Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23235 |
|---|---|
| ensemblid | ENSG00000170145.5 |
| hgncid | 21680 |
| symbol | SIK2 |
| name | salt inducible kinase 2 |
| refseq_nuc | NM_015191.3 |
| refseq_prot | NP_056006.1 |
| ensembl_nuc | ENST00000304987.4 |
| ensembl_prot | ENSP00000305976.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 111602449 |
| end | 111730855 |
| strand | + |
| ver | v1.2 |
| region | chr11:111602449-111730855 |
| region5000 | chr11:111597449-111735855 |
| regionname0 | SIK2_chr11_111602449_111730855 |
| regionname5000 | SIK2_chr11_111597449_111735855 |
| 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 | 926 | 197 | 85 | 50 | 38 | 10 | 12 | 24 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0002 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| 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 | 2781 | 191 | 82 | 48 | 38 | 9 | 12 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0002 | 0/0 | 2781 | 2 | 0 | 1 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0003 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0004 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0005 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0006 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| c0007 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6841 | 34 | 8 | 7 | 14 | 1 | 4 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0002 | 0/1 | 6841 | 19 | 1 | 4 | 8 | 2 | 3 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0003 | 0/0 | 6841 | 15 | 3 | 5 | 3 | 2 | 2 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0004 | 0/0 | 6839 | 12 | 11 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0005 | 1/0 | 6842 | 11 | 8 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0006 | 0/0 | 6841 | 8 | 0 | 5 | 3 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0007 | 0/0 | 6841 | 8 | 8 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0008 | 0/0 | 6841 | 8 | 5 | 3 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0009 | 0/0 | 6841 | 6 | 5 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0010 | 0/0 | 6821 | 5 | 5 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0011 | 0/0 | 6841 | 5 | 1 | 2 | 0 | 2 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0012 | 0/0 | 6841 | 4 | 1 | 1 | 1 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0013 | 0/0 | 6841 | 3 | 0 | 3 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0014 | 0/0 | 6828 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0015 | 0/0 | 6841 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0016 | 0/0 | 6821 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0017 | 0/0 | 6842 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0018 | 0/0 | 6840 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0019 | 0/0 | 6841 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0020 | 0/0 | 6843 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0021 | 0/0 | 6842 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0022 | 0/0 | 6841 | 2 | 0 | 0 | 2 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0023 | 0/0 | 6841 | 2 | 1 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0024 | 0/0 | 6840 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0025 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0026 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0027 | 0/0 | 6842 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0028 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0029 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0030 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0031 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0032 | 0/0 | 6821 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0033 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0034 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0035 | 0/0 | 6842 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0036 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0037 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0038 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0039 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0040 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0041 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0042 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0043 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0044 | 0/0 | 6842 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0045 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0046 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0047 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0048 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0049 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0050 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0051 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0052 | 0/0 | 6820 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0053 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0054 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0055 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0056 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0057 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0058 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0059 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0060 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0061 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0062 | 0/0 | 6842 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| t0063 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| 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 | 2781 | 191 | 82 | 48 | 38 | 9 | 12 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0002 | 0/0 | 2781 | 2 | 0 | 1 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0003 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0004 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0006 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0007 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0002c0005 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9621 | 33 | 7 | 7 | 14 | 1 | 4 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0002 | 0/1 | 9621 | 19 | 1 | 4 | 8 | 2 | 3 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0003 | 0/0 | 9621 | 13 | 3 | 4 | 3 | 1 | 2 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0004 | 0/0 | 9619 | 12 | 11 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0005 | 1/0 | 9622 | 11 | 8 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0006 | 0/0 | 9621 | 8 | 0 | 5 | 3 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0007 | 0/0 | 9621 | 8 | 8 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0008 | 0/0 | 9621 | 8 | 5 | 3 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0009 | 0/0 | 9621 | 6 | 5 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0010 | 0/0 | 9601 | 5 | 5 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0011 | 0/0 | 9621 | 5 | 1 | 2 | 0 | 2 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0012 | 0/0 | 9621 | 4 | 1 | 1 | 1 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0013 | 0/0 | 9621 | 3 | 0 | 3 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0014 | 0/0 | 9608 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0015 | 0/0 | 9621 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0016 | 0/0 | 9601 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0017 | 0/0 | 9622 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0018 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0019 | 0/0 | 9621 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0020 | 0/0 | 9623 | 2 | 0 | 2 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0021 | 0/0 | 9622 | 2 | 2 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0022 | 0/0 | 9621 | 2 | 0 | 0 | 2 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0023 | 0/0 | 9621 | 2 | 1 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0024 | 0/0 | 9620 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0026 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0027 | 0/0 | 9622 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0028 | 0/0 | 9621 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0029 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0030 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0031 | 0/0 | 9621 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0032 | 0/0 | 9601 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0033 | 0/0 | 9621 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0035 | 0/0 | 9622 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0036 | 0/0 | 9621 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0037 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0038 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0039 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0040 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0041 | 0/0 | 9621 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0043 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0044 | 0/0 | 9622 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0045 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0046 | 0/0 | 9621 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0047 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0048 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0049 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0050 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0051 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0052 | 0/0 | 9600 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0053 | 0/0 | 9619 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0054 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0055 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0056 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0057 | 0/0 | 9621 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0058 | 0/0 | 9621 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0059 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0060 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0061 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0062 | 0/0 | 9622 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0001t0063 | 0/0 | 9621 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0002t0003 | 0/0 | 9621 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0002t0034 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0003t0003 | 0/0 | 9621 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0004t0042 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0006t0025 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0001c0007t0001 | 0/0 | 9621 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| a0002c0005t0018 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | copy fasta | chr11 | 111597449 | 111735855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0011g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0013g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0013g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0014g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0017g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0019g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0019g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0020g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0020g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0021g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0021g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0022g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0023g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0023g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0024g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0026g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0027g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0028g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0029g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0030g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0031g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0032g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0033g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0035g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0036g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0037g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0038g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0039g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0040g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0041g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0043g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0044g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0045g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0046g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0047g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0048g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0049g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0050g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0051g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0052g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0053g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0054g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0055g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0056g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0057g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0058g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0059g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0060g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0061g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0062g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0001t0063g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0002t0034g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0004t0042g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0006t0025g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0001c0007t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| a0002c0005t0018g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | GBR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0193 | EUR | GBR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00140 | hp1 | a0001 | c0001 | t0036 | g0065 | EUR | GBR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0029 | EUR | GBR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00558 | hp1 | a0001 | c0001 | t0063 | g0192 | EAS | CHS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0031 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00642 | hp2 | a0001 | c0002 | t0034 | g0194 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00733 | hp1 | a0001 | c0001 | t0048 | g0071 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0116 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0133 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG00738 | hp2 | a0001 | c0001 | t0050 | g0185 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01069 | hp2 | a0001 | c0001 | t0019 | g0094 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01070 | hp1 | a0001 | c0001 | t0062 | g0018 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01071 | hp2 | a0001 | c0001 | t0019 | g0095 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0117 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01099 | hp2 | a0001 | c0001 | t0020 | g0134 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0177 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01169 | hp1 | a0001 | c0001 | t0027 | g0025 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0184 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0084 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01243 | hp1 | a0001 | c0001 | t0049 | g0145 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0168 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01255 | hp2 | a0001 | c0001 | t0059 | g0004 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0046 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01257 | hp2 | a0001 | c0001 | t0013 | g0188 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01258 | hp1 | a0001 | c0001 | t0023 | g0015 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0039 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0085 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0086 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0032 | EUR | IBS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | IBS | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0081 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0122 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0191 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01943 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0186 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0083 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01978 | hp2 | a0001 | c0001 | t0029 | g0097 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0195 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02055 | hp2 | a0001 | c0001 | t0056 | g0146 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02056 | hp1 | a0001 | c0001 | t0022 | g0050 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02056 | hp2 | a0001 | c0001 | t0031 | g0009 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0170 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0082 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02293 | hp1 | a0001 | c0001 | t0038 | g0028 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0026 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02523 | hp1 | a0001 | c0001 | t0012 | g0035 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02523 | hp2 | a0001 | c0001 | t0041 | g0073 | EAS | KHV | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02572 | hp1 | a0001 | c0001 | t0060 | g0102 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02572 | hp2 | a0001 | c0001 | t0043 | g0160 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0033 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02630 | hp2 | a0001 | c0001 | t0030 | g0121 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02683 | hp2 | a0001 | c0001 | t0028 | g0098 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02717 | hp1 | a0001 | c0001 | t0040 | g0056 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0131 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0128 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0100 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0190 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02895 | hp1 | a0001 | c0001 | t0039 | g0143 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02970 | hp1 | a0001 | c0001 | t0053 | g0118 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02970 | hp2 | a0001 | c0001 | t0032 | g0080 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0076 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02976 | hp2 | a0001 | c0001 | t0054 | g0141 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03041 | hp2 | a0001 | c0001 | t0045 | g0034 | AFR | GWD | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03130 | hp1 | a0002 | c0005 | t0018 | g0101 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0189 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03139 | hp1 | a0001 | c0001 | t0061 | g0103 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0198 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0099 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03453 | hp2 | a0001 | c0001 | t0052 | g0005 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0171 | AFR | ESN | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03579 | hp2 | a0001 | c0001 | t0037 | g0120 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03831 | hp2 | a0001 | c0001 | t0058 | g0010 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03834 | hp2 | a0001 | c0001 | t0057 | g0066 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0175 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18906 | hp2 | a0001 | c0004 | t0042 | g0183 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18939 | hp1 | a0001 | c0001 | t0024 | g0197 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18988 | hp2 | a0001 | c0001 | t0035 | g0060 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18989 | hp1 | a0001 | c0001 | t0033 | g0174 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18994 | hp1 | a0001 | c0001 | t0046 | g0052 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19030 | hp2 | a0001 | c0001 | t0051 | g0153 | AFR | LWK | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0140 | AFR | LWK | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | LWK | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19065 | hp2 | a0001 | c0001 | t0022 | g0008 | EAS | JPT | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0075 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | YRI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | TSI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20752 | hp2 | a0001 | c0001 | t0044 | g0123 | EUR | TSI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20805 | hp1 | a0001 | c0001 | t0011 | g0124 | EUR | TSI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0088 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0137 | AMR | CLM | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02109 | hp2 | a0001 | c0006 | t0025 | g0119 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02486 | hp2 | a0001 | c0001 | t0055 | g0142 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0016 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0164 | AFR | ACB | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG03471 | hp2 | a0001 | c0001 | t0047 | g0001 | AFR | MSL | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0077 | AFR | USA | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | USA | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20300 | hp1 | a0001 | c0001 | t0026 | g0104 | AFR | USA | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | USA | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0014 | REF | REF | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0138 | REF | REF | SIK2_chr11_111597449_111735855 | SIK2 | chr11 | 111597449 | 111735855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111723774
|
G | A | 1 | a0002 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.2426G>A | p.Arg809Gln | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2541/9622 | 2426/2781 | 809/926 | chr11 | 111723774 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111712249
|
G | A | 1 | a0001c0003 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.1140G>A | p.Pro380Pro | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/15 | 1255/9622 | 1140/2781 | 380/926 | chr11 | 111712249 | ||
| chr11:111712282
|
C | T | 1 | a0001c0002 | 2 | HG00099.hp2 HG00642.hp2 |
synonymous_variant | LOW | c.1173C>T | p.Pro391Pro | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/15 | 1288/9622 | 1173/2781 | 391/926 | chr11 | 111712282 | ||
| chr11:111712333
|
G | A | 1 | a0001c0004 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1224G>A | p.Ala408Ala | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/15 | 1339/9622 | 1224/2781 | 408/926 | chr11 | 111712333 | ||
| chr11:111720918
|
A | G | 1 | a0001c0007 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1800A>G | p.Gln600Gln | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/15 | 1915/9622 | 1800/2781 | 600/926 | chr11 | 111720918 | ||
| chr11:111723796
|
G | A | 1 | a0001c0006 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2448G>A | p.Thr816Thr | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2563/9622 | 2448/2781 | 816/926 | chr11 | 111723796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111724344
|
T | C | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 215 | chr11 | 111724344 | |||||
| chr11:111724371
|
C | T | 1 | a0001c0001t0063 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 242 | chr11 | 111724371 | |||||
| chr11:111724442
|
G | C | 48 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(45): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 313 | chr11 | 111724442 | |||||
| chr11:111724465
|
A | G | 3 | a0001c0001t0012a0001c0001t0019a0001c0001t0050 | 7 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*336A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 336 | chr11 | 111724465 | |||||
| chr11:111724538
|
AT | A | 4 | a0001c0001t0004a0001c0001t0051a0001c0001t0052others(1): Show | 15 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*414delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 414 | INFO_REALIGN_3_PRIME | chr11 | 111724538 | ||||
| chr11:111724759
|
G | A | 4 | a0001c0001t0006a0001c0001t0024a0001c0001t0026others(1): Show | 11 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*630G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 630 | chr11 | 111724759 | |||||
| chr11:111725025
|
G | A | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0051others(2): Show | 17 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 896 | chr11 | 111725025 | |||||
| chr11:111725301
|
G | A | 1 | a0001c0001t0027 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1172 | chr11 | 111725301 | |||||
| chr11:111725301
|
G | C | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1172G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1172 | chr11 | 111725301 | |||||
| chr11:111725344
|
A | G | 1 | a0001c0001t0049 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1215A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1215 | chr11 | 111725344 | |||||
| chr11:111725349
|
CAAAG | C | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227_*1230delAGAA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1227 | INFO_REALIGN_3_PRIME | chr11 | 111725349 | ||||
| chr11:111725406
|
A | G | 2 | a0001c0001t0018a0002c0005t0018 | 2 | HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1277A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1277 | chr11 | 111725406 | |||||
| chr11:111725420
|
T | G | 1 | a0001c0001t0028 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1291 | chr11 | 111725420 | |||||
| chr11:111725986
|
AGTT | A | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1861_*1863delGTT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 1861 | INFO_REALIGN_3_PRIME | chr11 | 111725986 | ||||
| chr11:111726452
|
G | A | 1 | a0001c0001t0029 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2323G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2323 | chr11 | 111726452 | |||||
| chr11:111726517
|
GCTTAT | G | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2392_*2396delATCT others(1): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2392 | INFO_REALIGN_3_PRIME | chr11 | 111726517 | ||||
| chr11:111726577
|
A | G | 1 | a0001c0001t0048 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2448A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2448 | chr11 | 111726577 | |||||
| chr11:111726718
|
A | G | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2589A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2589 | chr11 | 111726718 | |||||
| chr11:111726742
|
G | A | 1 | a0001c0001t0031 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2613G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 2613 | chr11 | 111726742 | |||||
| chr11:111727177
|
C | T | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3048C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3048 | chr11 | 111727177 | |||||
| chr11:111727230
|
C | G | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3101C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3101 | chr11 | 111727230 | |||||
| chr11:111727286
|
A | G | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3157A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3157 | chr11 | 111727286 | |||||
| chr11:111727349
|
C | A | 2 | a0001c0001t0018a0002c0005t0018 | 2 | HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3220C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3220 | chr11 | 111727349 | |||||
| chr11:111727584
|
A | G | 2 | a0001c0001t0014a0001c0001t0023 | 4 | HG00733.hp2 HG01099.hp1 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3455A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3455 | chr11 | 111727584 | |||||
| chr11:111727601
|
A | G | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3472A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3472 | chr11 | 111727601 | |||||
| chr11:111727743
|
G | A | 1 | a0001c0001t0051 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3614G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3614 | chr11 | 111727743 | |||||
