| chr2:42472838
|
A | G | 45 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(42): Show | 45 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.665+19999T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472838 | ||||||
| chr2:42472881
|
C | T | 1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.665+19956G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472881 | ||||||
| chr2:42472890
|
G | GAT | 90 | a0001c0001t0001g0248a0001c0001t0002g0167a0001c0001t0002g0195others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.665+19945_665+1994 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472890 | ||||||
| chr2:42472901
|
A | AT | 13 | a0001c0001t0002g0249a0001c0001t0004g0150a0001c0001t0004g0154others(10): Show | 13 | HG00609.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.665+19935dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472901 | ||||||
| chr2:42472902
|
TA | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0190 | 3 | HG00423.hp1 NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.665+19934delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472902 | ||||||
| chr2:42472903
|
A | AT | 69 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0126others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.665+19933dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472903 | ||||||
| chr2:42472903
|
A | ATAT | 10 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0003g0071others(7): Show | 10 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+19933_665+1993 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472903 | ||||||
| chr2:42472903
|
A | ATT | 8 | a0001c0001t0002g0017a0001c0001t0002g0140a0001c0001t0002g0168others(5): Show | 8 | HG01081.hp2 HG01952.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+19932_665+1993 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472903 | ||||||
| chr2:42472903
|
A | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0096a0001c0001t0002g0249others(13): Show | 16 | HG00609.hp1 HG02004.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.665+19934T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472903 | ||||||
| chr2:42472903
|
AT | A | 14 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(11): Show | 14 | HG00323.hp2 HG01106.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+19933delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472903 | ||||||
| chr2:42472904
|
T | TA | 78 | a0001c0001t0001g0058a0001c0001t0001g0132a0001c0001t0001g0139others(75): Show | 78 | HG00099.hp2 HG00733.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.665+19932_665+1993 others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472904 | ||||||
| chr2:42472905
|
T | A | 20 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0001g0197others(17): Show | 20 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.665+19932A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472905 | ||||||
| chr2:42472906
|
T | A | 50 | a0001c0001t0001g0058a0001c0001t0001g0132a0001c0001t0001g0139others(47): Show | 50 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.665+19931A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472906 | ||||||
| chr2:42472907
|
T | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0334a0001c0001t0001g0336 | 3 | HG02109.hp2 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665+19930A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472907 | ||||||
| chr2:42472907
|
T | C | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0321 | 3 | HG01515.hp2 HG01517.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.665+19930A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472907 | ||||||
| chr2:42472908
|
T | A | 6 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0211others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+19929A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472908 | ||||||
| chr2:42472955
|
G | C | 5 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0001g0247others(2): Show | 5 | HG01099.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+19882C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472955 | ||||||
| chr2:42472962
|
C | T | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG01099.hp1 HG01123.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.665+19875G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472962 | ||||||
| chr2:42472978
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.665+19859A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42472978 | ||||||
| chr2:42473005
|
T | C | 289 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(286): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.665+19832A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473005 | ||||||
| chr2:42473058
|
C | G | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+19779G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473058 | ||||||
| chr2:42473059
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+19778C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473059 | ||||||
| chr2:42473063
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665+19774C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473063 | ||||||
| chr2:42473087
|
G | T | 45 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0139others(42): Show | 45 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.665+19750C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473087 | ||||||
| chr2:42473147
|
C | T | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665+19690G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473147 | ||||||
| chr2:42473156
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.665+19681T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473156 | ||||||
| chr2:42473255
|
T | C | 2 | a0001c0001t0003g0234a0001c0001t0003g0263 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665+19582A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473255 | ||||||
| chr2:42473311
|
G | A | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+19526C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473311 | ||||||
| chr2:42473354
|
T | G | 54 | a0001c0001t0001g0058a0001c0001t0001g0139a0001c0001t0001g0187others(51): Show | 54 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.665+19483A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473354 | ||||||
| chr2:42473366
|
T | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0165 | 2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.665+19471A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473366 | ||||||
| chr2:42473385
|
T | A | 1 | a0001c0001t0002g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.665+19452A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473385 | ||||||
| chr2:42473721
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.665+19116T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473721 | ||||||
| chr2:42473741
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG01099.hp1 HG01884.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.665+19096C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473741 | ||||||
| chr2:42473878
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.665+18959C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473878 | ||||||
| chr2:42473965
|
A | T | 127 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0139others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.665+18872T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42473965 | ||||||
| chr2:42474177
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.665+18660C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474177 | ||||||
| chr2:42474202
|
G | A | 36 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG01099.hp1 HG01109.hp2 HG01516.hp2 others(33): Show |
intron_variant | MODIFIER | c.665+18635C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474202 | ||||||
| chr2:42474228
|
G | GA | 4 | a0001c0001t0001g0002a0001c0001t0001g0145a0001c0001t0001g0186others(1): Show | 5 | NA18961.hp1 NA18962.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+18608dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474228 | ||||||
| chr2:42474308
|
A | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+18529T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474308 | ||||||
| chr2:42474336
|
T | C | 96 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.665+18501A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474336 | ||||||
| chr2:42474343
