Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6789 |
|---|---|
| ensemblid | ENSG00000101109.13 |
| hgncid | 11408 |
| symbol | STK4 |
| name | serine/threonine kinase 4 |
| refseq_nuc | NM_006282.5 |
| refseq_prot | NP_006273.1 |
| ensembl_nuc | ENST00000372806.8 |
| ensembl_prot | ENSP00000361892.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 44966512 |
| end | 45080021 |
| strand | + |
| ver | v1.2 |
| region | chr20:44966512-45080021 |
| region5000 | chr20:44961512-45085021 |
| regionname0 | STK4_chr20_44966512_45080021 |
| regionname5000 | STK4_chr20_44961512_45085021 |
| 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 | 1/0 | 487 | 275 | 77 | 35 | 130 | 5 | 27 | 104 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002 | 0/1 | 487 | 47 | 12 | 13 | 1 | 9 | 11 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0003 | 0/0 | 487 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0004 | 0/0 | 487 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0005 | 0/0 | 487 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1464 | 275 | 77 | 35 | 130 | 5 | 27 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| c0002 | 0/1 | 1464 | 46 | 11 | 13 | 1 | 9 | 11 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| c0003 | 0/0 | 1464 | 4 | 0 | 0 | 4 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| c0004 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| c0005 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| c0006 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4903 | 94 | 13 | 14 | 48 | 3 | 15 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0002 | 0/0 | 4901 | 38 | 0 | 4 | 27 | 1 | 6 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0003 | 0/0 | 4903 | 32 | 11 | 7 | 0 | 7 | 7 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0004 | 0/0 | 4904 | 28 | 0 | 6 | 18 | 0 | 4 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0005 | 0/0 | 4905 | 28 | 24 | 4 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0006 | 0/0 | 4903 | 13 | 0 | 0 | 13 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0007 | 0/1 | 4904 | 13 | 1 | 4 | 1 | 2 | 4 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0008 | 0/0 | 4902 | 9 | 8 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0009 | 0/0 | 4903 | 8 | 0 | 0 | 8 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0010 | 0/0 | 4904 | 7 | 0 | 0 | 6 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0011 | 0/0 | 4902 | 7 | 5 | 2 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0012 | 0/0 | 4904 | 6 | 4 | 1 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0013 | 0/0 | 4903 | 4 | 4 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0014 | 0/0 | 4903 | 3 | 3 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0015 | 0/0 | 4902 | 3 | 0 | 0 | 3 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0016 | 0/0 | 4904 | 2 | 1 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0017 | 0/0 | 4903 | 2 | 0 | 0 | 2 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0018 | 0/0 | 4904 | 2 | 2 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0019 | 0/0 | 4903 | 2 | 2 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0020 | 0/0 | 4904 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0021 | 0/0 | 4905 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0022 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0023 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0024 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0025 | 0/0 | 4903 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0026 | 0/0 | 4902 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0027 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0028 | 0/0 | 4899 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0029 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0030 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0031 | 0/0 | 4903 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0032 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0033 | 0/0 | 4902 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0034 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0035 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0036 | 0/0 | 4904 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0037 | 0/0 | 4903 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0038 | 0/0 | 4902 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0039 | 0/0 | 4902 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0040 | 0/0 | 4901 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0041 | 0/0 | 4901 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0042 | 0/0 | 4902 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0043 | 0/0 | 4902 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0044 | 0/0 | 4902 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0045 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| t0046 | 0/0 | 4905 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1464 | 275 | 77 | 35 | 130 | 5 | 27 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002 | 0/1 | 1464 | 46 | 11 | 13 | 1 | 9 | 11 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0005 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0003c0003 | 0/0 | 1464 | 4 | 0 | 0 | 4 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0004c0004 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0005c0006 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6366 | 90 | 13 | 14 | 44 | 3 | 15 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0002 | 0/0 | 6364 | 38 | 0 | 4 | 27 | 1 | 6 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0003 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0004 | 0/0 | 6367 | 28 | 0 | 6 | 18 | 0 | 4 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0005 | 0/0 | 6368 | 28 | 24 | 4 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0006 | 0/0 | 6366 | 13 | 0 | 0 | 13 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0008 | 0/0 | 6365 | 9 | 8 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0009 | 0/0 | 6366 | 8 | 0 | 0 | 8 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0010 | 0/0 | 6367 | 7 | 0 | 0 | 6 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0011 | 0/0 | 6365 | 6 | 5 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0012 | 0/0 | 6367 | 6 | 4 | 1 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0013 | 0/0 | 6366 | 3 | 3 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0014 | 0/0 | 6366 | 3 | 3 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0015 | 0/0 | 6365 | 3 | 0 | 0 | 3 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0016 | 0/0 | 6367 | 2 | 1 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0017 | 0/0 | 6366 | 2 | 0 | 0 | 2 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0018 | 0/0 | 6367 | 2 | 2 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0019 | 0/0 | 6366 | 2 | 2 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0020 | 0/0 | 6367 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0021 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0022 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0023 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0024 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0025 | 0/0 | 6366 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0026 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0027 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0028 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0029 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0030 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0031 | 0/0 | 6366 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0032 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0033 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0034 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0035 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0037 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0038 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0039 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0040 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0041 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0042 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0044 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0001c0001t0046 | 0/0 | 6368 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002t0003 | 0/0 | 6366 | 30 | 9 | 7 | 0 | 7 | 7 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002t0007 | 0/1 | 6367 | 13 | 1 | 4 | 1 | 2 | 4 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002t0011 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002t0036 | 0/0 | 6367 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0002t0043 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0002c0005t0003 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0003c0003t0001 | 0/0 | 6366 | 3 | 0 | 0 | 3 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0003c0003t0045 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0004c0004t0001 | 0/0 | 6366 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| a0005c0006t0013 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | copy fasta | chr20 | 44961512 | 45085021 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0014g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0015g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0017g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0019g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0020g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0021g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0022g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0023g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0024g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0025g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0026g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0027g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0028g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0029g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0030g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0031g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0032g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0033g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0034g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0035g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0037g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0038g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0039g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0040g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0041g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0042g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0044g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0001c0001t0046g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0036g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0002t0043g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0002c0005t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0003c0003t0045g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| a0005c0006t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00099 | hp2 | a0002 | c0002 | t0007 | g0141 | EUR | GBR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0147 | EUR | FIN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00280 | hp2 | a0001 | c0001 | t0026 | g0274 | EUR | FIN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0161 | EUR | FIN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00323 | hp2 | a0002 | c0002 | t0003 | g0160 | EUR | FIN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00597 | hp2 | a0001 | c0001 | t0017 | g0031 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00621 | hp1 | a0001 | c0001 | t0009 | g0209 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | CHS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00639 | hp1 | a0001 | c0001 | t0020 | g0260 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00639 | hp2 | a0002 | c0002 | t0036 | g0167 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00735 | hp1 | a0001 | c0001 | t0033 | g0083 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0157 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00738 | hp2 | a0002 | c0002 | t0007 | g0165 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0154 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01081 | hp1 | a0001 | c0001 | t0012 | g0044 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01167 | hp1 | a0001 | c0001 | t0046 | g0079 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01167 | hp2 | a0001 | c0001 | t0025 | g0226 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01168 | hp2 | a0002 | c0002 | t0007 | g0140 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0180 | AMR | PUR | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0138 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0146 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0224 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0152 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0143 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01358 | hp1 | a0002 | c0002 | t0007 | g0158 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0085 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | IBS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0139 | EUR | IBS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01517 | hp1 | a0002 | c0002 | t0007 | g0169 | EUR | IBS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0166 | EUR | IBS | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01884 | hp1 | a0001 | c0001 | t0037 | g0222 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01891 | hp1 | a0001 | c0001 | t0044 | g0176 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0219 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0046 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02040 | hp2 | a0003 | c0003 | t0045 | g0305 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0038 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02074 | hp2 | a0001 | c0001 | t0015 | g0122 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02135 | hp2 | a0001 | c0001 | t0041 | g0120 | EAS | KHV | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02145 | hp1 | a0002 | c0005 | t0003 | g0170 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0225 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0279 | EAS | CDX | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CDX | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02165 | hp1 | a0001 | c0001 | t0040 | g0107 | EAS | CDX | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0153 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0183 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02300 | hp2 | a0002 | c0002 | t0011 | g0078 | AMR | PEL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02572 | hp1 | a0005 | c0006 | t0013 | g0216 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0215 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0229 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0070 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0212 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0257 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0185 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02683 | hp2 | a0001 | c0001 | t0031 | g0301 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0211 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02723 | hp1 | a0002 | c0002 | t0043 | g0084 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02735 | hp1 | a0002 | c0002 | t0007 | g0164 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0177 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0142 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0133 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0049 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0052 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0053 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0256 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02965 | hp1 | a0001 | c0001 | t0039 | g0127 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0086 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0218 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0178 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0223 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0272 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03041 | hp1 | a0001 | c0001 | t0035 | g0045 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03098 | hp2 | a0001 | c0001 | t0038 | g0220 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0258 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0050 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03239 | hp2 | a0002 | c0002 | t0007 | g0162 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0144 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0323 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0181 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | ESN | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0182 | AFR | GWD | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0134 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03669 | hp1 | a0002 | c0002 | t0007 | g0159 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03688 | hp2 | a0002 | c0002 | t0007 | g0136 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0135 | SAS | PJL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0155 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | BEB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0151 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | YRI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0195 | EAS | CHB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18943 | hp2 | a0001 | c0001 | t0024 | g0203 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18946 | hp1 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0210 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0252 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18965 | hp1 | a0001 | c0001 | t0028 | g0268 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18973 | hp2 | a0001 | c0001 | t0009 | g0204 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18974 | hp2 | a0001 | c0001 | t0015 | g0112 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18977 | hp1 | a0001 | c0001 | t0010 | g0254 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18978 | hp1 | a0001 | c0001 | t0016 | g0192 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18980 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18982 | hp2 | a0001 | c0001 | t0022 | g0190 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18989 | hp1 | a0002 | c0002 | t0007 | g0149 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0207 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | LWK | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19030 | hp2 | a0001 | c0001 | t0030 | g0235 | AFR | LWK | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | LWK | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | LWK | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19056 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19057 | hp1 | a0001 | c0001 | t0017 | g0032 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19057 | hp2 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0101 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0242 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0244 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19084 | hp2 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0307 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19088 | hp2 | a0001 | c0001 | t0032 | g0009 | EAS | JPT | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | YRI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | YRI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | ASW | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20129 | hp2 | a0002 | c0002 | t0007 | g0168 | AFR | ASW | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0145 | EUR | TSI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0148 | EUR | TSI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | TSI | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01123 | hp1 | a0002 | c0002 | t0007 | g0163 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | CLM | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0150 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0171 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG02559 | hp2 | a0001 | c0001 | t0042 | g0128 | AFR | ACB | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | MSL | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0173 | AFR | USA | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | USA | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| NA20300 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | USA | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0007 | g0156 | REF | REF | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | STK4_chr20_44961512_45085021 | STK4 | chr20 | 44961512 | 45085021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44981933
|
G | A | 1 | a0004 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.350G>A | p.Arg117Gln | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/11 | 407/6366 | 350/1464 | 117/487 | chr20 | 44981933 | ||
| chr20:45000494
|
G | A | 1 | a0002 | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
missense_variant | MODERATE | c.934G>A | p.Val312Met | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/11 | 991/6366 | 934/1464 | 312/487 | chr20 | 45000494 | ||
| chr20:45001270
|
T | C | 1 | a0003 | 4 | HG02040.hp2 HG02155.hp1 NA18978.hp2 others(1): Show |
missense_variant | MODERATE | c.1064T>C | p.Ile355Thr | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/11 | 1121/6366 | 1064/1464 | 355/487 | chr20 | 45001270 | ||
| chr20:45025046
|
G | T | 1 | a0005 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1221G>T | p.Gln407His | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/11 | 1278/6366 | 1221/1464 | 407/487 | chr20 | 45025046 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:45075056
|
C | T | 1 | a0002c0005 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1344C>T | p.Leu448Leu | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1401/6366 | 1344/1464 | 448/487 | chr20 | 45075056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:45075310
|
G | A | 1 | a0001c0001t0020 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 134 | chr20 | 45075310 | |||||
| chr20:45075404
|
G | A | 1 | a0001c0001t0021 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 228 | chr20 | 45075404 | |||||
| chr20:45075534
|
A | T | 1 | a0001c0001t0009 | 8 | HG00621.hp1 NA18946.hp1 NA18954.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 358 | chr20 | 45075534 | |||||
| chr20:45075546
|
C | CAT | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0046 | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*382_*383dupTA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 384 | INFO_REALIGN_3_PRIME | chr20 | 45075546 | ||||
| chr20:45075638
|
A | G | 1 | a0003c0003t0045 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 462 | chr20 | 45075638 | |||||
| chr20:45075770
|
G | A | 1 | a0001c0001t0022 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*594G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 594 | chr20 | 45075770 | |||||
| chr20:45075946
|
A | G | 2 | a0001c0001t0019a0001c0001t0044 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*770A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 770 | chr20 | 45075946 | |||||
| chr20:45076296
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(19): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1120 | chr20 | 45076296 | |||||
| chr20:45076302
|
T | C | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(30): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1126T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1126 | chr20 | 45076302 | |||||
| chr20:45076312
|
C | T | 1 | a0001c0001t0032 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1136 | chr20 | 45076312 | |||||
| chr20:45076321
|
G | A | 1 | a0001c0001t0033 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1145 | chr20 | 45076321 | |||||
| chr20:45076322
|
C | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(19): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1146C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1146 | chr20 | 45076322 | |||||
| chr20:45076505
|
C | G | 1 | a0002c0002t0043 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1329 | chr20 | 45076505 | |||||
| chr20:45076556
|
G | A | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1380G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1380 | chr20 | 45076556 | |||||
| chr20:45076598
|
C | T | 1 | a0001c0001t0042 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1422C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1422 | chr20 | 45076598 | |||||
| chr20:45076810
|
C | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1634C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1634 | chr20 | 45076810 | |||||
| chr20:45076910
|