| chr11:111727744
|
T | A | 1 | a0001c0001t0051 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3615T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3615 | chr11 | 111727744 | |||||
| chr11:111727813
|
G | A | 3 | a0001c0001t0010a0001c0001t0016a0001c0001t0032 | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3684G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3684 | chr11 | 111727813 | |||||
| chr11:111727862
|
C | G | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3733C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3733 | chr11 | 111727862 | |||||
| chr11:111727876
|
C | T | 1 | a0001c0001t0016 | 2 | HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3747C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3747 | chr11 | 111727876 | |||||
| chr11:111727954
|
A | G | 1 | a0001c0001t0026 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3825A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3825 | chr11 | 111727954 | |||||
| chr11:111727979
|
A | G | 1 | a0001c0001t0046 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3850A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3850 | chr11 | 111727979 | |||||
| chr11:111728120
|
A | G | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3991A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 3991 | chr11 | 111728120 | |||||
| chr11:111728237
|
A | C | 1 | a0001c0001t0021 | 2 | HG02717.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4108A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4108 | chr11 | 111728237 | |||||
| chr11:111728292
|
AT | A | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*4177delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4177 | INFO_REALIGN_3_PRIME | chr11 | 111728292 | ||||
| chr11:111728369
|
A | T | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4240A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4240 | chr11 | 111728369 | |||||
| chr11:111728568
|
T | C | 10 | a0001c0001t0007a0001c0001t0010a0001c0001t0014others(7): Show | 23 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4439T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4439 | chr11 | 111728568 | |||||
| chr11:111728619
|
G | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4490G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4490 | chr11 | 111728619 | |||||
| chr11:111728620
|
C | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4491C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4491 | chr11 | 111728620 | |||||
| chr11:111728622
|
A | G | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4493A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4493 | chr11 | 111728622 | |||||
| chr11:111728628
|
G | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4499G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4499 | chr11 | 111728628 | |||||
| chr11:111728632
|
G | C | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4503G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4503 | chr11 | 111728632 | |||||
| chr11:111728634
|
C | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4505C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4505 | chr11 | 111728634 | |||||
| chr11:111728636
|
A | C | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4507A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4507 | chr11 | 111728636 | |||||
| chr11:111728637
|
G | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4508G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4508 | chr11 | 111728637 | |||||
| chr11:111728638
|
A | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4509A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4509 | chr11 | 111728638 | |||||
| chr11:111728639
|
G | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4510G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4510 | chr11 | 111728639 | |||||
| chr11:111728656
|
C | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4527C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4527 | chr11 | 111728656 | |||||
| chr11:111728667
|
G | A | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4538G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4538 | chr11 | 111728667 | |||||
| chr11:111728680
|
A | G | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4551A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4551 | chr11 | 111728680 | |||||
| chr11:111728681
|
C | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4552C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4552 | chr11 | 111728681 | |||||
| chr11:111728700
|
A | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4571A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4571 | chr11 | 111728700 | |||||
| chr11:111728703
|
C | T | 2 | a0001c0001t0043a0001c0004t0042 | 2 | HG02572.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4574C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4574 | chr11 | 111728703 | |||||
| chr11:111728710
|
C | T | 3 | a0001c0001t0047a0001c0001t0060a0001c0001t0061 | 3 | HG02572.hp1 HG03139.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4581C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4581 | chr11 | 111728710 | |||||
| chr11:111728740
|
C | A | 1 | a0001c0001t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4611C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4611 | chr11 | 111728740 | |||||
| chr11:111728741
|
A | G | 1 | a0001c0001t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4612A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4612 | chr11 | 111728741 | |||||
| chr11:111728749
|
G | C | 1 | a0001c0001t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4620G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4620 | chr11 | 111728749 | |||||
| chr11:111728781
|
G | A | 2 | a0001c0001t0018a0002c0005t0018 | 2 | HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4652G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4652 | chr11 | 111728781 | |||||
| chr11:111728787
|
G | A | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0013others(8): Show | 30 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4658G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4658 | chr11 | 111728787 | |||||
| chr11:111728792
|
T | C | 18 | a0001c0001t0003a0001c0001t0006a0001c0001t0009others(15): Show | 44 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4663T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4663 | chr11 | 111728792 | |||||
| chr11:111728797
|
G | T | 1 | a0001c0001t0007 | 8 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4668G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4668 | chr11 | 111728797 | |||||
| chr11:111728803
|
A | G | 1 | a0001c0001t0007 | 8 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4674A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4674 | chr11 | 111728803 | |||||
| chr11:111728806
|
T | C | 5 | a0001c0001t0007a0001c0001t0013a0001c0001t0028others(2): Show | 14 | HG01070.hp1 HG01169.hp2 HG01257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4677T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4677 | chr11 | 111728806 | |||||
| chr11:111728840
|
C | T | 1 | a0001c0001t0061 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4711C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4711 | chr11 | 111728840 | |||||
| chr11:111728855
|
T | C | 24 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(21): Show | 59 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4726T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4726 | chr11 | 111728855 | |||||
| chr11:111728856
|
G | A | 1 | a0001c0001t0019 | 2 | HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4727G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4727 | chr11 | 111728856 | |||||
| chr11:111728873
|
A | G | 4 | a0001c0001t0010a0001c0001t0016a0001c0001t0032others(1): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4744A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4744 | chr11 | 111728873 | |||||
| chr11:111728906
|
A | T | 4 | a0001c0001t0013a0001c0001t0014a0001c0001t0028others(1): Show | 7 | HG00733.hp2 HG01099.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4777A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4777 | chr11 | 111728906 | |||||
| chr11:111728911
|
A | C | 1 | a0001c0001t0040 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4782A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4782 | chr11 | 111728911 | |||||
| chr11:111728911
|
A | G | 3 | a0001c0001t0041a0001c0001t0048a0001c0002t0034 | 3 | HG00642.hp2 HG00733.hp1 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4782A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4782 | chr11 | 111728911 | |||||
| chr11:111728919
|
A | G | 3 | a0001c0001t0004a0001c0001t0039a0001c0001t0051 | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4790A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4790 | chr11 | 111728919 | |||||
| chr11:111728920
|
C | T | 3 | a0001c0001t0004a0001c0001t0039a0001c0001t0051 | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4791C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4791 | chr11 | 111728920 | |||||
| chr11:111728923
|
C | CA | 3 | a0001c0001t0017a0001c0001t0020a0001c0001t0035 | 5 | HG00738.hp1 HG01099.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4809dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4810 | INFO_REALIGN_3_PRIME | chr11 | 111728923 | ||||
| chr11:111728923
|
CA | C | 9 | a0001c0001t0004a0001c0001t0014a0001c0001t0018others(6): Show | 21 | HG00733.hp2 HG01099.hp1 HG01952.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4809delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4809 | INFO_REALIGN_3_PRIME | chr11 | 111728923 | ||||
| chr11:111728938
|
A | G | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(9): Show | 30 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4809A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4809 | chr11 | 111728938 | |||||
| chr11:111729095
|
A | G | 3 | a0001c0001t0039a0001c0001t0047a0001c0006t0025 | 3 | HG02109.hp2 HG02895.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4966A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 4966 | chr11 | 111729095 | |||||
| chr11:111729142
|
A | G | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5013A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5013 | chr11 | 111729142 | |||||
| chr11:111729230
|
C | T | 1 | a0001c0001t0033 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5101C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5101 | chr11 | 111729230 | |||||
| chr11:111729710
|
T | C | 1 | a0001c0001t0036 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5581T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5581 | chr11 | 111729710 | |||||
| chr11:111729765
|
G | A | 1 | a0001c0001t0038 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5636G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5636 | chr11 | 111729765 | |||||
| chr11:111729801
|
C | T | 1 | a0001c0001t0059 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5672C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5672 | chr11 | 111729801 | |||||
| chr11:111729947
|
T | C | 2 | a0001c0001t0014a0001c0001t0047 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5818T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5818 | chr11 | 111729947 | |||||
| chr11:111729965
|
G | C | 2 | a0001c0001t0014a0001c0001t0047 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5836G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5836 | chr11 | 111729965 | |||||
| chr11:111729972
|
C | T | 2 | a0001c0001t0014a0001c0001t0047 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5843C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5843 | chr11 | 111729972 | |||||
| chr11:111729976
|
CGGCATCA others(13): Show |
C | 4 | a0001c0001t0010a0001c0001t0016a0001c0001t0032others(1): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5851_*5870delATCA others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5851 | INFO_REALIGN_3_PRIME | chr11 | 111729976 | ||||
| chr11:111729977
|
G | A | 1 | a0001c0001t0022 | 2 | HG02056.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5848G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 5848 | chr11 | 111729977 | |||||
| chr11:111730458
|
A | G | 1 | a0001c0001t0053 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6329A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 6329 | chr11 | 111730458 | |||||
| chr11:111730571
|
C | T | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*6442C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 15/15 | 6442 | chr11 | 111730571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111602901
|
C | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.135+203C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111602901 | ||||||
| chr11:111603010
|
C | A | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135+312C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603010 | ||||||
| chr11:111603053
|
C | T | 1 | a0001c0001t0024g0197 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135+355C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603053 | ||||||
| chr11:111603307
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | NA18968.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.135+609G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603307 | ||||||
| chr11:111603392
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+694G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603392 | ||||||
| chr11:111603492
|
T | TACTCATA others(44): Show |
1 | a0001c0001t0028g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.135+795_135+845dup others(51): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111603492 | |||||
| chr11:111603607
|
C | A | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.135+909C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603607 | ||||||
| chr11:111603716
|
CT | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.135+1019delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603716 | ||||||
| chr11:111603723
|
T | C | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.135+1025T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603723 | ||||||
| chr11:111603845
|
G | A | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.135+1147G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111603845 | ||||||
| chr11:111604268
|
G | C | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+1570G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111604268 | ||||||
| chr11:111604616
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+1918A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111604616 | ||||||
| chr11:111604757
|
A | G | 1 | a0001c0001t0029g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.135+2059A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111604757 | ||||||
| chr11:111604957
|
A | AT | 57 | a0001c0001t0002g0180a0001c0001t0002g0196a0001c0001t0003g0159others(54): Show | 57 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.135+2277dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111604957 | |||||
| chr11:111604957
|
AT | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.135+2277delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111604957 | |||||
| chr11:111605036
|
C | T | 9 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+2338C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605036 | ||||||
| chr11:111605051
|
C | T | 2 | a0001c0001t0006g0089a0001c0001t0006g0090 | 2 | NA18965.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.135+2353C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605051 | ||||||
| chr11:111605190
|
T | G | 1 | a0001c0001t0059g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.135+2492T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605190 | ||||||
| chr11:111605271
|
T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+2573T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605271 | ||||||
| chr11:111605327
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+2629G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605327 | ||||||
| chr11:111605402
|
A | G | 1 | a0001c0001t0005g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+2704A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605402 | ||||||
| chr11:111605407
|
A | T | 1 | a0001c0001t0061g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+2709A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605407 | ||||||
| chr11:111605521
|
A | G | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135+2823A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605521 | ||||||
| chr11:111605546
|
T | C | 1 | a0001c0001t0049g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135+2848T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605546 | ||||||
| chr11:111605593
|
T | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.135+2895T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605593 | ||||||
| chr11:111605910
|
G | T | 9 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+3212G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605910 | ||||||
| chr11:111605931
|
C | A | 1 | a0001c0001t0002g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.135+3233C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111605931 | ||||||
| chr11:111606257
|
G | A | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+3559G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606257 | ||||||
| chr11:111606394
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.135+3696G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606394 | ||||||
| chr11:111606438
|
G | A | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+3740G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606438 | ||||||
| chr11:111606484
|
T | G | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.135+3786T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606484 | ||||||
| chr11:111606601
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.135+3903A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606601 | ||||||
| chr11:111606609
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+3911C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606609 | ||||||
| chr11:111606641
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.135+3943C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606641 | ||||||
| chr11:111606663
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+3965A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606663 | ||||||
| chr11:111606759
|
A | G | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.135+4061A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606759 | ||||||
| chr11:111606956
|
G | GAA | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.135+4270_135+4271d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111606956 | |||||
| chr11:111606972
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.135+4274T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606972 | ||||||
| chr11:111606974
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.135+4276T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111606974 | ||||||
| chr11:111607260
|
T | C | 8 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+4562T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607260 | ||||||
| chr11:111607504
|
A | G | 1 | a0001c0001t0039g0143 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.135+4806A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607504 | ||||||
| chr11:111607546
|
A | G | 15 | a0001c0001t0002g0196a0001c0001t0004g0107a0001c0001t0004g0147others(12): Show | 15 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+4848A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607546 | ||||||
| chr11:111607685
|
A | C | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+4987A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607685 | ||||||
| chr11:111607899
|
A | G | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.135+5201A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607899 | ||||||
| chr11:111607996
|
A | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0037others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.135+5298A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111607996 | ||||||
| chr11:111608013
|
G | C | 1 | a0001c0001t0007g0108 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.135+5315G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111608013 | ||||||
| chr11:111608170
|
C | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+5472C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111608170 | ||||||
| chr11:111608562
|
T | C | 1 | a0001c0001t0043g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.135+5864T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111608562 | ||||||
| chr11:111608788
|
A | C | 2 | a0001c0001t0002g0196a0001c0001t0007g0115 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.135+6090A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111608788 | ||||||
| chr11:111608989
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.135+6291T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111608989 | ||||||
| chr11:111608999
|
A | AT | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+6308dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111608999 | |||||
| chr11:111609098
|
T | C | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.135+6400T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609098 | ||||||
| chr11:111609102
|
T | TTGCATTC others(310): Show |
6 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+6416_135+6417i others(319): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111609102 | |||||
| chr11:111609102
|
T | TTGCATTC others(311): Show |
2 | a0001c0001t0010g0081a0001c0001t0032g0080 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.135+6416_135+6417i others(320): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111609102 | |||||
| chr11:111609102
|
T | TTGCATTC others(322): Show |
1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.135+6416_135+6417i others(331): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111609102 | |||||
| chr11:111609119
|
A | G | 2 | a0001c0001t0054g0141a0001c0001t0055g0142 | 2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.135+6421A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609119 | ||||||
| chr11:111609138
|
C | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135+6440C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609138 | ||||||
| chr11:111609218
|
C | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.135+6520C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609218 | ||||||
| chr11:111609263
|
G | A | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+6565G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609263 | ||||||
| chr11:111609308
|
A | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135+6610A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609308 | ||||||
| chr11:111609335
|
G | C | 3 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG01069.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.135+6637G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609335 | ||||||
| chr11:111609392
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+6694C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609392 | ||||||
| chr11:111609549
|
T | C | 5 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(2): Show | 5 | HG01952.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-6694T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609549 | ||||||
| chr11:111609776
|
T | C | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-6467T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609776 | ||||||
| chr11:111609786
|
T | G | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-6457T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609786 | ||||||
| chr11:111609789
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.136-6454A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111609789 | ||||||
| chr11:111610328
|
A | G | 1 | a0001c0003t0003g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.136-5915A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610328 | ||||||
| chr11:111610423
|
A | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136-5820A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610423 | ||||||
| chr11:111610465
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.136-5778G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610465 | ||||||
| chr11:111610477
|
G | A | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-5766G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610477 | ||||||
| chr11:111610479
|
C | G | 1 | a0001c0001t0005g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.136-5764C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610479 | ||||||
| chr11:111610591
|
GTCC | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-5647_136-5645d others(5): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111610591 | |||||
| chr11:111610894
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136-5349T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610894 | ||||||
| chr11:111610981
|
C | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136-5262C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111610981 | ||||||
| chr11:111611030
|
G | A | 1 | a0001c0001t0004g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136-5213G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611030 | ||||||
| chr11:111611085
|
AAT | A | 16 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-5157_136-5156d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611085 | ||||||
| chr11:111611085
|
AATGT | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(66): Show | 69 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.136-5157_136-5154d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611085 | ||||||
| chr11:111611086
|
A | ATG | 64 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0180others(61): Show | 64 | HG00738.hp2 HG01109.hp2 HG01169.hp2 others(61): Show |
intron_variant | MODIFIER | c.136-5126_136-5125d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111611086 | |||||
| chr11:111611086
|
A | ATGTG | 16 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163others(13): Show | 16 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.136-5128_136-5125d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111611086 | |||||
| chr11:111611086
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0041g0073a0001c0001t0048g0071 | 3 | HG00733.hp1 HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.136-5157A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611086 | ||||||
| chr11:111611086
|
ATG | A | 11 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-5126_136-5125d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111611086 | |||||
| chr11:111611210
|
G | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.136-5033G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611210 | ||||||
| chr11:111611248
|
CA | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.136-4981delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111611248 | |||||
| chr11:111611301
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.136-4942T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611301 | ||||||
| chr11:111611521
|
C | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-4722C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111611521 | ||||||
| chr11:111612165
|
C | T | 1 | a0001c0001t0006g0088 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.136-4078C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612165 | ||||||
| chr11:111612278
|
C | T | 1 | a0001c0001t0013g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.136-3965C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612278 | ||||||
| chr11:111612461
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.136-3782G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612461 | ||||||
| chr11:111612582
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-3661A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612582 | ||||||
| chr11:111612915
|
G | GAT | 2 | a0001c0001t0003g0125a0001c0001t0008g0190 | 2 | HG01516.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.136-3297_136-3296d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATAT | 2 | a0001c0001t0007g0115a0001c0001t0021g0128 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.136-3299_136-3296d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATAT | 7 | a0001c0001t0007g0109a0001c0001t0007g0112a0001c0001t0007g0113others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-3301_136-3296d others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(1): Show |