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.665+18494G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474343 | ||||||
| chr2:42474443
|
G | A | 1 | a0001c0001t0011g0004 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.665+18394C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474443 | ||||||
| chr2:42474461
|
C | G | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+18376G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474461 | ||||||
| chr2:42474880
|
TG | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+17956delC | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42474880 | ||||||
| chr2:42475126
|
A | G | 2 | a0001c0001t0003g0234a0001c0001t0003g0263 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665+17711T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475126 | ||||||
| chr2:42475139
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.665+17698C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475139 | ||||||
| chr2:42475323
|
CT | C | 249 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0128others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.665+17513delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475323 | ||||||
| chr2:42475357
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.665+17480C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475357 | ||||||
| chr2:42475453
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.665+17384G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475453 | ||||||
| chr2:42475456
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.665+17381T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475456 | ||||||
| chr2:42475566
|
C | A | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+17271G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475566 | ||||||
| chr2:42475646
|
T | TA | 15 | a0001c0001t0001g0132a0001c0001t0001g0211a0001c0001t0001g0212others(12): Show | 15 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.665+17190dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475646 | ||||||
| chr2:42475646
|
TA | T | 19 | a0001c0001t0001g0102a0001c0001t0001g0126a0001c0001t0001g0128others(16): Show | 19 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.665+17190delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475646 | ||||||
| chr2:42475692
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0247 | 2 | HG01099.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.665+17145A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475692 | ||||||
| chr2:42475742
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.665+17095T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42475742 | ||||||
| chr2:42476032
|
C | A | 1 | a0001c0001t0002g0168 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.665+16805G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476032 | ||||||
| chr2:42476067
|
TATA | T | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+16767_665+1676 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476067 | ||||||
| chr2:42476193
|
C | T | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+16644G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476193 | ||||||
| chr2:42476238
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+16599C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476238 | ||||||
| chr2:42476270
|
G | C | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+16567C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476270 | ||||||
| chr2:42476297
|
C | A | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+16540G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476297 | ||||||
| chr2:42476297
|
C | G | 39 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG01099.hp1 HG01109.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.665+16540G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476297 | ||||||
| chr2:42476487
|
A | T | 122 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0139others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.665+16350T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476487 | ||||||
| chr2:42476499
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.665+16338T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476499 | ||||||
| chr2:42476499
|
AT | A | 8 | a0001c0001t0002g0225a0001c0001t0002g0232a0001c0001t0003g0056others(5): Show | 8 | HG01167.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+16337delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476499 | ||||||
| chr2:42476500
|
T | A | 276 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(273): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.665+16337A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476500 | ||||||
| chr2:42476621
|
G | T | 5 | a0001c0001t0002g0131a0001c0001t0002g0135a0001c0001t0002g0136others(2): Show | 5 | HG01993.hp1 HG02004.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+16216C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476621 | ||||||
| chr2:42476679
|
G | A | 1 | a0001c0001t0013g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.665+16158C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476679 | ||||||
| chr2:42476710
|
G | A | 5 | a0001c0001t0003g0003a0001c0001t0003g0091a0001c0001t0003g0288others(2): Show | 6 | NA18954.hp2 NA18964.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+16127C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476710 | ||||||
| chr2:42476721
|
C | A | 81 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(78): Show | 82 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.665+16116G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476721 | ||||||
| chr2:42476770
|
G | A | 8 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+16067C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476770 | ||||||
| chr2:42476802
|
T | C | 47 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0187others(44): Show | 47 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.665+16035A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476802 | ||||||
| chr2:42476848
|
T | C | 47 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0187others(44): Show | 47 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.665+15989A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476848 | ||||||
| chr2:42476982
|
G | C | 10 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+15855C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42476982 | ||||||
| chr2:42477031
|
A | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0190 | 3 | HG00423.hp1 NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.665+15806T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477031 | ||||||
| chr2:42477124
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.665+15713C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477124 | ||||||
| chr2:42477178
|
C | CA | 5 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0191others(2): Show | 5 | HG00738.hp2 HG02559.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+15658dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477178 | ||||||
| chr2:42477283
|
A | C | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+15554T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477283 | ||||||
| chr2:42477382
|
T | C | 1 | a0001c0001t0003g0026 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.665+15455A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TAC | 6 | a0001c0001t0003g0028a0001c0001t0003g0104a0001c0001t0003g0105others(3): Show | 6 | HG01255.hp1 HG03688.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+15454_665+1545 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACAC | 3 | a0001c0001t0003g0207a0001c0001t0003g0252a0001c0001t0003g0253 | 3 | HG02083.hp1 HG04184.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.665+15454_665+1545 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACACAC | 6 | a0001c0001t0003g0251a0001c0001t0003g0254a0001c0001t0003g0257others(3): Show | 6 | HG01071.hp1 HG02165.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+15454_665+1545 others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0248a0001c0001t0003g0072a0001c0001t0003g0193others(1): Show | 4 | HG00621.hp2 HG02523.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+15454_665+1545 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACACACA others(3): Show |
2 | a0001c0001t0003g0070a0001c0001t0003g0259 | 2 | HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.665+15454_665+1545 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACACACA others(5): Show |