C | G | 4 | a0001c0001t0002a0001c0001t0015a0001c0001t0040others(1): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1734C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1734 | chr20 | 45076910 | |||||
| chr20:45077119
|
C | T | 1 | a0001c0001t0044 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1943C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1943 | chr20 | 45077119 | |||||
| chr20:45077139
|
A | G | 1 | a0001c0001t0031 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1963A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 1963 | chr20 | 45077139 | |||||
| chr20:45077283
|
C | T | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2107 | chr20 | 45077283 | |||||
| chr20:45077385
|
G | GTC | 5 | a0001c0001t0003a0002c0002t0003a0002c0002t0007others(2): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2221_*2222dupCT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2223 | INFO_REALIGN_3_PRIME | chr20 | 45077385 | ||||
| chr20:45077412
|
T | G | 1 | a0001c0001t0014 | 3 | HG02647.hp1 HG02922.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2236T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2236 | chr20 | 45077412 | |||||
| chr20:45077433
|
C | T | 3 | a0001c0001t0008a0001c0001t0037a0001c0001t0038 | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2257C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2257 | chr20 | 45077433 | |||||
| chr20:45077554
|
T | G | 1 | a0001c0001t0046 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2378T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2378 | chr20 | 45077554 | |||||
| chr20:45077676
|
C | T | 1 | a0001c0001t0017 | 2 | HG00597.hp2 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2500C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2500 | chr20 | 45077676 | |||||
| chr20:45077760
|
A | T | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2584A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2584 | chr20 | 45077760 | |||||
| chr20:45077787
|
G | A | 1 | a0002c0002t0036 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2611G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2611 | chr20 | 45077787 | |||||
| chr20:45077813
|
C | T | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2637C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2637 | chr20 | 45077813 | |||||
| chr20:45077918
|
G | A | 8 | a0001c0001t0002a0001c0001t0008a0001c0001t0015others(5): Show | 55 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2742G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2742 | chr20 | 45077918 | |||||
| chr20:45077957
|
A | T | 1 | a0001c0001t0038 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2781A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 2781 | chr20 | 45077957 | |||||
| chr20:45078172
|
TA | T | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(19): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*3007delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3007 | INFO_REALIGN_3_PRIME | chr20 | 45078172 | ||||
| chr20:45078172
|
TAA | T | 5 | a0001c0001t0002a0001c0001t0015a0001c0001t0040others(2): Show | 44 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3006_*3007delAA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3006 | INFO_REALIGN_3_PRIME | chr20 | 45078172 | ||||
| chr20:45078208
|
G | GT | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0016others(2): Show | 35 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3047dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3048 | INFO_REALIGN_3_PRIME | chr20 | 45078208 | ||||
| chr20:45078208
|
G | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3032G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3032 | chr20 | 45078208 | |||||
| chr20:45078208
|
GT | G | 5 | a0001c0001t0003a0001c0001t0025a0001c0001t0026others(2): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3047delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3047 | INFO_REALIGN_3_PRIME | chr20 | 45078208 | ||||
| chr20:45078342
|
A | G | 1 | a0001c0001t0041 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3166A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3166 | chr20 | 45078342 | |||||
| chr20:45078479
|
A | G | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3303A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3303 | chr20 | 45078479 | |||||
| chr20:45078567
|
C | CT | 2 | a0001c0001t0012a0001c0001t0018 | 8 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3406dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3407 | INFO_REALIGN_3_PRIME | chr20 | 45078567 | ||||
| chr20:45078582
|
T | C | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3406T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3406 | chr20 | 45078582 | |||||
| chr20:45078605
|
A | G | 1 | a0002c0002t0043 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3429A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3429 | chr20 | 45078605 | |||||
| chr20:45078804
|
C | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3628C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3628 | chr20 | 45078804 | |||||
| chr20:45078843
|
A | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3667A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3667 | chr20 | 45078843 | |||||
| chr20:45078900
|
A | G | 2 | a0001c0001t0018a0001c0001t0035 | 3 | HG02886.hp1 HG03041.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3724A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3724 | chr20 | 45078900 | |||||
| chr20:45079015
|
T | C | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3839T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3839 | chr20 | 45079015 | |||||
| chr20:45079051
|
C | CA | 11 | a0001c0001t0005a0001c0001t0010a0001c0001t0012others(8): Show | 51 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3889dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 3890 | INFO_REALIGN_3_PRIME | chr20 | 45079051 | ||||
| chr20:45079301
|
C | T | 2 | a0001c0001t0014a0001c0001t0030 | 4 | HG02647.hp1 HG02922.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4125C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4125 | chr20 | 45079301 | |||||
| chr20:45079350
|
C | T | 1 | a0001c0001t0029 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4174C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4174 | chr20 | 45079350 | |||||
| chr20:45079512
|
T | G | 1 | a0001c0001t0040 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4336T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4336 | chr20 | 45079512 | |||||
| chr20:45079656
|
T | G | 34 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(31): Show | 183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*4480T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4480 | chr20 | 45079656 | |||||
| chr20:45079818
|
TTGCCCCC others(39): Show |
T | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4644_*4689delGCCC others(42): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4644 | INFO_REALIGN_3_PRIME | chr20 | 45079818 | ||||
| chr20:45079869
|
T | G | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4693T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4693 | chr20 | 45079869 | |||||
| chr20:45079871
|
T | C | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4695T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4695 | chr20 | 45079871 | |||||
| chr20:45079872
|
G | C | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4696G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4696 | chr20 | 45079872 | |||||
| chr20:45079914
|
A | C | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4738A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4738 | chr20 | 45079914 | |||||
| chr20:45079917
|
A | T | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4741A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4741 | chr20 | 45079917 | |||||
| chr20:45079918
|
C | T | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4742C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4742 | chr20 | 45079918 | |||||
| chr20:45079922
|
T | TTTTTTTA others(35): Show |
1 | a0001c0001t0028 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4746_*4747insTTTT others(38): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 11/11 | 4747 | chr20 | 45079922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44967058
|
G | A | 1 | a0001c0001t0005g0002 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.35+455G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967058 | ||||||
| chr20:44967083
|
C | G | 1 | a0001c0001t0002g0327 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.35+480C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967083 | ||||||
| chr20:44967154
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.35+551T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967154 | ||||||
| chr20:44967227
|
T | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00099.hp1 HG00597.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.35+624T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967227 | ||||||
| chr20:44967374
|
T | A | 148 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0174others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.35+771T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967374 | ||||||
| chr20:44967694
|
T | TG | 52 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0179others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.35+1092dupG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44967694 | |||||
| chr20:44967716
|
T | C | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.35+1113T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967716 | ||||||
| chr20:44967851
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.35+1248A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967851 | ||||||
| chr20:44967934
|
G | T | 19 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0322others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.35+1331G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967934 | ||||||
| chr20:44967971
|
G | A | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.35+1368G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44967971 | ||||||
| chr20:44968122
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0042 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.35+1519T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968122 | ||||||
| chr20:44968142
|
C | CT | 47 | a0001c0001t0002g0003a0001c0001t0002g0087a0001c0001t0002g0088others(44): Show | 47 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.35+1552dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44968142 | |||||
| chr20:44968242
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.35+1639A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968242 | ||||||
| chr20:44968320
|
G | A | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.35+1717G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968320 | ||||||
| chr20:44968373
|
G | T | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.35+1770G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968373 | ||||||
| chr20:44968392
|
T | C | 185 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0174others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.35+1789T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968392 | ||||||
| chr20:44968424
|
A | T | 1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.35+1821A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968424 | ||||||
| chr20:44968439
|
G | T | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.35+1836G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968439 | ||||||
| chr20:44968539
|
A | G | 15 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(12): Show | 15 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+1936A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968539 | ||||||
| chr20:44968595
|
G | A | 1 | a0001c0001t0025g0226 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.35+1992G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44968595 | ||||||
| chr20:44969004
|
C | T | 4 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082others(1): Show | 4 | HG01167.hp1 HG01243.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+2401C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969004 | ||||||
| chr20:44969005
|
G | A | 1 | a0001c0001t0006g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.35+2402G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969005 | ||||||
| chr20:44969288
|
C | G | 1 | a0003c0003t0001g0307 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.35+2685C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969288 | ||||||