7 | a0001c0001t0001g0106a0001c0001t0005g0126a0001c0001t0005g0127others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-3303_136-3296d others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(3): Show |
14 | a0001c0001t0001g0105a0001c0001t0003g0187a0001c0001t0004g0107others(11): Show | 14 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-3305_136-3296d others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(5): Show |
12 | a0001c0001t0002g0180a0001c0001t0003g0181a0001c0001t0003g0182others(9): Show | 12 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-3307_136-3296d others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(7): Show |
12 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0004g0150others(9): Show | 12 | HG01109.hp2 HG02647.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-3309_136-3296d others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(9): Show |
7 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0008g0169others(4): Show | 7 | HG01255.hp1 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-3311_136-3296d others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(11): Show |
5 | a0001c0001t0003g0159a0001c0001t0003g0167a0001c0001t0028g0098others(2): Show | 5 | HG00558.hp1 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-3313_136-3296d others(20): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(13): Show |
7 | a0001c0001t0003g0165a0001c0001t0004g0148a0001c0001t0004g0149others(4): Show | 7 | HG01891.hp2 HG01952.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-3315_136-3296d others(22): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(15): Show |
1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-3317_136-3296d others(24): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
G | GATATATA others(17): Show |
1 | a0001c0001t0004g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-3319_136-3296d others(26): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
GATATATA others(1): Show |
G | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136-3303_136-3296d others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
GATATATA others(5): Show |
G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-3307_136-3296d others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612915
|
GATATATA others(9): Show |
G | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.136-3311_136-3296d others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612915 | |||||
| chr11:111612931
|
T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-3312T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612931 | ||||||
| chr11:111612938
|
A | ATATATAT others(11): Show |
1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.136-3296_136-3295i others(20): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612938 | |||||
| chr11:111612938
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0018g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-3296_136-3295i others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612938 | |||||
| chr11:111612944
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG01069.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.136-3296_136-3295i others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111612944 | |||||
| chr11:111612948
|
T | A | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-3295T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111612948 | ||||||
| chr11:111613140
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.136-3103A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613140 | ||||||
| chr11:111613310
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.136-2933C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613310 | ||||||
| chr11:111613326
|
A | G | 2 | a0001c0001t0010g0079a0001c0001t0010g0081 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.136-2917A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613326 | ||||||
| chr11:111613389
|
A | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-2854A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613389 | ||||||
| chr11:111613489
|
A | G | 1 | a0001c0001t0014g0117 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.136-2754A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613489 | ||||||
| chr11:111613887
|
C | T | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.136-2356C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613887 | ||||||
| chr11:111613995
|
A | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-2248A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111613995 | ||||||
| chr11:111614039
|
C | G | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.136-2204C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614039 | ||||||
| chr11:111614045
|
C | T | 1 | a0001c0001t0008g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.136-2198C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614045 | ||||||
| chr11:111614085
|
A | AT | 93 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0019others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.136-2142dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111614085 | |||||
| chr11:111614085
|
A | ATT | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0072others(2): Show | 5 | HG00733.hp1 HG02523.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-2143_136-2142d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111614085 | |||||
| chr11:111614210
|
T | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-2033T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614210 | ||||||
| chr11:111614306
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.136-1937A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614306 | ||||||
| chr11:111614363
|
C | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-1880C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614363 | ||||||
| chr11:111614476
|
A | T | 2 | a0001c0001t0019g0094a0001c0001t0019g0095 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.136-1767A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614476 | ||||||
| chr11:111614610
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.136-1633T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614610 | ||||||
| chr11:111614913
|
C | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.136-1330C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111614913 | ||||||
| chr11:111615011
|
C | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG00621.hp1 NA18939.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-1232C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615011 | ||||||
| chr11:111615138
|
CA | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.136-1102delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111615138 | |||||
| chr11:111615250
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.136-993A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615250 | ||||||
| chr11:111615288
|
T | TA | 115 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(112): Show | 115 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.136-939dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111615288 | |||||
| chr11:111615288
|
TA | T | 5 | a0001c0001t0011g0026a0001c0001t0011g0027a0001c0001t0011g0029others(2): Show | 5 | HG00140.hp2 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-939delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 111615288 | |||||
| chr11:111615319
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.136-924C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615319 | ||||||
| chr11:111615401
|
T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-842T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615401 | ||||||
| chr11:111615412
|
T | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-831T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615412 | ||||||
| chr11:111615832
|
C | T | 1 | a0001c0001t0009g0166 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-411C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615832 | ||||||
| chr11:111615883
|
G | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.136-360G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111615883 | ||||||
| chr11:111616004
|
A | T | 1 | a0001c0001t0010g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-239A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111616004 | ||||||
| chr11:111616014
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.136-229A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111616014 | ||||||
| chr11:111616026
|
A | G | 1 | a0001c0001t0015g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.136-217A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 1/14 | chr11 | 111616026 | ||||||
| chr11:111616382
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.252+23C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111616382 | ||||||
| chr11:111616710
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.252+351G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111616710 | ||||||
| chr11:111616835
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.252+476A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111616835 | ||||||
| chr11:111616871
|
T | C | 15 | a0001c0001t0002g0196a0001c0001t0004g0107a0001c0001t0004g0147others(12): Show | 15 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+512T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111616871 | ||||||
| chr11:111617166
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.252+807A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617166 | ||||||
| chr11:111617190
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.252+831A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617190 | ||||||
| chr11:111617214
|
T | C | 2 | a0001c0001t0008g0178a0001c0001t0017g0171 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.252+855T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617214 | ||||||
| chr11:111617226
|
C | G | 4 | a0001c0001t0011g0026a0001c0001t0011g0027a0001c0001t0011g0029others(1): Show | 4 | HG00140.hp2 HG01943.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+867C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617226 | ||||||
| chr11:111617407
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.252+1048T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617407 | ||||||
| chr11:111617808
|
C | CAT | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.252+1449_252+1450i others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617808 | ||||||
| chr11:111617826
|
G | A | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.252+1467G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617826 | ||||||
| chr11:111617828
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.252+1469G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617828 | ||||||
| chr11:111617850
|
G | GTA | 2 | a0001c0001t0010g0081a0001c0001t0037g0120 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.252+1502_252+1503d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 111617850 | |||||
| chr11:111617859
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+1500T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617859 | ||||||
| chr11:111617859
|
T | TAC | 26 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(23): Show | 26 | HG01070.hp1 HG01255.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.252+1501_252+1502i others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 111617859 | |||||
| chr11:111617861
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.252+1502T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111617861 | ||||||
| chr11:111618004
|
G | A | 2 | a0001c0001t0022g0008a0001c0001t0031g0009 | 2 | HG02056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.252+1645G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111618004 | ||||||
| chr11:111618344
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.252+1985G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111618344 | ||||||
| chr11:111618391
|
A | G | 3 | a0001c0001t0047g0001a0001c0006t0025g0119a0001c0007t0001g0198 | 3 | HG02109.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.253-1948A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111618391 | ||||||
| chr11:111618685
|
T | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.253-1654T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111618685 | ||||||
| chr11:111618898
|
TC | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.253-1440delC | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111618898 | ||||||
| chr11:111619244
|
G | A | 1 | a0001c0001t0013g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.253-1095G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619244 | ||||||
| chr11:111619323
|
T | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.253-1016T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619323 | ||||||
| chr11:111619543
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0002g0091 | 2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.253-796C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619543 | ||||||
| chr11:111619602
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.253-737C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619602 | ||||||
| chr11:111619696
|
G | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.253-643G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619696 | ||||||
| chr11:111619713
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.253-626T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619713 | ||||||
| chr11:111619817
|
TATAGTAC others(4): Show |
T | 1 | a0001c0001t0027g0025 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.253-520_253-510del others(11): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 111619817 | |||||
| chr11:111619828
|
G | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-511G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619828 | ||||||
| chr11:111619961
|
A | T | 1 | a0001c0001t0013g0188 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.253-378A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 2/14 | chr11 | 111619961 | ||||||
| chr11:111620598
|
A | G | 45 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(42): Show | 45 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.316+196A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111620598 | ||||||
| chr11:111620907
|
A | C | 1 | a0001c0001t0017g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.316+505A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111620907 | ||||||
| chr11:111621100
|
T | A | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+698T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621100 | ||||||
| chr11:111621164
|
G | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+762G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621164 | ||||||
| chr11:111621209
|
C | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+807C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621209 | ||||||
| chr11:111621495
|
ATC | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.316+1095_316+1096d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111621495 | |||||
| chr11:111621627
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+1225A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621627 | ||||||
| chr11:111621688
|
G | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+1286G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621688 | ||||||
| chr11:111621839
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+1437G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621839 | ||||||
| chr11:111621867
|
C | T | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.316+1465C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621867 | ||||||
| chr11:111621892
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+1490A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111621892 | ||||||
| chr11:111622014
|
T | C | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+1612T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622014 | ||||||
| chr11:111622137
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+1735T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622137 | ||||||
| chr11:111622247
|
CT | C | 74 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0180others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.316+1871delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111622247 | |||||
| chr11:111622247
|
CTT | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0002g0074others(5): Show | 8 | HG01099.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+1870_316+1871d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111622247 | |||||
| chr11:111622247
|
CTTT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.316+1869_316+1871d others(5): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111622247 | |||||
| chr11:111622349
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+1947A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622349 | ||||||
| chr11:111622356
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316+1954C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622356 | ||||||
| chr11:111622452
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.316+2050C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622452 | ||||||
| chr11:111622487
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.316+2085A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622487 | ||||||
| chr11:111622501
|
G | A | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+2099G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622501 | ||||||
| chr11:111622543
|
C | T | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+2141C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622543 | ||||||
| chr11:111622544
|
G | A | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316+2142G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622544 | ||||||
| chr11:111622660
|
A | T | 1 | a0001c0001t0040g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.316+2258A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622660 | ||||||
| chr11:111622704
|
T | C | 1 | a0001c0001t0048g0071 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.316+2302T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622704 | ||||||
| chr11:111622714
|
TTAAA | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+2315_316+2318d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111622714 | |||||
| chr11:111622866
|
A | G | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.316+2464A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111622866 | ||||||
| chr11:111623016
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0055others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+2614C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623016 | ||||||
| chr11:111623178
|
C | T | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.316+2776C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623178 | ||||||
| chr11:111623186
|
T | G | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+2784T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623186 | ||||||
| chr11:111623227
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+2825A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623227 | ||||||
| chr11:111623239
|
C | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+2837C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623239 | ||||||
| chr11:111623615
|
T | C | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.316+3213T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623615 | ||||||
| chr11:111623636
|
G | A | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+3234G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623636 | ||||||
| chr11:111623855
|
G | A | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+3453G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111623855 | ||||||
| chr11:111624031
|
A | C | 1 | a0001c0001t0001g0003 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.316+3629A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111624031 | ||||||
| chr11:111624223
|
A | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.316+3821A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111624223 | ||||||
| chr11:111624454
|
A | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.316+4052A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111624454 | ||||||
| chr11:111624464
|
T | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+4062T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111624464 | ||||||
| chr11:111624641
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.316+4239G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111624641 | ||||||
| chr11:111624753
|
A | AAGGCTGG others(49): Show |
1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+4389_316+4444d others(58): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111624753 | |||||
| chr11:111624753
|
AAGGCTGG others(49): Show |
A | 2 | a0001c0001t0005g0135a0001c0001t0012g0035 | 2 | HG02523.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.316+4389_316+4444d others(58): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111624753 | |||||
| chr11:111625055
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+4653G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625055 | ||||||
| chr11:111625174
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.316+4772C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625174 | ||||||
| chr11:111625528
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.316+5126G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625528 | ||||||
| chr11:111625580
|
A | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+5178A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625580 | ||||||
| chr11:111625634
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+5232A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625634 | ||||||
| chr11:111625935
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.316+5533G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111625935 | ||||||
| chr11:111626137
|
G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.316+5735G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626137 | ||||||
| chr11:111626198
|
T | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316+5796T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626198 | ||||||
| chr11:111626227
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316+5825A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626227 | ||||||
| chr11:111626459
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+6057T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626459 | ||||||
| chr11:111626467
|
A | G | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.316+6065A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626467 | ||||||
| chr11:111626576
|
C | T | 1 | a0001c0001t0014g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.316+6174C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626576 | ||||||
| chr11:111626668
|
TTTTA | T | 3 | a0001c0001t0013g0188a0001c0001t0013g0191a0001c0001t0028g0098 | 3 | HG01257.hp2 HG01934.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.316+6274_316+6277d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111626668 | |||||
| chr11:111626680
|
T | G | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+6278T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626680 | ||||||
| chr11:111626710
|
C | CA | 80 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0002g0180others(77): Show | 80 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.316+6320dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111626710 | |||||
| chr11:111626710
|
C | CAA | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.316+6319_316+6320d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111626710 | |||||
| chr11:111626815
|
A | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+6413A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111626815 | ||||||
| chr11:111627089
|
G | T | 1 | a0001c0001t0041g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.316+6687G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627089 | ||||||
| chr11:111627105
|
T | C | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+6703T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627105 | ||||||
| chr11:111627155
|
C | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+6753C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627155 | ||||||
| chr11:111627178
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+6776G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627178 | ||||||
| chr11:111627270
|
A | T | 1 | a0001c0001t0006g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.316+6868A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627270 | ||||||
| chr11:111627799
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.316+7397G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627799 | ||||||
| chr11:111627926
|
G | A | 1 | a0001c0001t0036g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.316+7524G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111627926 | ||||||
| chr11:111628083
|
T | TCCTCAGT others(25): Show |
1 | a0001c0001t0002g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.316+7682_316+7713d others(34): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628083 | |||||
| chr11:111628097
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+7695A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628097 | ||||||
| chr11:111628141
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.316+7739C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628141 | ||||||
| chr11:111628225
|
C | T | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+7823C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628225 | ||||||
| chr11:111628416
|
A | ATCTATCT others(213): Show |
1 | a0001c0001t0002g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.316+8017_316+8018i others(222): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTCTT others(32): Show |
1 | a0001c0001t0002g0091 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.316+8018_316+8019i others(41): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(49): Show |
1 | a0001c0001t0057g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.316+8032_316+8033i others(58): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(13): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0010g0079others(2): Show | 5 | HG00140.hp1 HG02486.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+8032_316+8051d others(22): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(17): Show |
23 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0051others(20): Show | 23 | HG00621.hp1 HG00621.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.316+8028_316+8051d others(26): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(21): Show |
13 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0049others(10): Show | 13 | HG00099.hp1 HG01123.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.316+8024_316+8051d others(30): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(25): Show |
9 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0008g0039others(6): Show | 9 | HG00140.hp2 HG01070.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+8020_316+8051d others(34): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(29): Show |
11 | a0001c0001t0001g0070a0001c0001t0001g0096a0001c0001t0006g0086others(8): Show | 11 | HG00733.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+8016_316+8051d others(38): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(33): Show |
7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG00558.hp2 HG00738.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+8051_316+8052i others(42): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(37): Show |
2 | a0001c0001t0002g0006a0001c0001t0012g0031 | 2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(46): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(41): Show |
3 | a0001c0001t0001g0093a0001c0001t0002g0014a0001c0001t0023g0015 | 3 | HG01109.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(50): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(45): Show |
1 | a0001c0001t0001g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(54): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(49): Show |
2 | a0001c0001t0019g0094a0001c0001t0019g0095 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(58): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(53): Show |
2 | a0001c0001t0001g0013a0001c0001t0002g0020 | 2 | HG01261.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(62): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(57): Show |