1 | a0001c0001t0003g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.665+15454_665+1545 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477382
|
T | TACACACA others(7): Show |
5 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0003g0228others(2): Show | 5 | NA18940.hp2 NA18947.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+15454_665+1545 others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477382 | ||||||
| chr2:42477384
|
T | C | 34 | a0001c0001t0001g0248a0001c0001t0002g0177a0001c0001t0003g0026others(31): Show | 34 | HG00544.hp1 HG00621.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.665+15453A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TAC | 13 | a0001c0001t0003g0022a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 13 | HG02135.hp1 HG02165.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.665+15452_665+1545 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACAC | 5 | a0001c0001t0003g0038a0001c0001t0003g0052a0001c0001t0003g0069others(2): Show | 5 | NA18951.hp1 NA18964.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+15452_665+1545 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACACAC | 31 | a0001c0001t0001g0128a0001c0001t0002g0110a0001c0001t0002g0136others(28): Show | 31 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.665+15452_665+1545 others(10): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACACACA others(1): Show |
10 | a0001c0001t0002g0119a0001c0001t0002g0144a0001c0001t0002g0146others(7): Show | 10 | HG01981.hp2 HG02293.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+15452_665+1545 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACACACA others(3): Show |
7 | a0001c0001t0002g0120a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 7 | HG00621.hp1 HG02055.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+15452_665+1545 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACACACA others(5): Show |
2 | a0001c0001t0002g0191a0001c0001t0003g0068 | 2 | HG00738.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.665+15452_665+1545 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
T | TACACACA others(7): Show |
1 | a0001c0001t0003g0332 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.665+15452_665+1545 others(18): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477384
|
TATATACA others(5): Show |
T | 1 | a0001c0001t0002g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.665+15441_665+1545 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477384 | ||||||
| chr2:42477385
|
AT | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0199a0001c0001t0001g0216others(4): Show | 7 | HG02723.hp1 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+15451delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477385 | ||||||
| chr2:42477385
|
ATAT | A | 38 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(35): Show | 38 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.665+15449_665+1545 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477385 | ||||||
| chr2:42477386
|
T | C | 227 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0139others(224): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.665+15451A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477386 | ||||||
| chr2:42477388
|
T | C | 231 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0132others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.665+15449A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
T | TAC | 13 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0081others(10): Show | 13 | HG00423.hp1 HG00639.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.665+15447_665+1544 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
T | TACAC | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(20): Show | 25 | HG00099.hp1 HG00609.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+15445_665+1544 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+15437_665+1544 others(16): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
T | TATACACA others(1): Show |
3 | a0001c0001t0007g0268a0001c0001t0007g0284a0001c0001t0007g0331 | 3 | HG02451.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.665+15448_665+1544 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
TACAC | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0208a0001c0001t0001g0317 | 3 | HG01928.hp1 HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.665+15445_665+1544 others(8): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477388
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.665+15439_665+1544 others(14): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477388 | ||||||
| chr2:42477390
|
C | T | 38 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(35): Show | 38 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.665+15447G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477390 | ||||||
| chr2:42477416
|
C | G | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+15421G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477416 | ||||||
| chr2:42477418
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.665+15419G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477418 | ||||||
| chr2:42477420
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0002g0312 | 2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.665+15417G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477420 | ||||||
| chr2:42477422
|
C | CAGACACA others(1): Show |
7 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0002t0005g0012others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+15414_665+1541 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477422 | ||||||
| chr2:42477422
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0002g0322a0001c0001t0004g0137others(11): Show | 14 | HG01106.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+15415G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477422 | ||||||
| chr2:42477424
|
T | C | 144 | a0001c0001t0001g0030a0001c0001t0001g0139a0001c0001t0001g0203others(141): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.665+15413A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477424 | ||||||
| chr2:42477426
|
T | C | 125 | a0001c0001t0001g0030a0001c0001t0001g0204a0001c0001t0001g0248others(122): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.665+15411A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477426 | ||||||
| chr2:42477426
|
TA | T | 43 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG01099.hp1 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.665+15410delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477426 | ||||||
| chr2:42477427
|
A | AT | 6 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0001g0215others(3): Show | 6 | HG01496.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+15409dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477427 | ||||||
| chr2:42477427
|
A | T | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665+15410T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477427 | ||||||
| chr2:42477427
|
AT | A | 58 | a0001c0001t0001g0128a0001c0001t0001g0280a0001c0001t0001g0296others(55): Show | 58 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.665+15409delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477427 | ||||||
| chr2:42477427
|
ATTT | A | 12 | a0001c0001t0001g0132a0001c0001t0002g0172a0001c0001t0002g0173others(9): Show | 12 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+15407_665+1540 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477427 | ||||||
| chr2:42477427
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0060others(3): Show | 6 | HG01167.hp1 HG03669.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+15402_665+1540 others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477427 | ||||||
| chr2:42477428
|
T | C | 74 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(71): Show | 75 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.665+15409A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477428 | ||||||
| chr2:42477428
|
T | TA | 18 | a0001c0001t0001g0203a0001c0001t0001g0212a0001c0001t0001g0214others(15): Show | 18 | HG00544.hp2 HG00741.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.665+15408_665+1540 others(5): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477428 | ||||||
| chr2:42477428
|