| chr20:44969391
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.36-2687A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969391 | ||||||
| chr20:44969425
|
G | A | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.36-2653G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969425 | ||||||
| chr20:44969491
|
C | T | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.36-2587C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969491 | ||||||
| chr20:44969513
|
G | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.36-2565G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969513 | ||||||
| chr20:44969525
|
G | GTGAA | 122 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.36-2550_36-2549ins others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44969525 | |||||
| chr20:44969546
|
A | ATCTGTCT others(14): Show |
30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.36-2531_36-2530ins others(21): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44969546 | |||||
| chr20:44969825
|
G | A | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.36-2253G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44969825 | ||||||
| chr20:44970064
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 46 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.36-2014C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970064 | ||||||
| chr20:44970244
|
AAG | A | 6 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(3): Show | 6 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-1832_36-1831del others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44970244 | |||||
| chr20:44970245
|
AG | A | 4 | a0001c0001t0008g0211a0001c0001t0008g0221a0001c0001t0037g0222others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-1832delG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970245 | ||||||
| chr20:44970246
|
GA | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.36-1823delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44970246 | |||||
| chr20:44970255
|
A | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.36-1823A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970255 | ||||||
| chr20:44970502
|
A | G | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-1576A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970502 | ||||||
| chr20:44970527
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.36-1551C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970527 | ||||||
| chr20:44970831
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.36-1247G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970831 | ||||||
| chr20:44970889
|
T | TTG | 102 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0179others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.36-1167_36-1166dup others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44970889 | |||||
| chr20:44970889
|
T | TTGTG | 4 | a0001c0001t0008g0211a0001c0001t0011g0085a0001c0001t0033g0083others(1): Show | 4 | HG00735.hp1 HG01361.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-1169_36-1166dup others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44970889 | |||||
| chr20:44970889
|
TTG | T | 6 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0055others(3): Show | 6 | HG02717.hp1 HG03041.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-1167_36-1166del others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44970889 | |||||
| chr20:44970999
|
T | C | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-1079T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44970999 | ||||||
| chr20:44971017
|
T | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02027.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.36-1061T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971017 | ||||||
| chr20:44971082
|
T | TAC | 52 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0040others(49): Show | 53 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.36-954_36-953dupCA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
T | TACAC | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00099.hp1 HG00597.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.36-956_36-953dupCA others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
T | TACACAC | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(18): Show | 21 | HG01070.hp1 HG02083.hp1 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.36-958_36-953dupCA others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
T | TACACACA others(1): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG02055.hp1 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.36-960_36-953dupCA others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
TAC | T | 50 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0304others(47): Show | 50 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.36-954_36-953delCA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
TACACAC | T | 45 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(42): Show | 45 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.36-958_36-953delCA others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
TACACACA others(1): Show |
T | 21 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0005g0002others(18): Show | 21 | HG01358.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.36-960_36-953delCA others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
TACACACA others(3): Show |
T | 47 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.36-962_36-953delCA others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971082
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.36-964_36-953delCA others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971082 | |||||
| chr20:44971116
|
CACACACA others(3): Show |
C | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.36-960_36-951delCA others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971116 | |||||
| chr20:44971310
|
T | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088 | 3 | HG01074.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.36-768T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971310 | ||||||
| chr20:44971489
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.36-589G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971489 | ||||||
| chr20:44971538
|
G | T | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.36-540G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971538 | ||||||
| chr20:44971646
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.36-432C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971646 | ||||||
| chr20:44971665
|
C | CT | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0033others(13): Show | 16 | HG01361.hp2 HG02135.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-388dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971665 | |||||
| chr20:44971665
|
CT | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0174others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.36-388delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971665 | |||||
| chr20:44971665
|
CTT | C | 6 | a0002c0002t0003g0135a0002c0002t0003g0138a0002c0002t0003g0139others(3): Show | 6 | HG00099.hp2 HG01168.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-389_36-388delTT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971665 | |||||
| chr20:44971665
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0014 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.36-400_36-388delTT others(11): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 44971665 | |||||
| chr20:44971697
|
G | A | 2 | a0001c0001t0019g0177a0001c0001t0019g0178 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.36-381G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971697 | ||||||
| chr20:44971922
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.36-156C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971922 | ||||||
| chr20:44971992
|
A | G | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.36-86A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44971992 | ||||||
| chr20:44972032
|
C | G | 154 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.36-46C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44972032 | ||||||
| chr20:44972050
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.36-28T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44972050 | ||||||
| chr20:44972066
|
C | G | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.36-12C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 1/10 | chr20 | 44972066 | ||||||
| chr20:44972258
|
G | A | 1 | a0002c0002t0003g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116+100G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972258 | ||||||
| chr20:44972298
|
C | T | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+140C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972298 | ||||||
| chr20:44972415
|
C | A | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+257C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972415 | ||||||
| chr20:44972424
|
G | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.116+266G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972424 | ||||||
| chr20:44972505
|
A | G | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+347A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972505 | ||||||
| chr20:44972549
|
A | C | 1 | a0001c0001t0024g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.116+391A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972549 | ||||||
| chr20:44972639
|
T | C | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+481T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972639 | ||||||
| chr20:44972739
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0004g0005 | 2 | NA18950.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.116+581T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972739 | ||||||
| chr20:44972905
|
T | TA | 23 | a0001c0001t0011g0085a0002c0002t0003g0134a0002c0002t0003g0135others(20): Show | 23 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+762dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr20 | 44972905 | |||||
| chr20:44972933
|
T | G | 5 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(2): Show | 5 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+775T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972933 | ||||||
| chr20:44972972
|
C | T | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.116+814C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972972 | ||||||
| chr20:44972994
|
A | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.116+836A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44972994 | ||||||
| chr20:44973012
|
C | T | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.116+854C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973012 | ||||||
| chr20:44973083
|
G | A | 1 | a0001c0001t0004g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.116+925G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973083 | ||||||
| chr20:44973237
|
C | T | 1 | a0001c0001t0011g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.116+1079C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973237 | ||||||
| chr20:44973280
|
G | T | 184 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(181): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+1122G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973280 | ||||||
| chr20:44973390
|
C | T | 2 | a0002c0002t0003g0171a0002c0002t0003g0172 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.116+1232C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973390 | ||||||
| chr20:44973517
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.116+1359A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973517 | ||||||
| chr20:44973612
|
C | G | 1 | a0002c0002t0003g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.116+1454C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973612 | ||||||
| chr20:44973614
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0004g0323 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.116+1456C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973614 | ||||||
| chr20:44973837
|
A | G | 26 | a0001c0001t0002g0123a0001c0001t0006g0186a0001c0001t0006g0187others(23): Show | 26 | HG00621.hp1 HG02083.hp1 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.116+1679A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973837 | ||||||
| chr20:44973916
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116+1758A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44973916 | ||||||
| chr20:44974117
|