5 | a0001c0001t0001g0092a0001c0001t0002g0011a0001c0001t0002g0012others(2): Show | 5 | HG01255.hp2 HG01975.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+8051_316+8052i others(66): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(81): Show |
1 | a0001c0001t0031g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(90): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(101): Show |
1 | a0001c0001t0022g0008 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(110): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
A | ATCTTTCT others(173): Show |
1 | a0001c0001t0058g0010 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(182): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
ATCTT | A | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0037g0120 | 3 | HG02886.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.316+8048_316+8051d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
ATCTTTCT others(1): Show |
A | 39 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0196others(36): Show | 39 | HG00733.hp2 HG01099.hp1 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.316+8044_316+8051d others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
ATCTTTCT others(5): Show |
A | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.316+8040_316+8051d others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628416
|
ATCTTTCT others(9): Show |
A | 1 | a0001c0001t0018g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316+8036_316+8051d others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628416 | |||||
| chr11:111628435
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.316+8033T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628435 | ||||||
| chr11:111628451
|
T | TTTCTTTC others(13): Show |
2 | a0001c0001t0016g0075a0001c0001t0016g0076 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(22): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628451 | |||||
| chr11:111628451
|
T | TTTCTTTC others(24): Show |
2 | a0001c0001t0001g0036a0001c0001t0002g0017 | 2 | NA18979.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.316+8051_316+8052i others(33): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628451 | |||||
| chr11:111628452
|
T | TTCTTTCT others(51): Show |
1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.316+8051_316+8052i others(60): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111628452 | |||||
| chr11:111628453
|
T | TCTTTCTT others(18): Show |
1 | a0001c0001t0002g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.316+8051_316+8052i others(27): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628453 | ||||||
| chr11:111628453
|
T | TCTTTCTT others(22): Show |
1 | a0001c0001t0001g0045 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(31): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628453 | ||||||
| chr11:111628453
|
T | TCTTTCTT others(30): Show |
1 | a0001c0001t0002g0063 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.316+8051_316+8052i others(39): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628453 | ||||||
| chr11:111628454
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.316+8052T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628454 | ||||||
| chr11:111628788
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+8386G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628788 | ||||||
| chr11:111628860
|
C | T | 3 | a0001c0001t0008g0169a0001c0001t0008g0178a0001c0001t0017g0171 | 3 | HG02647.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.316+8458C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628860 | ||||||
| chr11:111628988
|
T | C | 2 | a0001c0001t0008g0039a0001c0001t0008g0046 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.316+8586T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628988 | ||||||
| chr11:111628994
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+8592T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111628994 | ||||||
| chr11:111629209
|
C | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.316+8807C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111629209 | ||||||
| chr11:111629302
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+8900T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111629302 | ||||||
| chr11:111629721
|
C | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+9319C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111629721 | ||||||
| chr11:111629944
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.316+9542C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111629944 | ||||||
| chr11:111630036
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+9634C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630036 | ||||||
| chr11:111630120
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+9718A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630120 | ||||||
| chr11:111630181
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+9779A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630181 | ||||||
| chr11:111630193
|
T | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+9791T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630193 | ||||||
| chr11:111630355
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+9953C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630355 | ||||||
| chr11:111630497
|
CA | C | 15 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(12): Show | 15 | HG01255.hp2 HG01952.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.316+10105delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111630497 | |||||
| chr11:111630542
|
T | C | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.316+10140T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630542 | ||||||
| chr11:111630714
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+10312G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630714 | ||||||
| chr11:111630980
|
A | C | 1 | a0001c0001t0009g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.316+10578A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111630980 | ||||||
| chr11:111631126
|
G | C | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+10724G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631126 | ||||||
| chr11:111631216
|
G | A | 2 | a0001c0001t0011g0124a0001c0001t0011g0186 | 2 | HG01943.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.316+10814G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631216 | ||||||
| chr11:111631238
|
G | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+10836G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631238 | ||||||
| chr11:111631266
|
C | T | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316+10864C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631266 | ||||||
| chr11:111631479
|
T | G | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+11077T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631479 | ||||||
| chr11:111631526
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.316+11124G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631526 | ||||||
| chr11:111631664
|
C | G | 2 | a0001c0001t0020g0133a0001c0001t0020g0134 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.316+11262C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631664 | ||||||
| chr11:111631675
|
T | G | 1 | a0001c0001t0007g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.316+11273T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631675 | ||||||
| chr11:111631755
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+11353A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631755 | ||||||
| chr11:111631849
|
AG | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.316+11449delG | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111631849 | |||||
| chr11:111631962
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316+11560A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111631962 | ||||||
| chr11:111632402
|
T | A | 1 | a0001c0001t0017g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.316+12000T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111632402 | ||||||
| chr11:111632669
|
T | C | 1 | a0001c0001t0011g0027 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.316+12267T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111632669 | ||||||
| chr11:111632882
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.316+12480G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111632882 | ||||||
| chr11:111632883
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.316+12481A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111632883 | ||||||
| chr11:111633274
|
C | T | 1 | a0001c0001t0049g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.316+12872C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111633274 | ||||||
| chr11:111633360
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316+12958T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111633360 | ||||||
| chr11:111633583
|
T | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG00621.hp1 NA18939.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+13181T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111633583 | ||||||
| chr11:111633609
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.316+13207G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111633609 | ||||||
| chr11:111634053
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+13651G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634053 | ||||||
| chr11:111634137
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+13735C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634137 | ||||||
| chr11:111634197
|
TG | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+13796delG | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634197 | ||||||
| chr11:111634231
|
C | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+13829C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634231 | ||||||
| chr11:111634385
|
A | G | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.316+13983A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634385 | ||||||
| chr11:111634572
|
A | G | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+14170A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634572 | ||||||
| chr11:111634839
|
G | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+14437G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111634839 | ||||||
| chr11:111635040
|
C | T | 1 | a0001c0001t0013g0188 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.316+14638C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635040 | ||||||
| chr11:111635092
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+14690A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635092 | ||||||
| chr11:111635156
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+14754T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635156 | ||||||
| chr11:111635303
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+14901G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635303 | ||||||
| chr11:111635400
|
GA | G | 15 | a0001c0001t0002g0196a0001c0001t0004g0107a0001c0001t0004g0147others(12): Show | 15 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.316+15001delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111635400 | |||||
| chr11:111635411
|
AGGAGGGA others(28): Show |
A | 5 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+15024_316+1505 others(39): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111635411 | |||||
| chr11:111635440
|
AAGGG | A | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+15056_316+1505 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111635440 | |||||
| chr11:111635485
|
C | CAGAG | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.316+15083_316+1508 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635485 | ||||||
| chr11:111635712
|
G | C | 4 | a0001c0001t0037g0120a0001c0001t0047g0001a0001c0006t0025g0119others(1): Show | 4 | HG02109.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+15310G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111635712 | ||||||
| chr11:111636298
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+15896A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636298 | ||||||
| chr11:111636465
|
A | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.316+16063A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636465 | ||||||
| chr11:111636656
|
T | C | 7 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0111others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+16254T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636656 | ||||||
| chr11:111636708
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+16306C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636708 | ||||||
| chr11:111636880
|
G | T | 2 | a0001c0001t0008g0039a0001c0001t0008g0046 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.316+16478G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636880 | ||||||
| chr11:111636963
|
G | A | 1 | a0001c0001t0011g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.316+16561G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636963 | ||||||
| chr11:111636988
|
T | C | 2 | a0001c0001t0022g0008a0001c0001t0031g0009 | 2 | HG02056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.316+16586T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111636988 | ||||||
| chr11:111637279
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.316+16877A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637279 | ||||||
| chr11:111637374
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+16972A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637374 | ||||||
| chr11:111637387
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0072others(2): Show | 5 | HG00733.hp1 HG02523.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+16985A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637387 | ||||||
| chr11:111637407
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.316+17005C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637407 | ||||||
| chr11:111637408
|
G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.316+17006G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637408 | ||||||
| chr11:111637444
|
A | G | 3 | a0001c0001t0004g0147a0001c0001t0004g0150a0001c0001t0004g0151 | 3 | HG02723.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.316+17042A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637444 | ||||||
| chr11:111637456
|
C | CT | 12 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(9): Show | 12 | HG01952.hp2 HG02809.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+17075dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111637456 | |||||
| chr11:111637456
|
C | CTTTTTT | 6 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+17070_316+1707 others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111637456 | |||||
| chr11:111637523
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+17121A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637523 | ||||||
| chr11:111637542
|
C | T | 3 | a0001c0001t0008g0169a0001c0001t0008g0178a0001c0001t0017g0171 | 3 | HG02647.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.316+17140C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637542 | ||||||
| chr11:111637582
|
C | T | 4 | a0001c0001t0007g0108a0001c0001t0007g0112a0001c0001t0007g0113others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+17180C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637582 | ||||||
| chr11:111637587
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+17185G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637587 | ||||||
| chr11:111637611
|
C | G | 1 | a0001c0001t0045g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.316+17209C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637611 | ||||||
| chr11:111637746
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+17344G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637746 | ||||||
| chr11:111637926
|
C | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+17524C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111637926 | ||||||
| chr11:111638017
|
G | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+17615G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638017 | ||||||
| chr11:111638116
|
C | G | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+17714C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638116 | ||||||
| chr11:111638212
|
G | A | 9 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+17810G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638212 | ||||||
| chr11:111638270
|
G | C | 1 | a0001c0001t0007g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.316+17868G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638270 | ||||||
| chr11:111638792
|
C | A | 8 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0132others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+18390C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638792 | ||||||
| chr11:111638865
|
G | T | 9 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(6): Show | 9 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+18463G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638865 | ||||||
| chr11:111638877
|
T | G | 1 | a0001c0001t0027g0025 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.316+18475T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638877 | ||||||
| chr11:111638885
|
T | C | 3 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0038 | 3 | HG01496.hp2 HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.316+18483T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111638885 | ||||||
| chr11:111639003
|
G | A | 1 | a0001c0001t0005g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316+18601G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639003 | ||||||
| chr11:111639004
|
C | T | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+18602C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639004 | ||||||
| chr11:111639179
|
A | C | 6 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0112others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+18777A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639179 | ||||||
| chr11:111639233
|
C | T | 1 | a0001c0001t0041g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.316+18831C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639233 | ||||||
| chr11:111639249
|
G | C | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+18847G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639249 | ||||||
| chr11:111639257
|
A | AGCACCTC others(3): Show |
11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+18858_316+1885 others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111639257 | |||||
| chr11:111639378
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.316+18976A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639378 | ||||||
| chr11:111639623
|
C | G | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+19221C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639623 | ||||||
| chr11:111639732
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+19330C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639732 | ||||||
| chr11:111639736
|
C | T | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+19334C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639736 | ||||||
| chr11:111639845
|
G | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.316+19443G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111639845 | ||||||
| chr11:111640072
|
G | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+19670G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640072 | ||||||
| chr11:111640093
|
T | C | 1 | a0001c0001t0006g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.316+19691T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640093 | ||||||
| chr11:111640121
|
T | C | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.316+19719T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640121 | ||||||
| chr11:111640423
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+20021G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640423 | ||||||
| chr11:111640423
|
G | T | 3 | a0001c0001t0047g0001a0001c0006t0025g0119a0001c0007t0001g0198 | 3 | HG02109.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.316+20021G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640423 | ||||||
| chr11:111640675
|
C | T | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.316+20273C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640675 | ||||||
| chr11:111640693
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0055others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+20291G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640693 | ||||||
| chr11:111640722
|
A | AT | 54 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.316+20350dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
A | ATT | 19 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0023others(16): Show | 19 | HG00558.hp2 HG00642.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.316+20349_316+2035 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
A | ATTT | 10 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0059others(7): Show | 10 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+20348_316+2035 others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
AT | A | 32 | a0001c0001t0002g0196a0001c0001t0003g0159a0001c0001t0003g0167others(29): Show | 32 | HG00738.hp1 HG01099.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.316+20350delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
ATT | A | 54 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0180others(51): Show | 54 | HG00558.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.316+20349_316+2035 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
ATTT | A | 5 | a0001c0001t0053g0118a0001c0001t0061g0103a0001c0002t0003g0193others(2): Show | 5 | HG00099.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+20348_316+2035 others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0041g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.316+20340_316+2035 others(15): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0010g0079a0001c0001t0010g0081 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.316+20337_316+2035 others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640722
|
ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(2): Show | 5 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+20336_316+2035 others(19): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111640722 | |||||
| chr11:111640991
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+20589C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111640991 | ||||||
| chr11:111641015
|
A | G | 1 | a0001c0001t0017g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.316+20613A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641015 | ||||||
| chr11:111641236
|
A | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316+20834A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641236 | ||||||
| chr11:111641288
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+20886A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641288 | ||||||
| chr11:111641432
|
A | C | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+21030A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641432 | ||||||
| chr11:111641642
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.316+21240T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641642 | ||||||
| chr11:111641926
|
T | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.316+21524T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111641926 | ||||||
| chr11:111642142
|
G | A | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.316+21740G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642142 | ||||||
| chr11:111642147
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.316+21745G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642147 | ||||||
| chr11:111642186
|
T | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+21784T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642186 | ||||||
| chr11:111642240
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+21838G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642240 | ||||||
| chr11:111642276
|
C | G | 10 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(7): Show | 10 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+21874C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642276 | ||||||
| chr11:111642331
|
T | A | 1 | a0001c0001t0002g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.316+21929T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642331 | ||||||
| chr11:111642543
|
C | G | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.316+22141C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642543 | ||||||
| chr11:111642643
|
G | A | 1 | a0001c0001t0058g0010 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.316+22241G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642643 | ||||||
| chr11:111642729
|
A | G | 1 | a0001c0001t0009g0166 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.316+22327A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642729 | ||||||
| chr11:111642824
|
G | GGGCTTGT others(37): Show |
9 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0018g0140others(6): Show | 9 | HG02109.hp2 HG02886.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+22459_316+2246 others(48): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111642824 | |||||
| chr11:111642824
|
G | GGGCTTGT others(81): Show |
2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+22459_316+2246 others(92): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111642824 | |||||
| chr11:111642852
|
C | G | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0038others(1): Show | 4 | HG01496.hp2 HG01975.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+22450C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642852 | ||||||
| chr11:111642866
|
A | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+22464A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642866 | ||||||
| chr11:111642879
|
T | C | 1 | a0001c0001t0058g0010 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.316+22477T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642879 | ||||||
| chr11:111642921
|
T | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.316+22519T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642921 | ||||||
| chr11:111642940
|
C | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+22538C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111642940 | ||||||
| chr11:111643186
|
C | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+22784C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111643186 | ||||||
| chr11:111643305
|
T | C | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+22903T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111643305 | ||||||
| chr11:111643464
|
T | TA | 7 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(4): Show | 7 | HG00733.hp2 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+23074dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111643464 | |||||
| chr11:111643476
|
A | AG | 3 | a0001c0001t0037g0120a0001c0006t0025g0119a0001c0007t0001g0198 | 3 | HG02109.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.316+23075dupG | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111643476 | |||||
| chr11:111643498
|
A | G | 1 | a0001c0001t0032g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.316+23096A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111643498 | ||||||
| chr11:111643577
|
G | A | 1 | a0001c0001t0030g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+23175G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111643577 | ||||||
| chr11:111644023
|
A | C | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+23621A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644023 | ||||||
| chr11:111644026
|
A | G | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+23624A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644026 | ||||||
| chr11:111644084
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316+23682G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644084 | ||||||
| chr11:111644123
|
T | A | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.316+23721T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644123 | ||||||
| chr11:111644221
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+23819G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644221 | ||||||
| chr11:111644245
|
C | T | 9 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+23843C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644245 | ||||||