T | TATA | 40 | a0001c0001t0001g0030a0001c0001t0001g0139a0001c0001t0001g0204others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.665+15408_665+1540 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477428 | ||||||
| chr2:42477429
|
T | A | 82 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0248others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.665+15408A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477429 | ||||||
| chr2:42477430
|
T | A | 110 | a0001c0001t0001g0030a0001c0001t0001g0139a0001c0001t0001g0203others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.665+15407A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477430 | ||||||
| chr2:42477430
|
T | C | 51 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(48): Show | 52 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.665+15407A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477430 | ||||||
| chr2:42477431
|
T | A | 83 | a0001c0001t0001g0248a0001c0001t0002g0119a0001c0001t0002g0120others(80): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.665+15406A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477431 | ||||||
| chr2:42477433
|
T | A | 83 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(80): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.665+15404A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477433 | ||||||
| chr2:42477435
|
T | A | 86 | a0001c0001t0001g0248a0001c0001t0002g0129a0001c0001t0002g0130others(83): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.665+15402A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477435 | ||||||
| chr2:42477437
|
T | A | 84 | a0001c0001t0001g0248a0001c0001t0003g0003a0001c0001t0003g0021others(81): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.665+15400A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477437 | ||||||
| chr2:42477439
|
T | A | 1 | a0001c0001t0003g0193 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.665+15398A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477439 | ||||||
| chr2:42477459
|
G | C | 2 | a0001c0001t0003g0055a0001c0001t0003g0065 | 2 | HG02523.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.665+15378C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477459 | ||||||
| chr2:42477488
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0002g0146 | 2 | HG01168.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.665+15349G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477488 | ||||||
| chr2:42477617
|
A | G | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+15220T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477617 | ||||||
| chr2:42477676
|
C | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0196 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.665+15161G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477676 | ||||||
| chr2:42477891
|
TA | T | 10 | a0001c0001t0002g0271a0001c0001t0002g0273a0001c0001t0002g0274others(7): Show | 10 | HG00733.hp2 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.665+14945delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477891 | ||||||
| chr2:42477893
|
TA | T | 267 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(264): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.665+14943delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477893 | ||||||
| chr2:42477894
|
A | T | 11 | a0001c0001t0001g0266a0001c0001t0002g0271a0001c0001t0002g0273others(8): Show | 11 | HG00733.hp2 HG01081.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+14943T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477894 | ||||||
| chr2:42477894
|
AT | A | 7 | a0001c0001t0001g0260a0001c0001t0003g0263a0001c0001t0007g0267others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+14942delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42477894 | ||||||
| chr2:42478034
|
G | A | 1 | a0001c0002t0005g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.665+14803C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478034 | ||||||
| chr2:42478091
|
T | C | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | NA18952.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.665+14746A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478091 | ||||||
| chr2:42478142
|
C | G | 284 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.665+14695G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478142 | ||||||
| chr2:42478161
|
A | G | 5 | a0001c0001t0007g0267a0001c0001t0007g0268a0001c0001t0007g0283others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+14676T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478161 | ||||||
| chr2:42478194
|
T | C | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.665+14643A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478194 | ||||||
| chr2:42478227
|
A | T | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665+14610T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478227 | ||||||
| chr2:42478259
|
A | G | 1 | a0001c0001t0014g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.665+14578T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478259 | ||||||
| chr2:42478410
|
T | A | 1 | a0001c0001t0012g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.665+14427A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478410 | ||||||
| chr2:42478420
|
G | A | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+14417C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478420 | ||||||
| chr2:42478436
|
G | A | 125 | a0001c0001t0001g0030a0001c0001t0001g0128a0001c0001t0001g0203others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.665+14401C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478436 | ||||||
| chr2:42478454
|
C | A | 59 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(56): Show | 60 | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.665+14383G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478454 | ||||||
| chr2:42478495
|
T | G | 274 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0090others(271): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.665+14342A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478495 | ||||||
| chr2:42478748
|
G | A | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665+14089C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478748 | ||||||
| chr2:42478872
|
A | G | 2 | a0001c0001t0010g0133a0001c0001t0010g0333 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.665+13965T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478872 | ||||||
| chr2:42478930
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.665+13907C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478930 | ||||||
| chr2:42478956
|
AT | A | 23 | a0001c0001t0001g0090a0001c0001t0001g0116a0001c0001t0001g0216others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.665+13880delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478956 | ||||||
| chr2:42478956
|
ATT | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.665+13879_665+1388 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478956 | ||||||
| chr2:42478956
|
ATTT | A | 45 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0186others(42): Show | 45 | HG00738.hp2 HG01099.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.665+13878_665+1388 others(7): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478956 | ||||||
| chr2:42478985
|
G | A | 5 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(2): Show | 5 | HG02109.hp2 HG02559.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+13852C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42478985 | ||||||
| chr2:42479255
|
C | G | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+13582G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479255 | ||||||
| chr2:42479521
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+13316A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479521 | ||||||
| chr2:42479605
|
C | A | 1 | a0001c0001t0003g0064 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.665+13232G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479605 | ||||||
| chr2:42479645
|
C | CA | 24 | a0001c0001t0001g0090a0001c0001t0001g0190a0001c0001t0001g0197others(21): Show | 24 | HG00738.hp2 HG01192.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.665+13191dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479645 | ||||||
| chr2:42479645
|
CA | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0238a0001c0001t0001g0248others(3): Show | 6 | HG01099.hp1 HG01884.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+13191delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479645 | ||||||