G | T | 1 | a0001c0001t0005g0072 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.116+1959G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974117 | ||||||
| chr20:44974186
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+2028A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974186 | ||||||
| chr20:44974245
|
T | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.116+2087T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974245 | ||||||
| chr20:44974313
|
C | T | 13 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(10): Show | 13 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.116+2155C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974313 | ||||||
| chr20:44974610
|
A | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0028others(7): Show | 10 | HG00597.hp2 HG06807.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+2452A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974610 | ||||||
| chr20:44974632
|
G | A | 6 | a0001c0001t0005g0002a0001c0001t0005g0073a0001c0001t0005g0074others(3): Show | 6 | HG01358.hp2 HG02109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+2474G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974632 | ||||||
| chr20:44974665
|
T | C | 1 | a0002c0002t0003g0185 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.116+2507T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974665 | ||||||
| chr20:44974732
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.116+2574T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974732 | ||||||
| chr20:44974825
|
G | A | 1 | a0001c0001t0019g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.116+2667G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974825 | ||||||
| chr20:44974882
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.116+2724A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974882 | ||||||
| chr20:44974892
|
A | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.116+2734A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44974892 | ||||||
| chr20:44975057
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.116+2899G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975057 | ||||||
| chr20:44975215
|
T | C | 2 | a0001c0001t0019g0177a0001c0001t0019g0178 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.116+3057T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975215 | ||||||
| chr20:44975362
|
C | T | 185 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.117-3081C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975362 | ||||||
| chr20:44975446
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.117-2997G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975446 | ||||||
| chr20:44975609
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.117-2834T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975609 | ||||||
| chr20:44975634
|
G | A | 4 | a0001c0001t0009g0204a0001c0001t0009g0205a0001c0001t0009g0206others(1): Show | 4 | NA18973.hp2 NA18980.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-2809G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44975634 | ||||||
| chr20:44976157
|
A | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117-2286A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976157 | ||||||
| chr20:44976398
|
C | T | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117-2045C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976398 | ||||||
| chr20:44976399
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0026g0274 | 2 | HG00280.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.117-2044G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976399 | ||||||
| chr20:44976661
|
A | G | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117-1782A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976661 | ||||||
| chr20:44976710
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.117-1733A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976710 | ||||||
| chr20:44976769
|
G | A | 1 | a0001c0001t0024g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.117-1674G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976769 | ||||||
| chr20:44976780
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 38 | HG00099.hp1 HG00597.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.117-1663C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976780 | ||||||
| chr20:44976871
|
A | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117-1572A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976871 | ||||||
| chr20:44976891
|
A | G | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.117-1552A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976891 | ||||||
| chr20:44976967
|
C | T | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117-1476C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44976967 | ||||||
| chr20:44977096
|
G | A | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-1347G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977096 | ||||||
| chr20:44977210
|
A | T | 10 | a0001c0001t0005g0059a0001c0001t0005g0064a0001c0001t0005g0065others(7): Show | 10 | HG00741.hp1 HG01106.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-1233A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977210 | ||||||
| chr20:44977320
|
A | G | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.117-1123A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977320 | ||||||
| chr20:44977339
|
T | C | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.117-1104T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977339 | ||||||
| chr20:44977387
|
T | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.117-1056T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977387 | ||||||
| chr20:44977454
|
T | C | 1 | a0001c0001t0004g0313 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.117-989T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977454 | ||||||
| chr20:44977526
|
G | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.117-917G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977526 | ||||||
| chr20:44977624
|
G | A | 4 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082others(1): Show | 4 | HG01167.hp1 HG01243.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-819G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977624 | ||||||
| chr20:44977755
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.117-688G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44977755 | ||||||
| chr20:44978137
|
T | G | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-306T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44978137 | ||||||
| chr20:44978200
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0026g0274 | 2 | HG00280.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.117-243T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 2/10 | chr20 | 44978200 | ||||||
| chr20:44978648
|
G | A | 1 | a0001c0001t0038g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.245+77G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44978648 | ||||||
| chr20:44978773
|
G | T | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+202G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44978773 | ||||||
| chr20:44978830
|
G | A | 1 | a0001c0001t0012g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245+259G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44978830 | ||||||
| chr20:44979216
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+645C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979216 | ||||||
| chr20:44979262
|
G | A | 1 | a0001c0001t0044g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+691G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979262 | ||||||
| chr20:44979429
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.245+858A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979429 | ||||||
| chr20:44979487
|
G | C | 72 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(69): Show | 72 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.245+916G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979487 | ||||||
| chr20:44979501
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+930C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979501 | ||||||
| chr20:44979548
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245+977G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979548 | ||||||
| chr20:44979770
|
C | CT | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.245+1208dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 44979770 | |||||
| chr20:44979939
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.245+1368C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44979939 | ||||||
| chr20:44980072
|
G | A | 4 | a0001c0001t0014g0256a0001c0001t0014g0257a0001c0001t0014g0258others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+1501G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980072 | ||||||
| chr20:44980284
|
G | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.246-1545G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980284 | ||||||
| chr20:44980337
|
G | C | 159 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.246-1492G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980337 | ||||||
| chr20:44980344
|
T | C | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.246-1485T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980344 | ||||||
| chr20:44980404
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.246-1425A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980404 | ||||||
| chr20:44980575
|
A | G | 157 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.246-1254A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980575 | ||||||
| chr20:44980603
|
A | G | 1 | a0001c0001t0006g0189 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.246-1226A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980603 | ||||||
| chr20:44980688
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.246-1141C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980688 | ||||||
| chr20:44980729
|
C | T | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246-1100C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980729 | ||||||
| chr20:44980731
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.246-1098C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980731 | ||||||
| chr20:44980824
|
C | T | 66 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.246-1005C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980824 | ||||||
| chr20:44980910
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0004g0323 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.246-919C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980910 | ||||||
| chr20:44980915
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.246-914A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44980915 | ||||||
| chr20:44981209
|
C | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.246-620C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981209 | ||||||
| chr20:44981406
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.246-423C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981406 | ||||||
| chr20:44981444
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.246-385T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981444 | ||||||
| chr20:44981533
|
T | A | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.246-296T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981533 | ||||||
| chr20:44981771
|
T | C | 1 | a0001c0001t0005g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246-58T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981771 | ||||||
| chr20:44981779
|
G | A | 1 | a0002c0002t0007g0158 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.246-50G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981779 | ||||||
| chr20:44981817
|
C | T | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.246-12C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 3/10 | chr20 | 44981817 | ||||||
| chr20:44982095
|
C | T | 4 | a0001c0001t0005g0069a0001c0001t0005g0071a0001c0001t0005g0072others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+152C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982095 | ||||||
| chr20:44982109
|
C | CT | 7 | a0001c0001t0001g0026a0001c0001t0010g0252a0001c0001t0014g0256others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+185dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44982109 | |||||
| chr20:44982109
|
CT | C | 141 | a0001c0001t0001g0051a0001c0001t0001g0267a0001c0001t0002g0003others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.360+185delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44982109 | |||||
| chr20:44982109
|