| chr11:111644246
|
G | A | 2 | a0001c0001t0022g0008a0001c0001t0031g0009 | 2 | HG02056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.316+23844G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644246 | ||||||
| chr11:111644266
|
C | A | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+23864C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644266 | ||||||
| chr11:111644287
|
CA | C | 6 | a0001c0001t0001g0105a0001c0001t0003g0163a0001c0001t0003g0187others(3): Show | 6 | HG01070.hp2 HG01169.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+23902delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111644287 | |||||
| chr11:111644301
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0005g0144a0001c0001t0008g0176others(3): Show | 6 | HG01109.hp2 HG01261.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+23899A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644301 | ||||||
| chr11:111644335
|
T | C | 9 | a0001c0001t0001g0093a0001c0001t0012g0031a0001c0001t0012g0032others(6): Show | 9 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+23933T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644335 | ||||||
| chr11:111644337
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.316+23935C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644337 | ||||||
| chr11:111644460
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.316+24058G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644460 | ||||||
| chr11:111644467
|
G | A | 1 | a0001c0001t0050g0185 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.316+24065G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644467 | ||||||
| chr11:111644593
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+24191T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644593 | ||||||
| chr11:111644777
|
A | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+24375A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644777 | ||||||
| chr11:111644822
|
A | G | 1 | a0001c0001t0008g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.316+24420A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644822 | ||||||
| chr11:111644823
|
T | C | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+24421T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644823 | ||||||
| chr11:111644918
|
T | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+24516T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111644918 | ||||||
| chr11:111645205
|
T | C | 8 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(5): Show | 8 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+24803T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645205 | ||||||
| chr11:111645225
|
A | G | 4 | a0001c0001t0007g0108a0001c0001t0007g0112a0001c0001t0007g0113others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+24823A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645225 | ||||||
| chr11:111645316
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.316+24914T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645316 | ||||||
| chr11:111645507
|
G | A | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.316+25105G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645507 | ||||||
| chr11:111645588
|
A | G | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+25186A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645588 | ||||||
| chr11:111645636
|
C | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0092a0001c0001t0002g0006others(18): Show | 21 | HG01070.hp1 HG01255.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+25234C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645636 | ||||||
| chr11:111645779
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.316+25377C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645779 | ||||||
| chr11:111645805
|
GA | G | 7 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(4): Show | 7 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+25415delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111645805 | |||||
| chr11:111645866
|
C | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.316+25464C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645866 | ||||||
| chr11:111645981
|
A | G | 1 | a0001c0001t0054g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316+25579A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111645981 | ||||||
| chr11:111646056
|
A | G | 4 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+25654A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646056 | ||||||
| chr11:111646081
|
C | CGCGCACA others(13): Show |
2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+25680_316+2569 others(24): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111646081 | |||||
| chr11:111646170
|
C | T | 2 | a0001c0001t0054g0141a0001c0001t0055g0142 | 2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.316+25768C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646170 | ||||||
| chr11:111646171
|
C | T | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.316+25769C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646171 | ||||||
| chr11:111646172
|
G | A | 9 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(6): Show | 9 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+25770G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646172 | ||||||
| chr11:111646276
|
C | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.316+25874C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646276 | ||||||
| chr11:111646278
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+25876C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646278 | ||||||
| chr11:111646317
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316+25915C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646317 | ||||||
| chr11:111646758
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.316+26356T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111646758 | ||||||
| chr11:111647176
|
G | A | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+26774G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647176 | ||||||
| chr11:111647184
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+26782G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647184 | ||||||
| chr11:111647242
|
T | C | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+26840T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647242 | ||||||
| chr11:111647263
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.316+26861G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647263 | ||||||
| chr11:111647478
|
C | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+27076C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647478 | ||||||
| chr11:111647551
|
AC | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.316+27154delC | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111647551 | |||||
| chr11:111647562
|
GA | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.316+27180delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111647562 | |||||
| chr11:111647562
|
GAA | G | 14 | a0001c0001t0001g0043a0001c0001t0010g0077a0001c0001t0010g0078others(11): Show | 14 | HG00140.hp1 HG01070.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.316+27179_316+2718 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111647562 | |||||
| chr11:111647592
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.316+27190C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647592 | ||||||
| chr11:111647651
|
G | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+27249G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647651 | ||||||
| chr11:111647728
|
C | T | 1 | a0001c0001t0012g0032 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.316+27326C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647728 | ||||||
| chr11:111647729
|
G | A | 2 | a0001c0001t0003g0182a0001c0003t0003g0195 | 2 | HG02004.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.316+27327G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647729 | ||||||
| chr11:111647867
|
C | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+27465C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111647867 | ||||||
| chr11:111648039
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+27637A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111648039 | ||||||
| chr11:111648276
|
ATACCT | A | 26 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(23): Show | 26 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+27877_316+2788 others(9): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111648276 | |||||
| chr11:111648421
|
G | A | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+28019G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111648421 | ||||||
| chr11:111648489
|
A | G | 1 | a0001c0001t0011g0029 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.316+28087A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111648489 | ||||||
| chr11:111649021
|
A | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+28619A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649021 | ||||||
| chr11:111649392
|
G | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+28990G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649392 | ||||||
| chr11:111649700
|
G | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+29298G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649700 | ||||||
| chr11:111649701
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+29299C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649701 | ||||||
| chr11:111649798
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+29396A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649798 | ||||||
| chr11:111649861
|
A | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+29459A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649861 | ||||||
| chr11:111649876
|
T | A | 19 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.316+29474T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649876 | ||||||
| chr11:111649884
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.316+29482T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111649884 | ||||||
| chr11:111650065
|
T | A | 9 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+29663T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111650065 | ||||||
| chr11:111650279
|
C | T | 5 | a0001c0001t0011g0026a0001c0001t0011g0027a0001c0001t0011g0029others(2): Show | 5 | HG00140.hp2 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+29877C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111650279 | ||||||
| chr11:111650306
|
T | G | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+29904T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111650306 | ||||||
| chr11:111650590
|
A | AT | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+30189dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111650590 | |||||
| chr11:111650755
|
C | T | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316+30353C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111650755 | ||||||
| chr11:111651033
|
C | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.316+30631C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651033 | ||||||
| chr11:111651177
|
G | A | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+30775G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651177 | ||||||
| chr11:111651463
|
T | C | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+31061T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651463 | ||||||
| chr11:111651466
|
G | A | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+31064G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651466 | ||||||
| chr11:111651511
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+31109A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651511 | ||||||
| chr11:111651743
|
CATTT | C | 60 | a0001c0001t0002g0180a0001c0001t0002g0196a0001c0001t0003g0125others(57): Show | 60 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.316+31343_316+3134 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111651743 | |||||
| chr11:111651757
|
G | A | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+31355G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651757 | ||||||
| chr11:111651815
|
G | T | 2 | a0001c0001t0011g0027a0001c0001t0038g0028 | 2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.316+31413G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111651815 | ||||||
| chr11:111652295
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.316+31893G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652295 | ||||||
| chr11:111652356
|
A | G | 11 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+31954A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652356 | ||||||
| chr11:111652681
|
T | C | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.316+32279T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652681 | ||||||
| chr11:111652745
|
A | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG01109.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.316+32343A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652745 | ||||||
| chr11:111652775
|
T | G | 4 | a0001c0001t0037g0120a0001c0001t0047g0001a0001c0006t0025g0119others(1): Show | 4 | HG02109.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+32373T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652775 | ||||||
| chr11:111652829
|
A | G | 2 | a0001c0001t0011g0026a0001c0001t0011g0029 | 2 | HG00140.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.316+32427A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652829 | ||||||
| chr11:111652917
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316+32515T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111652917 | ||||||
| chr11:111653085
|
C | T | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+32683C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111653085 | ||||||
| chr11:111653166
|
G | A | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316+32764G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111653166 | ||||||
| chr11:111653367
|
G | T | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+32965G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111653367 | ||||||
| chr11:111653585
|
C | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+33183C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111653585 | ||||||
| chr11:111654096
|
A | G | 1 | a0001c0001t0030g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+33694A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654096 | ||||||
| chr11:111654290
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.317-33711A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654290 | ||||||
| chr11:111654345
|
T | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0019others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.317-33656T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654345 | ||||||
| chr11:111654398
|
A | C | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.317-33603A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654398 | ||||||
| chr11:111654456
|
G | A | 1 | a0001c0001t0059g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.317-33545G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654456 | ||||||
| chr11:111654630
|
A | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-33371A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654630 | ||||||
| chr11:111654842
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-33159A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654842 | ||||||
| chr11:111654969
|
T | A | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-33032T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654969 | ||||||
| chr11:111654984
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-33017A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111654984 | ||||||
| chr11:111655040
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-32961A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655040 | ||||||
| chr11:111655126
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-32875G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655126 | ||||||
| chr11:111655335
|
C | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-32666C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655335 | ||||||
| chr11:111655340
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.317-32661G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655340 | ||||||
| chr11:111655687
|
T | C | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-32314T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655687 | ||||||
| chr11:111655901
|
G | C | 5 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-32100G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111655901 | ||||||
| chr11:111656023
|
CA | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.317-31960delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111656023 | |||||
| chr11:111656738
|
A | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.317-31263A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111656738 | ||||||
| chr11:111656905
|
G | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-31096G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111656905 | ||||||
| chr11:111656948
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.317-31053A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111656948 | ||||||
| chr11:111656953
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.317-31048C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111656953 | ||||||
| chr11:111656997
|
T | C | 4 | a0001c0001t0007g0108a0001c0001t0007g0112a0001c0001t0007g0113others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-31004T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111656997 | ||||||
| chr11:111657013
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-30988T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657013 | ||||||
| chr11:111657014
|
A | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 10 | HG00621.hp1 HG01934.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.317-30987A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657014 | ||||||
| chr11:111657051
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.317-30950T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657051 | ||||||
| chr11:111657057
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.317-30944A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657057 | ||||||
| chr11:111657141
|
A | C | 1 | a0001c0001t0024g0197 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.317-30860A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657141 | ||||||
| chr11:111657154
|
T | C | 2 | a0001c0001t0022g0008a0001c0001t0031g0009 | 2 | HG02056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.317-30847T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657154 | ||||||
| chr11:111657609
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-30392G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657609 | ||||||
| chr11:111657631
|
C | T | 2 | a0001c0001t0005g0129a0001c0001t0005g0139 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.317-30370C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657631 | ||||||
| chr11:111657681
|
G | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-30320G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657681 | ||||||
| chr11:111657687
|
C | G | 1 | a0001c0001t0003g0187 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.317-30314C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657687 | ||||||
| chr11:111657717
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.317-30284A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657717 | ||||||
| chr11:111657739
|
G | C | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-30262G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657739 | ||||||
| chr11:111657949
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.317-30052A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111657949 | ||||||
| chr11:111658062
|
A | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.317-29939A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658062 | ||||||
| chr11:111658090
|
TTTTA | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(66): Show | 69 | HG00558.hp2 HG00733.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.317-29863_317-2986 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111658090 | |||||
| chr11:111658090
|
TTTTATTT others(1): Show |
T | 68 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0058others(65): Show | 68 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.317-29867_317-2986 others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111658090 | |||||
| chr11:111658090
|
TTTTATTT others(5): Show |
T | 15 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0002g0020others(12): Show | 15 | HG00140.hp1 HG00642.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-29871_317-2986 others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111658090 | |||||
| chr11:111658090
|
TTTTATTT others(9): Show |
T | 4 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0022g0008others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-29875_317-2986 others(20): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111658090 | |||||
| chr11:111658090
|
TTTTATTT others(13): Show |
T | 3 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0061g0103 | 3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-29879_317-2986 others(24): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111658090 | |||||
| chr11:111658102
|
A | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-29899A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658102 | ||||||
| chr11:111658187
|
G | A | 45 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(42): Show | 45 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.317-29814G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658187 | ||||||
| chr11:111658359
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-29642G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658359 | ||||||
| chr11:111658461
|
G | A | 1 | a0001c0001t0013g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.317-29540G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658461 | ||||||
| chr11:111658602
|
G | A | 15 | a0001c0001t0002g0196a0001c0001t0004g0107a0001c0001t0004g0147others(12): Show | 15 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.317-29399G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658602 | ||||||
| chr11:111658667
|
G | T | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-29334G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658667 | ||||||
| chr11:111658685
|
G | A | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.317-29316G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658685 | ||||||
| chr11:111658747
|
A | G | 9 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-29254A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658747 | ||||||
| chr11:111658775
|
A | G | 1 | a0001c0003t0003g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.317-29226A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111658775 | ||||||
| chr11:111659105
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.317-28896A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659105 | ||||||
| chr11:111659220
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.317-28781T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659220 | ||||||
| chr11:111659257
|
G | A | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.317-28744G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659257 | ||||||
| chr11:111659582
|
G | A | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0037g0120 | 3 | HG00733.hp2 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.317-28419G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659582 | ||||||
| chr11:111659611
|
C | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-28390C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659611 | ||||||
| chr11:111659612
|
G | A | 2 | a0001c0001t0011g0027a0001c0001t0038g0028 | 2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.317-28389G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659612 | ||||||
| chr11:111659622
|
T | TTTTTTAA others(320): Show |
1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317-28364_317-2836 others(331): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111659622 | |||||
| chr11:111659622
|
T | TTTTTTAA others(321): Show |
2 | a0001c0001t0037g0120a0001c0001t0047g0001 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.317-28364_317-2836 others(332): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111659622 | |||||
| chr11:111659622
|
T | TTTTTTAA others(322): Show |
1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-28364_317-2836 others(333): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111659622 | |||||
| chr11:111659634
|
C | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-28367C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659634 | ||||||
| chr11:111659729
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-28272A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659729 | ||||||
| chr11:111659883
|
C | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-28118C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659883 | ||||||
| chr11:111659921
|
C | T | 1 | a0001c0001t0062g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.317-28080C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111659921 | ||||||
| chr11:111660026
|
T | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-27975T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660026 | ||||||
| chr11:111660031
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.317-27970G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660031 | ||||||
| chr11:111660349
|
CTCT | C | 4 | a0001c0001t0001g0021a0001c0001t0002g0012a0001c0001t0002g0030others(1): Show | 4 | HG01255.hp2 HG03017.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-27645_317-2764 others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111660349 | |||||
| chr11:111660445
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.317-27556T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660445 | ||||||
| chr11:111660547
|
A | ACCAGGTA others(30): Show |
1 | a0001c0001t0006g0090 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.317-27454_317-2745 others(41): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660547 | ||||||
| chr11:111660548
|
A | T | 1 | a0001c0001t0006g0090 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.317-27453A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660548 | ||||||
| chr11:111660839
|
C | CT | 36 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(33): Show | 36 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.317-27137dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111660839 | |||||
| chr11:111660839
|
CT | C | 19 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0004g0107others(16): Show | 19 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.317-27137delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111660839 | |||||
| chr11:111660839
|
CTT | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0069others(18): Show | 21 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.317-27138_317-2713 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111660839 | |||||
| chr11:111660839
|
CTTT | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.317-27139_317-2713 others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111660839 | |||||
| chr11:111660872
|
G | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-27129G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660872 | ||||||
| chr11:111660985
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-27016C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660985 | ||||||
| chr11:111660989
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.317-27012G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111660989 | ||||||
| chr11:111661594
|
A | C | 2 | a0001c0001t0019g0094a0001c0001t0019g0095 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.317-26407A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661594 | ||||||
| chr11:111661659
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-26342T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661659 | ||||||
| chr11:111661718
|
A | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.317-26283A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661718 | ||||||
| chr11:111661749
|
A | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.317-26252A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661749 | ||||||