| chr2:42479661
|
G | T | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.665+13176C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479661 | ||||||
| chr2:42479671
|
T | G | 40 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0211others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.665+13166A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479671 | ||||||
| chr2:42479771
|
G | A | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+13066C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479771 | ||||||
| chr2:42479784
|
G | A | 1 | a0001c0001t0002g0194 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.665+13053C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479784 | ||||||
| chr2:42479809
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.665+13028T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479809 | ||||||
| chr2:42479826
|
C | T | 4 | a0001c0001t0002g0141a0001c0001t0002g0143a0001c0001t0002g0144others(1): Show | 4 | NA19012.hp1 NA19065.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+13011G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479826 | ||||||
| chr2:42479873
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.665+12964C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479873 | ||||||
| chr2:42479997
|
C | A | 84 | a0001c0001t0001g0216a0001c0001t0001g0233a0001c0001t0001g0238others(81): Show | 85 | HG00544.hp1 HG00609.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.665+12840G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42479997 | ||||||
| chr2:42480086
|
C | T | 1 | a0001c0001t0004g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.665+12751G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480086 | ||||||
| chr2:42480159
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0296 | 2 | HG01192.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.665+12678A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480159 | ||||||
| chr2:42480214
|
C | T | 24 | a0001c0001t0001g0139a0001c0001t0001g0301a0001c0001t0001g0302others(21): Show | 24 | HG00099.hp2 HG00642.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.665+12623G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480214 | ||||||
| chr2:42480220
|
G | C | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+12617C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480220 | ||||||
| chr2:42480241
|
G | GAT | 26 | a0001c0001t0001g0139a0001c0001t0001g0301a0001c0001t0001g0302others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.665+12595_665+1259 others(6): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480241 | ||||||
| chr2:42480348
|
G | C | 11 | a0001c0001t0001g0317a0001c0001t0002g0300a0001c0001t0002g0311others(8): Show | 11 | HG01928.hp2 HG01943.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+12489C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480348 | ||||||
| chr2:42480392
|
G | A | 6 | a0001c0001t0003g0060a0001c0001t0003g0061a0001c0001t0003g0062others(3): Show | 6 | NA18946.hp1 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+12445C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480392 | ||||||
| chr2:42480414
|
C | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+12423G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480414 | ||||||
| chr2:42480541
|
T | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+12296A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480541 | ||||||
| chr2:42480610
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.665+12227C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480610 | ||||||
| chr2:42480617
|
C | A | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.665+12220G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480617 | ||||||
| chr2:42480618
|
G | A | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+12219C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480618 | ||||||
| chr2:42480655
|
A | G | 5 | a0001c0002t0005g0012a0001c0002t0005g0013a0001c0002t0005g0014others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+12182T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480655 | ||||||
| chr2:42480758
|
T | TA | 11 | a0001c0001t0002g0292a0001c0001t0003g0065a0001c0001t0003g0066others(8): Show | 11 | HG01952.hp1 HG01981.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.665+12078dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480758 | ||||||
| chr2:42480758
|
TA | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(144): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.665+12078delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480758 | ||||||
| chr2:42480848
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665+11989T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480848 | ||||||
| chr2:42480898
|
A | T | 1 | a0001c0001t0002g0140 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.665+11939T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480898 | ||||||
| chr2:42480960
|
T | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.665+11877A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42480960 | ||||||
| chr2:42481034
|
C | G | 1 | a0001c0001t0002g0311 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.665+11803G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481034 | ||||||
| chr2:42481095
|
C | A | 2 | a0001c0001t0003g0263a0001c0001t0004g0262 | 2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.665+11742G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481095 | ||||||
| chr2:42481107
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.665+11730C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481107 | ||||||
| chr2:42481127
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(218): Show | 224 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.665+11710A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481127 | ||||||
| chr2:42481146
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG01123.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+11691C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481146 | ||||||
| chr2:42481154
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.665+11683C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481154 | ||||||
| chr2:42481182
|
T | C | 6 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+11655A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481182 | ||||||
| chr2:42481245
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.665+11592C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481245 | ||||||
| chr2:42481265
|
G | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(243): Show | 249 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.665+11572C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481265 | ||||||
| chr2:42481369
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.665+11468C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481369 | ||||||
| chr2:42481462
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.665+11375G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481462 | ||||||
| chr2:42481701
|
C | T | 2 | a0001c0001t0008g0324a0001c0001t0008g0325 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.665+11136G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481701 | ||||||
| chr2:42481702
|
G | A | 2 | a0001c0001t0006g0008a0001c0001t0006g0009 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665+11135C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481702 | ||||||
| chr2:42481714
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+11123C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481714 | ||||||
| chr2:42481785
|
C | T | 1 | a0001c0001t0002g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.665+11052G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481785 | ||||||
| chr2:42481819
|
G | T | 1 | a0001c0001t0004g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.665+11018C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481819 | ||||||
| chr2:42481872
|
T | C | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665+10965A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481872 | ||||||
| chr2:42481886
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.665+10951A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481886 | ||||||
| chr2:42481983
|
T | C | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+10854A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481983 | ||||||
| chr2:42481996
|