CTT | C | 9 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0008g0211others(6): Show | 9 | HG01346.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+184_360+185del others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44982109 | |||||
| chr20:44982161
|
G | T | 72 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(69): Show | 72 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.360+218G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982161 | ||||||
| chr20:44982224
|
C | G | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+281C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982224 | ||||||
| chr20:44982303
|
A | AT | 44 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(41): Show | 44 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.360+372dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44982303 | |||||
| chr20:44982326
|
T | G | 158 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.360+383T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982326 | ||||||
| chr20:44982498
|
T | G | 3 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0056 | 3 | HG02717.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.360+555T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982498 | ||||||
| chr20:44982502
|
A | G | 5 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(2): Show | 5 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+559A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982502 | ||||||
| chr20:44982589
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.360+646G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982589 | ||||||
| chr20:44982699
|
T | C | 120 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+756T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982699 | ||||||
| chr20:44982737
|
G | A | 120 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+794G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982737 | ||||||
| chr20:44982864
|
T | A | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+921T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982864 | ||||||
| chr20:44982866
|
T | TAGTTACT others(1): Show |
4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+923_360+924ins others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982866 | ||||||
| chr20:44982868
|
A | T | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+925A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982868 | ||||||
| chr20:44982872
|
G | T | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+929G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982872 | ||||||
| chr20:44982874
|
A | ACTTAGTA others(12): Show |
4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+931_360+932ins others(19): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982874 | ||||||
| chr20:44982996
|
C | T | 3 | a0001c0001t0018g0049a0001c0001t0018g0050a0001c0001t0035g0045 | 3 | HG02886.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.360+1053C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44982996 | ||||||
| chr20:44983439
|
A | G | 48 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.360+1496A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44983439 | ||||||
| chr20:44983457
|
A | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.360+1514A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44983457 | ||||||
| chr20:44983474
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.360+1531G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44983474 | ||||||
| chr20:44983681
|
T | C | 153 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.360+1738T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44983681 | ||||||
| chr20:44984098
|
G | GT | 54 | a0001c0001t0001g0011a0001c0001t0001g0302a0001c0001t0004g0251others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.360+2164dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984098 | |||||
| chr20:44984186
|
G | GT | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 163 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.360+2266dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984186 | |||||
| chr20:44984186
|
G | GTT | 74 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.360+2265_360+2266d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984186 | |||||
| chr20:44984186
|
G | GTTT | 49 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(46): Show | 49 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.360+2264_360+2266d others(5): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984186 | |||||
| chr20:44984186
|
G | GTTTT | 15 | a0001c0001t0001g0275a0001c0001t0002g0091a0001c0001t0002g0093others(12): Show | 15 | HG02074.hp2 HG02135.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+2263_360+2266d others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984186 | |||||
| chr20:44984225
|
T | C | 158 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.360+2282T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984225 | ||||||
| chr20:44984247
|
T | C | 2 | a0002c0002t0003g0160a0002c0002t0007g0159 | 2 | HG00323.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.360+2304T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984247 | ||||||
| chr20:44984256
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.360+2313G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984256 | ||||||
| chr20:44984260
|
A | T | 124 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.360+2317A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984260 | ||||||
| chr20:44984262
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.360+2319T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984262 | ||||||
| chr20:44984263
|
C | T | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+2320C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984263 | ||||||
| chr20:44984264
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.360+2321G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984264 | ||||||
| chr20:44984392
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.360+2449C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984392 | ||||||
| chr20:44984454
|
G | A | 1 | a0002c0002t0003g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+2511G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984454 | ||||||
| chr20:44984497
|
C | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.360+2554C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984497 | ||||||
| chr20:44984577
|
T | A | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.361-2555T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984577 | ||||||
| chr20:44984786
|
C | CT | 41 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0088others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.361-2335dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44984786 | |||||
| chr20:44984872
|
G | A | 158 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.361-2260G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984872 | ||||||
| chr20:44984887
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.361-2245T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44984887 | ||||||
| chr20:44985184
|
T | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.361-1948T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44985184 | ||||||
| chr20:44985607
|
T | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.361-1525T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44985607 | ||||||
| chr20:44985625
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.361-1507G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44985625 | ||||||
| chr20:44985861
|
G | A | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-1271G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44985861 | ||||||
| chr20:44985918
|
T | C | 12 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(9): Show | 12 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1214T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44985918 | ||||||
| chr20:44986183
|
G | A | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.361-949G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44986183 | ||||||
| chr20:44986188
|
A | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-944A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44986188 | ||||||
| chr20:44986208
|
G | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0095 | 2 | NA19004.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.361-924G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44986208 | ||||||
| chr20:44986512
|
CTT | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-617_361-616del others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 44986512 | |||||
| chr20:44986767
|
G | A | 48 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.361-365G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 4/10 | chr20 | 44986767 | ||||||
| chr20:44987513
|
A | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.525+217A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44987513 | ||||||
| chr20:44987713
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.525+417A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44987713 | ||||||
| chr20:44987804
|
T | C | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.525+508T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44987804 | ||||||
| chr20:44987967
|
G | GT | 12 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+681dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44987967 | |||||
| chr20:44987984
|
T | A | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.525+688T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44987984 | ||||||
| chr20:44988152
|
T | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+856T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988152 | ||||||
| chr20:44988170
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.525+874C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988170 | ||||||
| chr20:44988199
|
C | T | 66 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.525+903C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988199 | ||||||
| chr20:44988215
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+919A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988215 | ||||||
| chr20:44988237
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.525+941G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988237 | ||||||
| chr20:44988384
|
G | A | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.525+1088G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988384 | ||||||
| chr20:44988387
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.525+1091C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988387 | ||||||
| chr20:44988435
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.525+1139A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988435 | ||||||
| chr20:44988523
|
A | ATG | 7 | a0001c0001t0044g0176a0002c0002t0003g0150a0002c0002t0003g0151others(4): Show | 7 | HG01168.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+1237_525+1238d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988523 | |||||
| chr20:44988523
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0008g0213a0001c0001t0008g0223a0001c0001t0008g0224others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1229_525+1238d others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988523 | |||||
| chr20:44988523
|
A | ATGTGTGT others(5): Show |
3 | a0001c0001t0008g0212a0001c0001t0008g0214a0001c0001t0008g0215 | 3 | HG02572.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988523 | |||||
| chr20:44988523
|
A | ATGTGTGT others(7): Show |
33 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088others(30): Show | 33 | HG00423.hp2 HG01074.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988523 | |||||
| chr20:44988523
|
A | ATGTGTGT others(9): Show |
10 | a0001c0001t0002g0003a0001c0001t0002g0094a0001c0001t0002g0096others(7): Show | 10 | HG00597.hp1 HG02129.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988523 | |||||
| chr20:44988533
|
G | GTA | 23 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0227others(20): Show | 24 | HG00438.hp1 HG01167.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.525+1271_525+1272d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATA | 32 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.525+1269_525+1272d others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATA | 29 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0022others(26): Show | 29 | HG00597.hp2 HG01952.hp2 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+1267_525+1272d others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(1): Show |