| chr11:111661760
|
C | A | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-26241C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661760 | ||||||
| chr11:111661885
|
G | T | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.317-26116G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661885 | ||||||
| chr11:111661967
|
C | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.317-26034C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111661967 | ||||||
| chr11:111662070
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.317-25931C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662070 | ||||||
| chr11:111662142
|
A | T | 1 | a0001c0001t0001g0002 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.317-25859A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662142 | ||||||
| chr11:111662257
|
A | G | 1 | a0001c0001t0044g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.317-25744A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662257 | ||||||
| chr11:111662257
|
A | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-25744A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662257 | ||||||
| chr11:111662351
|
C | T | 6 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG01952.hp2 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-25650C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662351 | ||||||
| chr11:111662381
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-25620C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662381 | ||||||
| chr11:111662711
|
T | C | 3 | a0001c0001t0008g0169a0001c0001t0008g0178a0001c0001t0017g0171 | 3 | HG02647.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.317-25290T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662711 | ||||||
| chr11:111662864
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.317-25137G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111662864 | ||||||
| chr11:111663185
|
A | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-24816A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663185 | ||||||
| chr11:111663224
|
C | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-24777C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663224 | ||||||
| chr11:111663232
|
CA | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.317-24754delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111663232 | |||||
| chr11:111663232
|
CAA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0019g0094others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-24755_317-2475 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111663232 | |||||
| chr11:111663258
|
A | C | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-24743A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663258 | ||||||
| chr11:111663302
|
T | C | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.317-24699T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663302 | ||||||
| chr11:111663472
|
A | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0055others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-24529A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663472 | ||||||
| chr11:111663473
|
G | A | 1 | a0001c0004t0042g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.317-24528G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663473 | ||||||
| chr11:111663585
|
A | G | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.317-24416A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663585 | ||||||
| chr11:111663609
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.317-24392T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663609 | ||||||
| chr11:111663712
|
C | T | 1 | a0001c0001t0044g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.317-24289C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663712 | ||||||
| chr11:111663718
|
T | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.317-24283T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663718 | ||||||
| chr11:111663813
|
G | C | 1 | a0001c0001t0004g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.317-24188G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663813 | ||||||
| chr11:111663961
|
C | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-24040C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111663961 | ||||||
| chr11:111664058
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.317-23943C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664058 | ||||||
| chr11:111664088
|
C | A | 1 | a0001c0001t0010g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.317-23913C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664088 | ||||||
| chr11:111664251
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-23750A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664251 | ||||||
| chr11:111664341
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-23660G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664341 | ||||||
| chr11:111664350
|
C | T | 10 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(7): Show | 10 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-23651C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664350 | ||||||
| chr11:111664378
|
G | A | 43 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.317-23623G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664378 | ||||||
| chr11:111664381
|
C | T | 43 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.317-23620C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664381 | ||||||
| chr11:111664488
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-23513C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664488 | ||||||
| chr11:111664589
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-23412G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664589 | ||||||
| chr11:111664698
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.317-23303C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664698 | ||||||
| chr11:111664827
|
C | T | 8 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-23174C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664827 | ||||||
| chr11:111664833
|
T | G | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0060g0102others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-23168T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111664833 | ||||||
| chr11:111665258
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-22743C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665258 | ||||||
| chr11:111665282
|
C | CA | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-22707dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111665282 | |||||
| chr11:111665466
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.317-22535G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665466 | ||||||
| chr11:111665519
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.317-22482A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665519 | ||||||
| chr11:111665543
|
G | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-22458G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665543 | ||||||
| chr11:111665748
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-22253C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665748 | ||||||
| chr11:111665751
|
G | T | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-22250G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665751 | ||||||
| chr11:111665752
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.317-22249G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665752 | ||||||
| chr11:111665856
|
GA | G | 6 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0017g0189others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-22134delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111665856 | |||||
| chr11:111665921
|
T | C | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-22080T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665921 | ||||||
| chr11:111665946
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-22055G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665946 | ||||||
| chr11:111665997
|
A | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-22004A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665997 | ||||||
| chr11:111665999
|
G | A | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.317-22002G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111665999 | ||||||
| chr11:111666029
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-21972C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666029 | ||||||
| chr11:111666212
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-21789C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666212 | ||||||
| chr11:111666213
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-21788G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666213 | ||||||
| chr11:111666369
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.317-21632G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666369 | ||||||
| chr11:111666411
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0039g0143 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.317-21590T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666411 | ||||||
| chr11:111666477
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0039g0143 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.317-21524T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111666477 | ||||||
| chr11:111666943
|
T | TTTTA | 13 | a0001c0001t0001g0105a0001c0001t0004g0107a0001c0001t0004g0152others(10): Show | 13 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.317-21019_317-2101 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111666943
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0150others(4): Show | 7 | HG01952.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-21023_317-2101 others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111666943
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0004g0147a0001c0001t0004g0151 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-21027_317-2101 others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111666943
|
TTTTA | T | 14 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-21019_317-2101 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111666943
|
TTTTATTT others(1): Show |
T | 4 | a0001c0001t0001g0106a0001c0001t0002g0180a0001c0001t0026g0104others(1): Show | 4 | HG02129.hp2 HG02145.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-21023_317-2101 others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111666943
|
TTTTATTT others(5): Show |
T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-21027_317-2101 others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111666943 | |||||
| chr11:111667044
|
C | T | 10 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(7): Show | 10 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-20957C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667044 | ||||||
| chr11:111667045
|
G | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-20956G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667045 | ||||||
| chr11:111667145
|
C | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-20856C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667145 | ||||||
| chr11:111667464
|
T | C | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.317-20537T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667464 | ||||||
| chr11:111667488
|
CT | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.317-20492delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111667488 | |||||
| chr11:111667517
|
G | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-20484G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667517 | ||||||
| chr11:111667531
|
G | A | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.317-20470G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667531 | ||||||
| chr11:111667588
|
C | T | 1 | a0001c0001t0011g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.317-20413C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667588 | ||||||
| chr11:111667658
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-20343T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111667658 | ||||||
| chr11:111668151
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.317-19850T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668151 | ||||||
| chr11:111668176
|
A | AGG | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-19824_317-1982 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668176 | |||||
| chr11:111668177
|
G | GGGGT | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.317-19823_317-1982 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668177 | |||||
| chr11:111668177
|
G | GGGGTGT | 17 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0055others(14): Show | 17 | HG00558.hp2 HG01070.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.317-19823_317-1982 others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668177 | |||||
| chr11:111668177
|
GGA | G | 3 | a0001c0001t0018g0140a0001c0001t0026g0104a0002c0005t0018g0101 | 3 | HG03130.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-19822_317-1982 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668177 | |||||
| chr11:111668179
|
A | AGT | 59 | a0001c0001t0001g0105a0001c0001t0002g0180a0001c0001t0003g0125others(56): Show | 59 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.317-19797_317-1979 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668179 | |||||
| chr11:111668179
|
A | AGTGT | 18 | a0001c0001t0001g0106a0001c0001t0005g0126a0001c0001t0005g0127others(15): Show | 18 | HG00738.hp1 HG01099.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.317-19799_317-1979 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668179 | |||||
| chr11:111668179
|
A | AGTGTGT | 2 | a0001c0001t0007g0109a0001c0001t0007g0115 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.317-19801_317-1979 others(10): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668179 | |||||
| chr11:111668179
|
A | G | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0046g0052 | 3 | HG00733.hp2 HG01099.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.317-19822A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668179 | ||||||
| chr11:111668179
|
A | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.317-19822A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668179 | ||||||
| chr11:111668179
|
AGT | A | 5 | a0001c0001t0002g0196a0001c0001t0008g0169a0001c0001t0008g0178others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-19797_317-1979 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111668179 | |||||
| chr11:111668181
|
T | G | 3 | a0001c0001t0018g0140a0001c0001t0026g0104a0002c0005t0018g0101 | 3 | HG03130.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-19820T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668181 | ||||||
| chr11:111668256
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-19745C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668256 | ||||||
| chr11:111668486
|
T | C | 1 | a0001c0001t0036g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.317-19515T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668486 | ||||||
| chr11:111668603
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-19398A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668603 | ||||||
| chr11:111668708
|
T | A | 2 | a0001c0001t0003g0182a0001c0003t0003g0195 | 2 | HG02004.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.317-19293T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668708 | ||||||
| chr11:111668834
|
T | A | 2 | a0001c0001t0009g0170a0001c0001t0009g0179 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.317-19167T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668834 | ||||||
| chr11:111668919
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-19082G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111668919 | ||||||
| chr11:111669075
|
G | A | 1 | a0001c0001t0006g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.317-18926G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669075 | ||||||
| chr11:111669151
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-18850A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669151 | ||||||
| chr11:111669563
|
C | G | 2 | a0001c0002t0003g0193a0001c0002t0034g0194 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.317-18438C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669563 | ||||||
| chr11:111669574
|
G | A | 7 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0015g0099others(4): Show | 7 | HG00733.hp2 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-18427G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669574 | ||||||
| chr11:111669649
|
A | G | 2 | a0001c0001t0003g0165a0001c0001t0033g0174 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.317-18352A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669649 | ||||||
| chr11:111669713
|
G | A | 12 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-18288G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111669713 | ||||||
| chr11:111670068
|
C | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-17933C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670068 | ||||||
| chr11:111670071
|
C | A | 2 | a0001c0001t0008g0178a0001c0001t0017g0171 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.317-17930C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670071 | ||||||
| chr11:111670133
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.317-17868T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670133 | ||||||
| chr11:111670299
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-17702G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670299 | ||||||
| chr11:111670323
|
A | G | 1 | a0001c0001t0006g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.317-17678A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670323 | ||||||
| chr11:111670400
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-17601A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670400 | ||||||
| chr11:111670411
|
T | C | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-17590T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670411 | ||||||
| chr11:111670457
|
G | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-17544G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670457 | ||||||
| chr11:111670532
|
G | A | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-17469G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670532 | ||||||
| chr11:111670731
|
A | C | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.317-17270A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670731 | ||||||
| chr11:111670800
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317-17201A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670800 | ||||||
| chr11:111670895
|
T | C | 5 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0018g0140others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-17106T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670895 | ||||||
| chr11:111670962
|
C | T | 2 | a0001c0001t0037g0120a0001c0001t0047g0001 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.317-17039C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111670962 | ||||||
| chr11:111671124
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.317-16877A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671124 | ||||||
| chr11:111671247
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-16754G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671247 | ||||||
| chr11:111671545
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-16456A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671545 | ||||||
| chr11:111671619
|
C | A | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-16382C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671619 | ||||||
| chr11:111671782
|
A | G | 21 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0041others(18): Show | 21 | HG00621.hp1 HG01192.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.317-16219A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671782 | ||||||
| chr11:111671964
|
G | A | 2 | a0001c0001t0008g0039a0001c0001t0008g0046 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.317-16037G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111671964 | ||||||
| chr11:111672031
|
G | T | 10 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(7): Show | 10 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-15970G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672031 | ||||||
| chr11:111672126
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.317-15875G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672126 | ||||||
| chr11:111672185
|
T | A | 1 | a0001c0001t0063g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.317-15816T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672185 | ||||||
| chr11:111672205
|
C | A | 1 | a0001c0001t0002g0038 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.317-15796C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672205 | ||||||
| chr11:111672328
|
G | A | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-15673G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672328 | ||||||
| chr11:111672352
|
A | C | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-15649A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672352 | ||||||
| chr11:111672390
|
C | T | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-15611C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672390 | ||||||
| chr11:111672493
|
G | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-15508G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672493 | ||||||
| chr11:111672579
|
T | A | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02055.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-15422T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672579 | ||||||
| chr11:111672707
|
T | A | 1 | a0001c0001t0003g0187 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.317-15294T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111672707 | ||||||
| chr11:111672841
|
A | AT | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-15158dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111672841 | |||||
| chr11:111673049
|
C | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-14952C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673049 | ||||||
| chr11:111673122
|
A | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-14879A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673122 | ||||||
| chr11:111673192
|
T | A | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.317-14809T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673192 | ||||||
| chr11:111673623
|
A | G | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-14378A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673623 | ||||||
| chr11:111673811
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.317-14190A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673811 | ||||||
| chr11:111673860
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.317-14141G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673860 | ||||||
| chr11:111673944
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.317-14057C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673944 | ||||||
| chr11:111673974
|
T | G | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-14027T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111673974 | ||||||
| chr11:111674034
|
G | A | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.317-13967G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674034 | ||||||
| chr11:111674034
|
G | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.317-13967G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674034 | ||||||
| chr11:111674071
|
TA | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.317-13918delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111674071 | |||||
| chr11:111674098
|
A | G | 1 | a0001c0001t0012g0032 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.317-13903A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674098 | ||||||
| chr11:111674154
|
G | A | 2 | a0001c0001t0004g0154a0001c0001t0004g0155 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.317-13847G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674154 | ||||||
| chr11:111674194
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.317-13807G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674194 | ||||||
| chr11:111674232
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0056g0146 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.317-13769A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674232 | ||||||
| chr11:111674564
|
A | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.317-13437A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674564 | ||||||
| chr11:111674669
|
G | A | 5 | a0001c0001t0011g0026a0001c0001t0011g0027a0001c0001t0011g0029others(2): Show | 5 | HG00140.hp2 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-13332G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111674669 | ||||||
| chr11:111675296
|
C | T | 5 | a0001c0001t0011g0026a0001c0001t0011g0027a0001c0001t0011g0029others(2): Show | 5 | HG00140.hp2 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-12705C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675296 | ||||||
| chr11:111675302
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.317-12699A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675302 | ||||||
| chr11:111675314
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-12687G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675314 | ||||||
| chr11:111675392
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317-12609A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675392 | ||||||
| chr11:111675480
|
A | T | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-12521A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675480 | ||||||
| chr11:111675699
|
T | C | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-12302T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111675699 | ||||||
| chr11:111676435
|
C | A | 1 | a0001c0001t0002g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.317-11566C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111676435 | ||||||
| chr11:111676748
|
C | T | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-11253C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111676748 | ||||||
| chr11:111677103
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-10898G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111677103 | ||||||
| chr11:111677206
|
G | T | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-10795G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111677206 | ||||||
| chr11:111677434
|
TG | T | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-10565delG | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111677434 | |||||
| chr11:111677523
|
T | G | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-10478T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111677523 | ||||||
| chr11:111677562
|
C | T | 2 | a0001c0001t0007g0112a0001c0001t0007g0114 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.317-10439C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111677562 | ||||||
| chr11:111677586
|
A | AT | 160 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0019others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.317-10393dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111677586 | |||||
| chr11:111677586
|
A | ATT | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0049others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.317-10394_317-1039 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111677586 | |||||
| chr11:111677824
|
T | C | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317-10177T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111677824 | ||||||
| chr11:111678215
|
C | A | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-9786C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678215 | ||||||
| chr11:111678269
|
C | A | 1 | a0001c0001t0023g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.317-9732C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678269 | ||||||
| chr11:111678354
|
G | A | 5 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-9647G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678354 | ||||||
| chr11:111678418
|
G | A | 1 | a0001c0001t0061g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.317-9583G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678418 | ||||||
| chr11:111678521
|