G | T | 8 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+10841C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42481996 | ||||||
| chr2:42482107
|
T | C | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.665+10730A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482107 | ||||||
| chr2:42482108
|
G | C | 1 | a0001c0001t0002g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.665+10729C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482108 | ||||||
| chr2:42482123
|
A | C | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+10714T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482123 | ||||||
| chr2:42482219
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+10618C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482219 | ||||||
| chr2:42482315
|
A | G | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+10522T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482315 | ||||||
| chr2:42482348
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.665+10489C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482348 | ||||||
| chr2:42482462
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.665+10375G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482462 | ||||||
| chr2:42482509
|
G | C | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+10328C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482509 | ||||||
| chr2:42482580
|
G | A | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.665+10257C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482580 | ||||||
| chr2:42482603
|
C | T | 100 | a0001c0001t0001g0216a0001c0001t0001g0223a0001c0001t0001g0224others(97): Show | 101 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.665+10234G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482603 | ||||||
| chr2:42482618
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.665+10219T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482618 | ||||||
| chr2:42482636
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.665+10201G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482636 | ||||||
| chr2:42482654
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.665+10183C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482654 | ||||||
| chr2:42482685
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+10152G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482685 | ||||||
| chr2:42482710
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.665+10127G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482710 | ||||||
| chr2:42482739
|
C | A | 1 | a0001c0001t0010g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665+10098G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482739 | ||||||
| chr2:42482790
|
A | T | 1 | a0001c0001t0003g0026 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.665+10047T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482790 | ||||||
| chr2:42482903
|
T | G | 1 | a0001c0001t0002g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.665+9934A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482903 | ||||||
| chr2:42482924
|
C | T | 34 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0073others(31): Show | 34 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.665+9913G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482924 | ||||||
| chr2:42482983
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0002g0322 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.665+9854G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42482983 | ||||||
| chr2:42483119
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665+9718A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483119 | ||||||
| chr2:42483158
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.665+9679A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483158 | ||||||
| chr2:42483171
|
T | G | 1 | a0001c0001t0003g0067 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.665+9666A>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483171 | ||||||
| chr2:42483196
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.665+9641G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483196 | ||||||
| chr2:42483295
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(100): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.665+9542G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483295 | ||||||
| chr2:42483352
|
T | C | 105 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0223others(102): Show | 106 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.665+9485A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483352 | ||||||
| chr2:42483424
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(335): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.665+9413A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483424 | ||||||
| chr2:42483429
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.665+9408A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483429 | ||||||
| chr2:42483438
|
T | C | 1 | a0001c0001t0006g0010 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.665+9399A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483438 | ||||||
| chr2:42483614
|
G | A | 1 | a0001c0001t0018g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.665+9223C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483614 | ||||||
| chr2:42483702
|
A | G | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+9135T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483702 | ||||||
| chr2:42483723
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.665+9114C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483723 | ||||||
| chr2:42483898
|
C | T | 33 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0073others(30): Show | 33 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.665+8939G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483898 | ||||||
| chr2:42483922
|
C | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(254): Show | 260 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.665+8915G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483922 | ||||||
| chr2:42483951
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(105): Show | 110 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.665+8886G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483951 | ||||||
| chr2:42483979
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(105): Show | 110 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.665+8858G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483979 | ||||||
| chr2:42483980
|
G | A | 113 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0216others(110): Show | 114 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(111): Show |
intron_variant | MODIFIER | c.665+8857C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42483980 | ||||||
| chr2:42484119
|
A | G | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+8718T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484119 | ||||||
| chr2:42484279
|
T | A | 105 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0223others(102): Show | 106 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.665+8558A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484279 | ||||||
| chr2:42484293
|
C | G | 3 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0069 | 3 | NA18966.hp2 NA18991.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.665+8544G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484293 | ||||||
| chr2:42484411
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.665+8426C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484411 | ||||||
| chr2:42484416
|
C | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+8421G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484416 | ||||||
| chr2:42484459
|
T | C | 105 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0223others(102): Show | 106 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.665+8378A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484459 | ||||||
| chr2:42484508
|
G | GTA | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+8327_665+8328d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484508 | ||||||
| chr2:42484533
|
T | A | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.665+8304A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484533 | ||||||
| chr2:42484682
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0075others(1): Show | 4 | HG00741.hp1 HG01243.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+8155G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484682 | ||||||