26 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0020others(23): Show | 26 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.525+1265_525+1272d others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(3): Show |
14 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0174others(11): Show | 14 | HG01070.hp1 HG02083.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+1263_525+1272d others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(5): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0004g0314others(4): Show | 7 | HG00438.hp2 HG02040.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+1261_525+1272d others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(7): Show |
7 | a0001c0001t0006g0186a0001c0001t0006g0189a0001c0001t0006g0193others(4): Show | 7 | NA18612.hp1 NA18943.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+1259_525+1272d others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0004g0313a0001c0001t0016g0192 | 2 | NA18978.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.525+1257_525+1272d others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0010g0238 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.525+1255_525+1272d others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0006g0199 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.525+1253_525+1272d others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0004g0325 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.525+1251_525+1272d others(24): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTA | 5 | a0002c0002t0003g0138a0002c0002t0003g0146a0002c0002t0003g0147others(2): Show | 5 | HG00280.hp1 HG00323.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(1): Show |
5 | a0001c0001t0005g0059a0001c0001t0005g0067a0001c0001t0005g0071others(2): Show | 5 | HG00735.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(3): Show |
7 | a0001c0001t0005g0058a0001c0001t0005g0066a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(5): Show |
8 | a0001c0001t0005g0002a0001c0001t0005g0057a0001c0001t0005g0061others(5): Show | 8 | HG01358.hp2 HG02451.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+1238_525+1239i others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(7): Show |
3 | a0001c0001t0005g0074a0001c0001t0005g0080a0001c0001t0046g0079 | 3 | HG01167.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0005g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(11): Show |
2 | a0001c0001t0005g0055a0001c0001t0005g0073 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(13): Show |
1 | a0001c0001t0005g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(15): Show |
1 | a0001c0001t0005g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(24): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTATAT others(21): Show |
1 | a0001c0001t0005g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.525+1238_525+1239i others(30): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTAT others(3): Show |
1 | a0001c0001t0005g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(9): Show |
2 | a0001c0001t0012g0047a0001c0001t0012g0048 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0035g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(13): Show |
3 | a0001c0001t0012g0046a0001c0001t0012g0053a0001c0001t0034g0052 | 3 | HG02027.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(15): Show |
2 | a0001c0001t0018g0049a0001c0001t0018g0050 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(24): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(7): Show |
2 | a0001c0001t0008g0221a0001c0001t0037g0222 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.525+1238_525+1239i others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0038g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.525+1238_525+1239i others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.525+1238_525+1239i others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
GTA | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0233others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+1271_525+1272d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
GTATATA | G | 5 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0007g0168others(2): Show | 5 | HG01361.hp1 HG01517.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1267_525+1272d others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
GTATATAT others(3): Show |
G | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1263_525+1272d others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988533
|
GTATATAT others(7): Show |
G | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.525+1259_525+1272d others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988533 | |||||
| chr20:44988535
|
A | G | 73 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(70): Show | 73 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.525+1239A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988535 | ||||||
| chr20:44988537
|
A | G | 55 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.525+1241A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988537 | ||||||
| chr20:44988539
|
A | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(42): Show | 45 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.525+1243A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988539 | ||||||
| chr20:44988541
|
A | ATGTGTG | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1246_525+1247i others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44988541 | |||||
| chr20:44988541
|
A | G | 49 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(46): Show | 49 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.525+1245A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988541 | ||||||
| chr20:44988543
|
A | G | 50 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(47): Show | 50 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.525+1247A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988543 | ||||||
| chr20:44988545
|
A | G | 42 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088others(39): Show | 42 | HG00423.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.525+1249A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988545 | ||||||
| chr20:44988547
|
A | G | 5 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088others(2): Show | 5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+1251A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988547 | ||||||
| chr20:44988549
|
A | G | 2 | a0001c0001t0042g0128a0002c0002t0043g0084 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.525+1253A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988549 | ||||||
| chr20:44988551
|
A | G | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.525+1255A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988551 | ||||||
| chr20:44988585
|
C | G | 115 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.525+1289C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988585 | ||||||
| chr20:44988865
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.525+1569C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44988865 | ||||||
| chr20:44989137
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.525+1841G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989137 | ||||||
| chr20:44989152
|
A | T | 1 | a0001c0001t0015g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.525+1856A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989152 | ||||||
| chr20:44989263
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.525+1967G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989263 | ||||||
| chr20:44989367
|
C | T | 18 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(15): Show | 18 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.525+2071C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989367 | ||||||
| chr20:44989489
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.525+2193A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989489 | ||||||
| chr20:44989533
|
TTC | T | 47 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.525+2242_525+2243d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44989533 | |||||
| chr20:44989881
|
A | G | 31 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(28): Show | 31 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.525+2585A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989881 | ||||||
| chr20:44989916
|
C | T | 2 | a0002c0002t0003g0160a0002c0002t0007g0159 | 2 | HG00323.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.525+2620C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989916 | ||||||
| chr20:44989998
|
C | T | 2 | a0001c0001t0017g0031a0001c0001t0017g0032 | 2 | HG00597.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.525+2702C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44989998 | ||||||
| chr20:44990017
|
G | C | 1 | a0002c0002t0007g0162 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.525+2721G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44990017 | ||||||
| chr20:44990175
|
A | C | 1 | a0001c0001t0044g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.525+2879A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44990175 | ||||||
| chr20:44990334
|
C | A | 4 | a0001c0001t0002g0090a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+3038C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44990334 | ||||||
| chr20:44990397
|
C | CT | 44 | a0001c0001t0001g0234a0001c0001t0002g0003a0001c0001t0002g0043others(41): Show | 44 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.525+3113dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44990397 | |||||
| chr20:44990554
|
T | TCTCCGGT others(523): Show |
1 | a0001c0001t0001g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+3270_525+3271i others(532): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44990554 | |||||
| chr20:44990577
|
T | C | 1 | a0001c0001t0005g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.525+3281T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44990577 | ||||||
| chr20:44991116
|
G | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.525+3820G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991116 | ||||||
| chr20:44991239
|
T | A | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3851T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991239 | ||||||
| chr20:44991360
|
C | T | 2 | a0001c0001t0008g0221a0001c0001t0037g0222 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526-3730C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991360 | ||||||
| chr20:44991399
|
A | G | 1 | a0002c0002t0007g0156 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.526-3691A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991399 | ||||||
| chr20:44991407
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-3683A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991407 | ||||||
| chr20:44991479
|
C | A | 1 | a0001c0001t0044g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.526-3611C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991479 | ||||||
| chr20:44991626
|
C | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-3464C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991626 | ||||||
| chr20:44991657
|
T | C | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3433T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991657 | ||||||
| chr20:44991681
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526-3409G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991681 | ||||||
| chr20:44991731
|
C | A | 1 | a0001c0001t0006g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.526-3359C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991731 | ||||||
| chr20:44991778
|
T | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.526-3312T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991778 | ||||||
| chr20:44991814
|
C | T | 4 | a0002c0002t0003g0139a0002c0002t0003g0143a0002c0002t0003g0145others(1): Show | 4 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-3276C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991814 | ||||||
| chr20:44991864
|
A | G | 4 | a0003c0003t0001g0279a0003c0003t0001g0298a0003c0003t0001g0307others(1): Show | 4 | HG02040.hp2 HG02155.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-3226A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991864 | ||||||
| chr20:44991912
|
C | G | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.526-3178C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991912 | ||||||
| chr20:44991940
|
A | G | 47 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.526-3150A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44991940 | ||||||