T | C | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-9480T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678521 | ||||||
| chr11:111678679
|
C | G | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-9322C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678679 | ||||||
| chr11:111678853
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0039g0143 | 3 | HG02145.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.317-9148C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111678853 | ||||||
| chr11:111679467
|
G | A | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.317-8534G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111679467 | ||||||
| chr11:111679955
|
T | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-8046T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111679955 | ||||||
| chr11:111680131
|
A | G | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-7870A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111680131 | ||||||
| chr11:111680487
|
C | A | 1 | a0001c0001t0032g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.317-7514C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111680487 | ||||||
| chr11:111680567
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.317-7434T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111680567 | ||||||
| chr11:111680767
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.317-7234G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111680767 | ||||||
| chr11:111681123
|
G | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.317-6878G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681123 | ||||||
| chr11:111681268
|
G | A | 1 | a0001c0001t0057g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.317-6733G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681268 | ||||||
| chr11:111681299
|
T | C | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-6702T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681299 | ||||||
| chr11:111681329
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.317-6672A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681329 | ||||||
| chr11:111681737
|
A | G | 4 | a0001c0001t0015g0099a0001c0001t0015g0100a0001c0001t0060g0102others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-6264A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681737 | ||||||
| chr11:111681833
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317-6168A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681833 | ||||||
| chr11:111681930
|
A | T | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-6071A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681930 | ||||||
| chr11:111681990
|
G | A | 1 | a0001c0001t0059g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.317-6011G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111681990 | ||||||
| chr11:111682064
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.317-5937T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682064 | ||||||
| chr11:111682170
|
C | T | 12 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(9): Show | 12 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-5831C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682170 | ||||||
| chr11:111682189
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.317-5812A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682189 | ||||||
| chr11:111682350
|
G | C | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-5651G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682350 | ||||||
| chr11:111682614
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0041g0073a0001c0001t0048g0071 | 3 | HG00733.hp1 HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.317-5387T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682614 | ||||||
| chr11:111682673
|
G | A | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.317-5328G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682673 | ||||||
| chr11:111682762
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-5239C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111682762 | ||||||
| chr11:111683169
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.317-4832T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683169 | ||||||
| chr11:111683213
|
C | G | 1 | a0001c0001t0018g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.317-4788C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683213 | ||||||
| chr11:111683307
|
A | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-4694A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683307 | ||||||
| chr11:111683451
|
T | A | 1 | a0001c0001t0002g0017 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.317-4550T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683451 | ||||||
| chr11:111683844
|
T | C | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-4157T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683844 | ||||||
| chr11:111683996
|
C | T | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.317-4005C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111683996 | ||||||
| chr11:111684081
|
TCA | T | 11 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(8): Show | 11 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-3916_317-3915d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111684081 | |||||
| chr11:111684132
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0029g0097 | 2 | HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.317-3869C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111684132 | ||||||
| chr11:111684505
|
C | T | 6 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG01952.hp2 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-3496C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111684505 | ||||||
| chr11:111685072
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.317-2929C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111685072 | ||||||
| chr11:111685344
|
C | A | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.317-2657C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111685344 | ||||||
| chr11:111686269
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0002g0091 | 2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.317-1732C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111686269 | ||||||
| chr11:111686418
|
G | T | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.317-1583G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111686418 | ||||||
| chr11:111687447
|
G | A | 3 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166 | 3 | HG01891.hp2 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-554G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111687447 | ||||||
| chr11:111687514
|
C | CA | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.317-474dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111687514 | |||||
| chr11:111687603
|
T | TA | 11 | a0001c0001t0001g0093a0001c0001t0012g0031a0001c0001t0012g0032others(8): Show | 11 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-387dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111687603 | |||||
| chr11:111687604
|
A | T | 2 | a0001c0001t0053g0118a0001c0002t0034g0194 | 2 | HG00642.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.317-397A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111687604 | ||||||
| chr11:111687615
|
C | CT | 12 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-376dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111687615 | |||||
| chr11:111687642
|
C | CTG | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.317-358_317-357ins others(2): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 111687642 | |||||
| chr11:111687645
|
G | A | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.317-356G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111687645 | ||||||
| chr11:111687954
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.317-47G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111687954 | ||||||
| chr11:111687955
|
T | C | 1 | a0001c0001t0014g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.317-46T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 3/14 | chr11 | 111687955 | ||||||
| chr11:111688237
|
G | A | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0026g0104 | 3 | HG00733.hp2 HG01099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.478+75G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111688237 | ||||||
| chr11:111688574
|
G | A | 5 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+412G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111688574 | ||||||
| chr11:111688792
|
T | G | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478+630T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111688792 | ||||||
| chr11:111688959
|
G | A | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.478+797G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111688959 | ||||||
| chr11:111689062
|
T | C | 1 | a0001c0001t0018g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.478+900T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689062 | ||||||
| chr11:111689225
|
T | C | 4 | a0001c0001t0001g0049a0001c0001t0012g0035a0001c0001t0029g0097others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1063T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689225 | ||||||
| chr11:111689304
|
G | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0019others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.478+1142G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689304 | ||||||
| chr11:111689332
|
A | C | 2 | a0001c0001t0003g0165a0001c0001t0033g0174 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.478+1170A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689332 | ||||||
| chr11:111689722
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478+1560G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689722 | ||||||
| chr11:111689970
|
G | A | 1 | a0001c0001t0041g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.478+1808G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111689970 | ||||||
| chr11:111689984
|
GTA | G | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0180others(89): Show | 92 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.478+1838_478+1839d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111689984 | |||||
| chr11:111690091
|
T | C | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.478+1929T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690091 | ||||||
| chr11:111690169
|
C | A | 1 | a0001c0001t0036g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.478+2007C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690169 | ||||||
| chr11:111690235
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.478+2073G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690235 | ||||||
| chr11:111690272
|
C | CT | 12 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.478+2127dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111690272 | |||||
| chr11:111690272
|
CT | C | 56 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.478+2127delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111690272 | |||||
| chr11:111690372
|
A | G | 6 | a0001c0001t0001g0093a0001c0001t0012g0031a0001c0001t0012g0032others(3): Show | 6 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+2210A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690372 | ||||||
| chr11:111690682
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.478+2520A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690682 | ||||||
| chr11:111690922
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.478+2760A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111690922 | ||||||
| chr11:111691144
|
G | A | 1 | a0001c0006t0025g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.478+2982G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691144 | ||||||
| chr11:111691268
|
A | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.478+3106A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691268 | ||||||
| chr11:111691372
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478+3210A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691372 | ||||||
| chr11:111691383
|
A | C | 2 | a0001c0001t0001g0105a0001c0001t0039g0143 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.478+3221A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691383 | ||||||
| chr11:111691499
|
C | T | 1 | a0001c0001t0002g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.478+3337C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691499 | ||||||
| chr11:111691924
|
G | C | 1 | a0001c0001t0003g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.478+3762G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691924 | ||||||
| chr11:111691968
|
T | A | 44 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(41): Show | 44 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.478+3806T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691968 | ||||||
| chr11:111691984
|
G | A | 2 | a0001c0001t0022g0008a0001c0001t0022g0050 | 2 | HG02056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.478+3822G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111691984 | ||||||
| chr11:111692350
|
C | CA | 8 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0005g0137others(5): Show | 8 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.478+4226dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAA | 7 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0182others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+4222_478+4226d others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAA | 10 | a0001c0001t0003g0125a0001c0001t0003g0159a0001c0001t0003g0163others(7): Show | 10 | HG01070.hp2 HG01516.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.478+4221_478+4226d others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA | 5 | a0001c0001t0005g0130a0001c0001t0011g0124a0001c0001t0051g0153others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+4220_478+4226d others(9): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0172a0001c0001t0008g0175 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.478+4216_478+4226d others(13): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0180a0001c0001t0009g0122a0001c0001t0009g0164others(1): Show | 4 | HG01891.hp2 HG02129.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+4215_478+4226d others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0013g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.478+4214_478+4226d others(15): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0003g0173a0001c0001t0009g0166 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.478+4210_478+4226d others(19): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.478+4207_478+4226d others(22): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0008g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478+4202_478+4226d others(27): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0008g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.478+4201_478+4226d others(28): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CA | C | 7 | a0001c0001t0006g0084a0001c0001t0006g0085a0001c0001t0006g0086others(4): Show | 7 | HG00558.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+4226delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAA | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0002g0014others(7): Show | 10 | HG00621.hp2 HG00642.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+4224_478+4226d others(5): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAA | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0023others(16): Show | 19 | HG00621.hp1 HG00738.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.478+4223_478+4226d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAA | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(27): Show | 30 | HG01169.hp1 HG01255.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.478+4222_478+4226d others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAA | C | 27 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0040others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.478+4221_478+4226d others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0003g0181others(2): Show | 5 | HG00558.hp2 HG01243.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+4220_478+4226d others(9): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0004g0158a0001c0001t0014g0116a0001c0001t0014g0117others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+4217_478+4226d others(12): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0004g0157a0001c0001t0033g0174a0001c0001t0053g0118 | 3 | HG02970.hp1 HG03579.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.478+4216_478+4226d others(13): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0004g0107others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+4213_478+4226d others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(8): Show |
C | 10 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+4212_478+4226d others(17): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0015g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478+4211_478+4226d others(18): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0015g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.478+4210_478+4226d others(19): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0008g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.478+4208_478+4226d others(21): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(13): Show |
C | 4 | a0001c0001t0001g0072a0001c0001t0011g0026a0001c0001t0041g0073others(1): Show | 4 | HG00733.hp1 HG02451.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+4207_478+4226d others(22): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(14): Show |
C | 5 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(2): Show | 5 | HG01952.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+4206_478+4226d others(23): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692350
|
CAAAAAAA others(18): Show |
C | 2 | a0001c0001t0001g0096a0001c0001t0036g0065 | 2 | HG00140.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.478+4202_478+4226d others(27): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111692350 | |||||
| chr11:111692387
|
A | AC | 2 | a0001c0001t0018g0140a0001c0001t0047g0001 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.478+4225_478+4226i others(3): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111692387 | ||||||
| chr11:111692694
|
T | A | 1 | a0001c0001t0002g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.478+4532T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111692694 | ||||||
| chr11:111692927
|
T | G | 1 | a0001c0001t0017g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.478+4765T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111692927 | ||||||
| chr11:111693032
|
G | A | 1 | a0001c0007t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478+4870G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693032 | ||||||
| chr11:111693104
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.478+4942T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693104 | ||||||
| chr11:111693109
|
G | A | 1 | a0001c0001t0049g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478+4947G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693109 | ||||||
| chr11:111693291
|
G | A | 1 | a0001c0001t0001g0003 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478+5129G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693291 | ||||||
| chr11:111693604
|
A | G | 2 | a0001c0001t0007g0109a0001c0001t0007g0115 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.478+5442A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693604 | ||||||
| chr11:111693945
|
A | G | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478+5783A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111693945 | ||||||
| chr11:111694542
|
T | C | 5 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-6344T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111694542 | ||||||
| chr11:111694810
|
T | C | 1 | a0001c0001t0002g0017 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.479-6076T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111694810 | ||||||
| chr11:111694851
|
A | T | 2 | a0001c0002t0003g0193a0001c0002t0034g0194 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.479-6035A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111694851 | ||||||
| chr11:111694981
|
A | C | 1 | a0001c0001t0059g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.479-5905A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111694981 | ||||||
| chr11:111695021
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.479-5865G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111695021 | ||||||
| chr11:111695447
|
G | A | 15 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(12): Show | 15 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.479-5439G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111695447 | ||||||
| chr11:111695547
|
T | C | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.479-5339T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111695547 | ||||||
| chr11:111696341
|
T | G | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.479-4545T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111696341 | ||||||
| chr11:111697038
|
A | G | 1 | a0001c0001t0008g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.479-3848A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697038 | ||||||
| chr11:111697367
|
G | A | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.479-3519G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697367 | ||||||
| chr11:111697714
|
G | C | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.479-3172G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697714 | ||||||
| chr11:111697753
|
T | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.479-3133T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697753 | ||||||
| chr11:111697837
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.479-3049G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697837 | ||||||
| chr11:111697845
|
A | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.479-3041A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697845 | ||||||
| chr11:111697957
|
C | T | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.479-2929C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111697957 | ||||||
| chr11:111698262
|
G | A | 2 | a0001c0001t0018g0140a0002c0005t0018g0101 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.479-2624G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698262 | ||||||
| chr11:111698297
|
G | A | 5 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(2): Show | 5 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-2589G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698297 | ||||||
| chr11:111698462
|
G | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0069 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.479-2424G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698462 | ||||||
| chr11:111698523
|
C | T | 2 | a0001c0001t0020g0133a0001c0001t0020g0134 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.479-2363C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698523 | ||||||
| chr11:111698533
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.479-2353G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698533 | ||||||
| chr11:111698562
|
C | T | 2 | a0001c0001t0037g0120a0001c0001t0047g0001 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.479-2324C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698562 | ||||||
| chr11:111698643
|
G | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.479-2243G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111698643 | ||||||
| chr11:111699019
|
T | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.479-1867T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699019 | ||||||
| chr11:111699207
|
G | A | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.479-1679G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699207 | ||||||
| chr11:111699275
|
T | G | 2 | a0001c0001t0010g0079a0001c0001t0010g0081 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.479-1611T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699275 | ||||||
| chr11:111699318
|
T | C | 1 | a0001c0001t0005g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.479-1568T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699318 | ||||||
| chr11:111699415
|
G | A | 1 | a0001c0001t0012g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.479-1471G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699415 | ||||||
| chr11:111699631
|
T | C | 2 | a0001c0001t0037g0120a0001c0001t0047g0001 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.479-1255T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699631 | ||||||
| chr11:111699806
|
A | G | 1 | a0001c0001t0037g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.479-1080A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111699806 | ||||||
| chr11:111700089
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.479-797G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111700089 | ||||||
| chr11:111700119
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.479-767C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111700119 | ||||||
| chr11:111700396
|
G | GA | 8 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.479-487dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 111700396 | |||||
| chr11:111700416
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0007g0108others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.479-470C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111700416 | ||||||
| chr11:111700472
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.479-414G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111700472 | ||||||
| chr11:111700498
|
T | A | 1 | a0001c0001t0012g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.479-388T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 4/14 | chr11 | 111700498 | ||||||
| chr11:111701924
|
T | A | 1 | a0001c0001t0059g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.727+349T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111701924 | ||||||
| chr11:111702215
|
A | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.727+640A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702215 | ||||||
| chr11:111702445
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.728-758C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702445 | ||||||
| chr11:111702510
|
A | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0055others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-693A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702510 | ||||||
| chr11:111702629
|
A | G | 23 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.728-574A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702629 | ||||||
| chr11:111702676
|
G | A | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-527G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702676 | ||||||
| chr11:111702686
|
T | C | 5 | a0001c0001t0001g0105a0001c0001t0039g0143a0001c0001t0056g0146others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-517T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702686 | ||||||
| chr11:111702727
|
G | A | 1 | a0001c0001t0015g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728-476G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702727 | ||||||
| chr11:111702860
|
A | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.728-343A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | chr11 | 111702860 | ||||||
| chr11:111702925
|
C | CTGTT | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.728-276_728-273dup others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 111702925 | |||||
| chr11:111703990
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.948+567C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | chr11 | 111703990 | ||||||
| chr11:111704072
|
C | T | 1 | a0001c0001t0063g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.948+649C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | chr11 | 111704072 | ||||||
| chr11:111704357
|
C | T | 11 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(8): Show | 11 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.949-630C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | chr11 | 111704357 | ||||||
| chr11:111704471
|
G | A | 12 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(9): Show | 12 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.949-516G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | chr11 | 111704471 | ||||||
| chr11:111704910
|