| chr2:42484752
|
T | C | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+8085A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484752 | ||||||
| chr2:42484928
|
G | C | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.665+7909C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42484928 | ||||||
| chr2:42485098
|
G | T | 1 | a0001c0001t0002g0232 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.665+7739C>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485098 | ||||||
| chr2:42485449
|
A | AT | 102 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0223others(99): Show | 103 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.665+7387dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485449 | ||||||
| chr2:42485449
|
AT | A | 23 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0304others(20): Show | 23 | HG00099.hp2 HG00323.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.665+7387delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485449 | ||||||
| chr2:42485521
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(216): Show | 222 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.665+7316G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485521 | ||||||
| chr2:42485608
|
C | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01928.hp1 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+7229G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485608 | ||||||
| chr2:42485649
|
C | T | 1 | a0001c0001t0004g0137 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.665+7188G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485649 | ||||||
| chr2:42485650
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.665+7187C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485650 | ||||||
| chr2:42485695
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.665+7142C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485695 | ||||||
| chr2:42485792
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(97): Show | 102 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.665+7045C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485792 | ||||||
| chr2:42485839
|
A | T | 1 | a0001c0001t0003g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.665+6998T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42485839 | ||||||
| chr2:42486139
|
C | G | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0002g0220others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+6698G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486139 | ||||||
| chr2:42486148
|
G | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG00735.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.665+6689C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486148 | ||||||
| chr2:42486210
|
C | T | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0002g0220others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+6627G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486210 | ||||||
| chr2:42486338
|
C | T | 1 | a0001c0001t0002g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.665+6499G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486338 | ||||||
| chr2:42486516
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.665+6321G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486516 | ||||||
| chr2:42486589
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+6248C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486589 | ||||||
| chr2:42486819
|
C | T | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+6018G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486819 | ||||||
| chr2:42486824
|
G | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG00735.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.665+6013C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486824 | ||||||
| chr2:42486920
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.665+5917T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42486920 | ||||||
| chr2:42487018
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.665+5819T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487018 | ||||||
| chr2:42487112
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0010g0133 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.665+5725C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487112 | ||||||
| chr2:42487156
|
C | CA | 71 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0075others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.665+5680dupT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487156 | ||||||
| chr2:42487156
|
CA | C | 6 | a0001c0001t0001g0132a0001c0001t0001g0297a0001c0001t0003g0230others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+5680delT | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487156 | ||||||
| chr2:42487243
|
A | G | 32 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0073others(29): Show | 32 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.665+5594T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487243 | ||||||
| chr2:42487259
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0002g0322 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.665+5578A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487259 | ||||||
| chr2:42487347
|
CT | C | 60 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0001g0074others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.665+5489delA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487347 | ||||||
| chr2:42487347
|
CTT | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0102others(214): Show | 220 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.665+5488_665+5489d others(4): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487347 | ||||||
| chr2:42487353
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+5484A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487353 | ||||||
| chr2:42487491
|
A | G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0002g0220others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+5346T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487491 | ||||||
| chr2:42487660
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665+5177T>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487660 | ||||||
| chr2:42487667
|
A | G | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+5170T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487667 | ||||||
| chr2:42487685
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665+5152A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487685 | ||||||
| chr2:42487771
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.665+5066G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487771 | ||||||
| chr2:42487782
|
C | G | 1 | a0001c0001t0002g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.665+5055G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487782 | ||||||
| chr2:42487875
|
C | A | 2 | a0001c0001t0003g0103a0001c0004t0001g0338 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.665+4962G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487875 | ||||||
| chr2:42487897
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.665+4940G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487897 | ||||||
| chr2:42487995
|
T | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0105 | 2 | NA18947.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.665+4842A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42487995 | ||||||
| chr2:42488068
|
A | G | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+4769T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488068 | ||||||
| chr2:42488071
|
A | C | 1 | a0001c0001t0002g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.665+4766T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488071 | ||||||
| chr2:42488445
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(99): Show | 104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.665+4392C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488445 | ||||||
| chr2:42488552
|
C | CT | 6 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 7 | HG01168.hp1 HG02135.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+4284dupA | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488552 | ||||||
| chr2:42488618
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.665+4219G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488618 | ||||||
| chr2:42488720
|
T | C | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665+4117A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488720 | ||||||
| chr2:42488801
|
C | T | 1 | a0001c0001t0013g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.665+4036G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488801 | ||||||
| chr2:42488884
|
T | C | 2 | a0001c0001t0007g0267a0001c0001t0007g0268 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.665+3953A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488884 | ||||||
| chr2:42488890
|
T | C | 1 | a0001c0004t0001g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.665+3947A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488890 | ||||||
| chr2:42488993
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.665+3844C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42488993 | ||||||
| chr2:42489030
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665+3807G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489030 | ||||||
| chr2:42489171
|
T | C | 32 | a0001c0001t0001g0202a0001c0001t0001g0208a0001c0001t0001g0270others(29): Show | 33 | HG00733.hp2 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.665+3666A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489171 | ||||||
| chr2:42489185
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.665+3652C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489185 | ||||||
| chr2:42489199
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.665+3638C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489199 | ||||||
| chr2:42489311
|
C | G | 28 | a0001c0001t0001g0215a0001c0001t0001g0301a0001c0001t0001g0302others(25): Show | 28 | HG00099.hp2 HG00323.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.665+3526G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489311 | ||||||
| chr2:42489481
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0116others(105): Show | 110 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.665+3356T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489481 | ||||||
| chr2:42489489
|
G | A | 1 | a0001c0001t0003g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.665+3348C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489489 | ||||||
| chr2:42489523
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0116others(91): Show | 96 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.665+3314G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489523 | ||||||
| chr2:42489574
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.665+3263G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489574 | ||||||
| chr2:42489696
|
GTAAGGGA others(3): Show |
G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0116others(93): Show | 98 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.665+3131_665+3140d others(12): Show |
KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489696 | ||||||
| chr2:42489717
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.665+3120G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489717 | ||||||
| chr2:42489740
|
C | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.665+3097G>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489740 | ||||||
| chr2:42489844
|
T | C | 29 | a0001c0001t0001g0215a0001c0001t0001g0301a0001c0001t0001g0302others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.665+2993A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489844 | ||||||
| chr2:42489875
|
A | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0116others(98): Show | 103 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.665+2962T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489875 | ||||||
| chr2:42489978
|
C | G | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+2859G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489978 | ||||||
| chr2:42489999
|
C | T | 6 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+2838G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42489999 | ||||||
| chr2:42490165
|
C | G | 1 | a0001c0001t0003g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665+2672G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42490165 | ||||||
| chr2:42490302
|
G | A | 2 | a0001c0001t0008g0324a0001c0001t0008g0325 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.665+2535C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42490302 | ||||||
| chr2:42490811
|
A | C | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+2026T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42490811 | ||||||
| chr2:42490889
|
T | C | 1 | a0001c0005t0004g0339 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.665+1948A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42490889 | ||||||
| chr2:42490903
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+1934C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42490903 | ||||||
| chr2:42491066
|
T | A | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02622.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+1771A>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491066 | ||||||
| chr2:42491141
|
C | G | 2 | a0001c0001t0004g0217a0001c0001t0004g0218 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.665+1696G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491141 | ||||||
| chr2:42491261
|
A | G | 1 | a0001c0002t0005g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+1576T>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491261 | ||||||
| chr2:42491271
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.665+1566T>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491271 | ||||||
| chr2:42491285
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665+1552G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491285 | ||||||
| chr2:42491377
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+1460G>C | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491377 | ||||||
| chr2:42491758
|
G | A | 133 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0223others(130): Show | 134 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.665+1079C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491758 | ||||||
| chr2:42491800
|
G | A | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665+1037C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42491800 | ||||||
| chr2:42492016
|
G | C | 1 | a0001c0001t0003g0327 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665+821C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492016 | ||||||
| chr2:42492181
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0116others(236): Show | 242 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.665+656A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492181 | ||||||
| chr2:42492267
|
G | C | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG02109.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.665+570C>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492267 | ||||||
| chr2:42492386
|
G | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0330 | 3 | NA18940.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.665+451C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492386 | ||||||
| chr2:42492476
|
G | A | 1 | a0001c0005t0004g0339 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.665+361C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492476 | ||||||
| chr2:42492607
|
C | T | 1 | a0001c0003t0001g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665+230G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492607 | ||||||
| chr2:42492630
|
G | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0330 | 3 | NA18940.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.665+207C>T | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492630 | ||||||
| chr2:42492707
|
T | TG | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(335): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.665+129dupC | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492707 | ||||||
| chr2:42492720
|
G | GC | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(335): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.665+116dupG | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492720 | ||||||
| chr2:42492812
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.665+25G>A | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492812 | ||||||
| chr2:42492816
|
T | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+21A>G | KCNG3 | ENSG00000171126.8 | transcript | ENST00000306078.2 | protein_coding | 1/1 | chr2 | 42492816 |