C | CT | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.949-68dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 111704910 | |||||
| chr11:111704925
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0044 | 2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.949-62T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 7/14 | chr11 | 111704925 | ||||||
| chr11:111705259
|
T | A | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101+120T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111705259 | ||||||
| chr11:111705434
|
C | T | 42 | a0001c0001t0002g0180a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1101+295C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111705434 | ||||||
| chr11:111705638
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1101+499C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111705638 | ||||||
| chr11:111705870
|
G | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1101+731G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111705870 | ||||||
| chr11:111706074
|
T | C | 2 | a0001c0001t0060g0102a0001c0001t0061g0103 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1101+935T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111706074 | ||||||
| chr11:111706095
|
G | A | 2 | a0001c0001t0005g0129a0001c0001t0005g0139 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1101+956G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111706095 | ||||||
| chr11:111706452
|
G | T | 1 | a0001c0001t0062g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1101+1313G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111706452 | ||||||
| chr11:111706900
|
A | C | 3 | a0001c0001t0014g0116a0001c0001t0014g0117a0001c0001t0052g0005 | 3 | HG00733.hp2 HG01099.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1101+1761A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111706900 | ||||||
| chr11:111706916
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1101+1777C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111706916 | ||||||
| chr11:111706959
|
CA | C | 5 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0005g0127others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+1841delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 111706959 | |||||
| chr11:111706959
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0040g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1101+1831_1101+184 others(15): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 111706959 | |||||
| chr11:111707398
|
TA | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1101+2262delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 111707398 | |||||
| chr11:111707492
|
G | C | 1 | a0001c0001t0056g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1101+2353G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111707492 | ||||||
| chr11:111707533
|
TC | T | 2 | a0001c0001t0002g0024a0001c0001t0046g0052 | 2 | NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1101+2395delC | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111707533 | ||||||
| chr11:111707589
|
C | T | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1101+2450C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111707589 | ||||||
| chr11:111708132
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0007g0108a0001c0001t0007g0109others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1101+2993G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708132 | ||||||
| chr11:111708165
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1101+3026T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708165 | ||||||
| chr11:111708198
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1101+3059A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708198 | ||||||
| chr11:111708377
|
G | A | 1 | a0001c0001t0047g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1101+3238G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708377 | ||||||
| chr11:111708385
|
A | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.1101+3246A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708385 | ||||||
| chr11:111708451
|
C | A | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+3312C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111708451 | ||||||
| chr11:111709002
|
T | G | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1102-3209T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709002 | ||||||
| chr11:111709131
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1102-3080G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709131 | ||||||
| chr11:111709146
|
G | A | 2 | a0001c0001t0007g0109a0001c0001t0007g0115 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1102-3065G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709146 | ||||||
| chr11:111709215
|
G | C | 43 | a0001c0001t0002g0180a0001c0001t0003g0054a0001c0001t0003g0125others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1102-2996G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709215 | ||||||
| chr11:111709305
|
A | G | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1102-2906A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709305 | ||||||
| chr11:111709458
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1102-2753G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709458 | ||||||
| chr11:111709520
|
A | C | 1 | a0001c0001t0002g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1102-2691A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709520 | ||||||
| chr11:111709657
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1102-2554A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111709657 | ||||||
| chr11:111710284
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1102-1927A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710284 | ||||||
| chr11:111710419
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1102-1792A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710419 | ||||||
| chr11:111710422
|
T | C | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1102-1789T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710422 | ||||||
| chr11:111710445
|
T | C | 1 | a0001c0001t0053g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1102-1766T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710445 | ||||||
| chr11:111710604
|
T | C | 1 | a0001c0001t0028g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1102-1607T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710604 | ||||||
| chr11:111710797
|
C | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1102-1414C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111710797 | ||||||
| chr11:111711042
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1102-1169G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711042 | ||||||
| chr11:111711121
|
A | AT | 16 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0051others(13): Show | 16 | HG00733.hp2 HG01099.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1102-1075dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 111711121 | |||||
| chr11:111711182
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1102-1029G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711182 | ||||||
| chr11:111711253
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0039g0143a0001c0001t0056g0146others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-958G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711253 | ||||||
| chr11:111711329
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0029g0097a0001c0001t0046g0052 | 3 | HG01192.hp2 HG01978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1102-882G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711329 | ||||||
| chr11:111711558
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1102-653G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711558 | ||||||
| chr11:111711721
|
T | C | 8 | a0001c0001t0005g0129a0001c0001t0005g0130a0001c0001t0005g0132others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-490T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711721 | ||||||
| chr11:111711734
|
C | T | 2 | a0001c0001t0047g0001a0001c0001t0063g0192 | 2 | HG00558.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1102-477C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711734 | ||||||
| chr11:111711771
|
G | A | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1102-440G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 8/14 | chr11 | 111711771 | ||||||
| chr11:111712475
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1266+100C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712475 | ||||||
| chr11:111712535
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1266+160C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712535 | ||||||
| chr11:111712853
|
A | G | 2 | a0001c0001t0004g0152a0001c0001t0004g0158 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1266+478A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712853 | ||||||
| chr11:111712884
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+509G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712884 | ||||||
| chr11:111712885
|
C | G | 3 | a0001c0001t0001g0093a0001c0001t0008g0039a0001c0001t0008g0046 | 3 | HG01109.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1266+510C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712885 | ||||||
| chr11:111712992
|
C | T | 12 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(9): Show | 12 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+617C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111712992 | ||||||
| chr11:111713097
|
C | T | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1266+722C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713097 | ||||||
| chr11:111713192
|
AAGTT | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0019others(33): Show | 36 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1266+821_1266+824d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111713192 | |||||
| chr11:111713233
|
G | T | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+858G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713233 | ||||||
| chr11:111713343
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1266+968A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713343 | ||||||
| chr11:111713446
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0039g0143 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1266+1071G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713446 | ||||||
| chr11:111713649
|
C | T | 1 | a0001c0001t0006g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1266+1274C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713649 | ||||||
| chr11:111713772
|
G | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+1397G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111713772 | ||||||
| chr11:111714179
|
G | C | 10 | a0001c0001t0001g0106a0001c0001t0007g0108a0001c0001t0007g0109others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1266+1804G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714179 | ||||||
| chr11:111714446
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1266+2071A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714446 | ||||||
| chr11:111714472
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+2097T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714472 | ||||||
| chr11:111714522
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+2147G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714522 | ||||||
| chr11:111714541
|
T | G | 1 | a0001c0003t0003g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1266+2166T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714541 | ||||||
| chr11:111714812
|
G | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+2437G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714812 | ||||||
| chr11:111714846
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+2471T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111714846 | ||||||
| chr11:111715149
|
C | T | 10 | a0001c0001t0001g0106a0001c0001t0007g0108a0001c0001t0007g0109others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1266+2774C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715149 | ||||||
| chr11:111715174
|
C | T | 2 | a0001c0001t0023g0015a0001c0001t0023g0016 | 2 | HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1266+2799C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715174 | ||||||
| chr11:111715195
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+2820T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715195 | ||||||
| chr11:111715281
|
C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1266+2906C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715281 | ||||||
| chr11:111715307
|
G | GCA | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1266+2945_1266+294 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111715307 | |||||
| chr11:111715367
|
C | G | 42 | a0001c0001t0003g0054a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1266+2992C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715367 | ||||||
| chr11:111715418
|
T | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1266+3043T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715418 | ||||||
| chr11:111715607
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+3232T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715607 | ||||||
| chr11:111715682
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+3307A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715682 | ||||||
| chr11:111715695
|
G | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+3320G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715695 | ||||||
| chr11:111715754
|
A | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1266+3379A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111715754 | ||||||
| chr11:111715793
|
C | CT | 49 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0067others(46): Show | 49 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1266+3443dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111715793 | |||||
| chr11:111715793
|
C | CTT | 6 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0004g0158others(3): Show | 6 | HG01255.hp2 HG02293.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+3442_1266+344 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111715793 | |||||
| chr11:111715793
|
CT | C | 7 | a0001c0001t0001g0105a0001c0001t0003g0165a0001c0001t0009g0170others(4): Show | 7 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1266+3443delT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111715793 | |||||
| chr11:111715793
|
CTT | C | 37 | a0001c0001t0003g0054a0001c0001t0003g0125a0001c0001t0003g0159others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1266+3442_1266+344 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111715793 | |||||
| chr11:111716022
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1266+3647G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716022 | ||||||
| chr11:111716226
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1267-3549G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716226 | ||||||
| chr11:111716237
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1267-3538C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716237 | ||||||
| chr11:111716414
|
T | TA | 42 | a0001c0001t0003g0054a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1267-3356dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111716414 | |||||
| chr11:111716449
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-3326T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716449 | ||||||
| chr11:111716491
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-3284T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716491 | ||||||
| chr11:111716579
|
CAAAAAAA | C | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG01109.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1267-3195_1267-318 others(11): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716579 | ||||||
| chr11:111716587
|
G | C | 1 | a0001c0002t0003g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1267-3188G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716587 | ||||||
| chr11:111716771
|
G | A | 42 | a0001c0001t0003g0054a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1267-3004G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716771 | ||||||
| chr11:111716906
|
C | T | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-2869C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111716906 | ||||||
| chr11:111717132
|
G | T | 1 | a0001c0001t0008g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1267-2643G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717132 | ||||||
| chr11:111717177
|
G | T | 42 | a0001c0001t0003g0054a0001c0001t0003g0125a0001c0001t0003g0159others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1267-2598G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717177 | ||||||
| chr11:111717197
|
T | A | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-2578T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717197 | ||||||
| chr11:111717241
|
G | T | 8 | a0001c0001t0010g0077a0001c0001t0010g0078a0001c0001t0010g0079others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-2534G>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717241 | ||||||
| chr11:111717282
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1267-2493C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717282 | ||||||
| chr11:111717317
|
C | CA | 41 | a0001c0001t0002g0038a0001c0001t0002g0068a0001c0001t0003g0125others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1267-2432dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAA | 73 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1267-2433_1267-243 others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAAA | 32 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0036others(29): Show | 32 | HG00621.hp1 HG00621.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1267-2434_1267-243 others(7): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAAAA | 7 | a0001c0001t0002g0196a0001c0001t0006g0090a0001c0001t0015g0099others(4): Show | 7 | HG02109.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-2435_1267-243 others(8): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAAAAA | 7 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0105others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-2436_1267-243 others(9): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0014g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1267-2441_1267-243 others(14): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0014g0117 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1267-2443_1267-243 others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
CA | C | 13 | a0001c0001t0005g0126a0001c0001t0005g0127a0001c0001t0005g0129others(10): Show | 13 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267-2432delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
CAAAAAAA | C | 14 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(11): Show | 14 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1267-2438_1267-243 others(11): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717317
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0003g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1267-2443_1267-243 others(16): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111717317 | |||||
| chr11:111717528
|
G | A | 1 | a0001c0001t0013g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1267-2247G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717528 | ||||||
| chr11:111717600
|
C | G | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-2175C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717600 | ||||||
| chr11:111717664
|
T | A | 1 | a0001c0001t0001g0002 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1267-2111T>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717664 | ||||||
| chr11:111717755
|
T | C | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1267-2020T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717755 | ||||||
| chr11:111717760
|
A | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-2015A>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717760 | ||||||
| chr11:111717951
|
T | C | 2 | a0001c0001t0005g0126a0001c0001t0005g0127 | 2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1267-1824T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111717951 | ||||||
| chr11:111718013
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0057 | 3 | HG00558.hp2 HG02135.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1267-1762G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718013 | ||||||
| chr11:111718148
|
G | C | 1 | a0001c0001t0010g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1267-1627G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718148 | ||||||
| chr11:111718190
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1267-1585C>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718190 | ||||||
| chr11:111718311
|
G | A | 2 | a0001c0001t0007g0109a0001c0001t0007g0115 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1267-1464G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718311 | ||||||
| chr11:111718476
|
G | A | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1267-1299G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718476 | ||||||
| chr11:111718482
|
C | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0038 | 3 | HG01496.hp2 HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1267-1293C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718482 | ||||||
| chr11:111718762
|
T | C | 2 | a0001c0001t0016g0075a0001c0001t0016g0076 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1267-1013T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718762 | ||||||
| chr11:111718831
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0007g0108a0001c0001t0007g0109others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1267-944G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718831 | ||||||
| chr11:111718889
|
G | A | 1 | a0001c0001t0026g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1267-886G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718889 | ||||||
| chr11:111718936
|
T | G | 1 | a0001c0001t0052g0005 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1267-839T>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718936 | ||||||
| chr11:111718941
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1267-834T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718941 | ||||||
| chr11:111718997
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0041g0073a0001c0001t0048g0071 | 3 | HG00733.hp1 HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1267-778C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111718997 | ||||||
| chr11:111719177
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1267-598A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719177 | ||||||
| chr11:111719340
|
A | T | 23 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1267-435A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719340 | ||||||
| chr11:111719356
|
CTT | C | 13 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0196others(10): Show | 13 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267-401_1267-400d others(4): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111719356 | |||||
| chr11:111719356
|
CTTT | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1267-402_1267-400d others(5): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111719356 | |||||
| chr11:111719356
|
CTTTT | C | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG00733.hp2 HG01099.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267-403_1267-400d others(6): Show |
SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111719356 | |||||
| chr11:111719357
|
T | C | 3 | a0001c0001t0030g0121a0001c0001t0054g0141a0001c0001t0055g0142 | 3 | HG02486.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1267-418T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719357 | ||||||
| chr11:111719359
|
T | C | 1 | a0001c0001t0060g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1267-416T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719359 | ||||||
| chr11:111719360
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1267-415T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719360 | ||||||
| chr11:111719388
|
A | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1267-387A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719388 | ||||||
| chr11:111719394
|
T | TA | 6 | a0001c0001t0001g0013a0001c0001t0001g0093a0001c0001t0008g0039others(3): Show | 6 | HG01109.hp1 HG01255.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-368dupA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111719394 | |||||
| chr11:111719394
|
TA | T | 5 | a0001c0001t0006g0087a0001c0001t0014g0116a0001c0001t0014g0117others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1267-368delA | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 111719394 | |||||
| chr11:111719408
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1267-367C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719408 | ||||||
| chr11:111719448
|
A | T | 1 | a0001c0001t0062g0018 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1267-327A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719448 | ||||||
| chr11:111719480
|
C | A | 1 | a0001c0004t0042g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1267-295C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 9/14 | chr11 | 111719480 | ||||||
| chr11:111720131
|
A | T | 1 | a0001c0001t0006g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1495+128A>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 10/14 | chr11 | 111720131 | ||||||
| chr11:111720216
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0069 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1495+213G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 10/14 | chr11 | 111720216 | ||||||
| chr11:111720330
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1496-148T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 10/14 | chr11 | 111720330 | ||||||
| chr11:111720866
|
G | C | 1 | a0001c0001t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1781-33G>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 11/14 | chr11 | 111720866 | ||||||
| chr11:111720874
|
G | A | 1 | a0001c0004t0042g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1781-25G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 11/14 | chr11 | 111720874 | ||||||
| chr11:111721263
|
A | G | 13 | a0001c0001t0004g0107a0001c0001t0004g0147a0001c0001t0004g0148others(10): Show | 13 | HG01952.hp2 HG02723.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1944+201A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/14 | chr11 | 111721263 | ||||||
| chr11:111721393
|
C | A | 5 | a0001c0001t0009g0122a0001c0001t0009g0164a0001c0001t0009g0166others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944+331C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/14 | chr11 | 111721393 | ||||||
| chr11:111721602
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1945-228T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/14 | chr11 | 111721602 | ||||||
| chr11:111721747
|
C | A | 1 | a0001c0001t0041g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1945-83C>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/14 | chr11 | 111721747 | ||||||
| chr11:111721780
|
G | A | 1 | a0002c0005t0018g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1945-50G>A | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 12/14 | chr11 | 111721780 | ||||||
| chr11:111722152
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2055+212A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 13/14 | chr11 | 111722152 | ||||||
| chr11:111722467
|
G | GT | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2056-197dupT | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 111722467 | |||||
| chr11:111722990
|
T | C | 2 | a0001c0001t0014g0116a0001c0001t0014g0117 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2147+234T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 14/14 | chr11 | 111722990 | ||||||
| chr11:111723255
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2148-241C>T | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 14/14 | chr11 | 111723255 | ||||||
| chr11:111723340
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2148-156A>G | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 14/14 | chr11 | 111723340 | ||||||
| chr11:111723353
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.2148-143T>C | SIK2 | ENSG00000170145.5 | transcript | ENST00000304987.4 | protein_coding | 14/14 | chr11 | 111723353 |