| chr20:44992058
|
T | G | 1 | a0001c0001t0003g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526-3032T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44992058 | ||||||
| chr20:44992215
|
A | G | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.526-2875A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44992215 | ||||||
| chr20:44992267
|
A | AT | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.526-2814dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44992267 | |||||
| chr20:44992310
|
G | A | 1 | a0001c0001t0015g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.526-2780G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44992310 | ||||||
| chr20:44992469
|
C | T | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.526-2621C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44992469 | ||||||
| chr20:44993013
|
A | G | 1 | a0002c0002t0003g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.526-2077A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993013 | ||||||
| chr20:44993050
|
T | A | 14 | a0001c0001t0005g0059a0001c0001t0005g0064a0001c0001t0005g0065others(11): Show | 14 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.526-2040T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993050 | ||||||
| chr20:44993198
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-1892T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993198 | ||||||
| chr20:44993253
|
T | TAC | 110 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.526-1827_526-1826d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44993253 | |||||
| chr20:44993253
|
T | TACAC | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-1829_526-1826d others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44993253 | |||||
| chr20:44993386
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526-1704T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993386 | ||||||
| chr20:44993423
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.526-1667T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993423 | ||||||
| chr20:44993462
|
T | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.526-1628T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993462 | ||||||
| chr20:44993574
|
T | C | 1 | a0002c0002t0007g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.526-1516T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993574 | ||||||
| chr20:44993665
|
T | C | 6 | a0001c0001t0005g0002a0001c0001t0005g0073a0001c0001t0005g0074others(3): Show | 6 | HG01358.hp2 HG02109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-1425T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993665 | ||||||
| chr20:44993798
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.526-1292G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993798 | ||||||
| chr20:44993911
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.526-1179G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44993911 | ||||||
| chr20:44994253
|
A | ATT | 26 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0004g0005others(23): Show | 26 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.526-836_526-835dup others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44994253 | |||||
| chr20:44994284
|
G | C | 1 | a0005c0006t0013g0216 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.526-806G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44994284 | ||||||
| chr20:44994594
|
T | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-496T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44994594 | ||||||
| chr20:44994617
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.526-473A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44994617 | ||||||
| chr20:44994990
|
T | C | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.526-100T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44994990 | ||||||
| chr20:44994992
|
GT | G | 12 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(9): Show | 12 | HG00735.hp1 HG01081.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-85delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 44994992 | |||||
| chr20:44995017
|
C | T | 115 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.526-73C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 5/10 | chr20 | 44995017 | ||||||
| chr20:44995604
|
T | TG | 9 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(6): Show | 9 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+347_693+348ins others(1): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995604 | ||||||
| chr20:44995605
|
C | A | 10 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(7): Show | 10 | HG01261.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+348C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995605 | ||||||
| chr20:44995605
|
C | CA | 136 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0039others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.693+372dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr20 | 44995605 | |||||
| chr20:44995605
|
C | CAA | 34 | a0001c0001t0002g0124a0001c0001t0005g0041a0001c0001t0005g0042others(31): Show | 34 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.693+371_693+372dup others(2): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr20 | 44995605 | |||||
| chr20:44995605
|
C | G | 1 | a0001c0001t0037g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.693+348C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995605 | ||||||
| chr20:44995605
|
CA | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0247others(5): Show | 8 | HG01070.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+372delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr20 | 44995605 | |||||
| chr20:44995635
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 46 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.693+378A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995635 | ||||||
| chr20:44995694
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.693+437G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995694 | ||||||
| chr20:44995952
|
A | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.693+695A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44995952 | ||||||
| chr20:44996141
|
G | C | 1 | a0001c0001t0012g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.693+884G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996141 | ||||||
| chr20:44996275
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.694-894A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996275 | ||||||
| chr20:44996336
|
C | G | 18 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(15): Show | 18 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-833C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996336 | ||||||
| chr20:44996359
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.694-810G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996359 | ||||||
| chr20:44996412
|
C | T | 174 | a0001c0001t0001g0051a0001c0001t0001g0236a0001c0001t0001g0237others(171): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.694-757C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996412 | ||||||
| chr20:44996450
|
T | G | 1 | a0001c0001t0004g0312 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.694-719T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | chr20 | 44996450 | ||||||
| chr20:44996924
|
CTTGA | C | 66 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.694-239_694-236del others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr20 | 44996924 | |||||
| chr20:44997389
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.831+83A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997389 | ||||||
| chr20:44997429
|
C | T | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.831+123C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997429 | ||||||
| chr20:44997515
|
T | C | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.831+209T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997515 | ||||||
| chr20:44997544
|
G | A | 4 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+238G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997544 | ||||||
| chr20:44997596
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.831+290G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997596 | ||||||
| chr20:44997622
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.831+316A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997622 | ||||||
| chr20:44997652
|
G | A | 8 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0193others(5): Show | 8 | NA18612.hp1 NA18966.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+346G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997652 | ||||||
| chr20:44997696
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.831+390C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997696 | ||||||
| chr20:44997973
|
T | A | 1 | a0001c0001t0004g0310 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.831+667T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44997973 | ||||||
| chr20:44998055
|
T | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.831+749T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998055 | ||||||
| chr20:44998363
|
C | T | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.831+1057C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998363 | ||||||
| chr20:44998401
|
T | C | 1 | a0001c0001t0014g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+1095T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998401 | ||||||
| chr20:44998446
|
C | T | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+1140C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998446 | ||||||
| chr20:44998486
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.831+1180G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998486 | ||||||
| chr20:44998516
|
T | C | 3 | a0001c0001t0014g0256a0001c0001t0014g0257a0001c0001t0014g0258 | 3 | HG02647.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.831+1210T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998516 | ||||||
| chr20:44998542
|
A | G | 72 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(69): Show | 72 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.831+1236A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998542 | ||||||
| chr20:44998599
|
A | G | 2 | a0002c0002t0003g0134a0002c0002t0003g0155 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.831+1293A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998599 | ||||||
| chr20:44998672
|
G | T | 25 | a0001c0001t0001g0267a0001c0001t0001g0269a0001c0001t0001g0271others(22): Show | 25 | HG00438.hp1 HG01496.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.831+1366G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998672 | ||||||
| chr20:44998710
|
G | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.831+1404G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998710 | ||||||
| chr20:44998934
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.832-1458G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998934 | ||||||
| chr20:44998950
|
G | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.832-1442G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44998950 | ||||||
| chr20:44999067
|
C | CA | 32 | a0001c0001t0001g0051a0001c0001t0001g0271a0001c0001t0001g0281others(29): Show | 32 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.832-1313dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr20 | 44999067 | |||||
| chr20:44999067
|
C | CAA | 17 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(14): Show | 17 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-1314_832-1313d others(4): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr20 | 44999067 | |||||
| chr20:44999067
|
C | CAAA | 42 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(39): Show | 42 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.832-1315_832-1313d others(5): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr20 | 44999067 | |||||
| chr20:44999110
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-1282C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999110 | ||||||
| chr20:44999135
|
G | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.832-1257G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999135 | ||||||
| chr20:44999177
|
AG | A | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.832-1213delG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr20 | 44999177 | |||||
| chr20:44999312
|
T | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-1080T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999312 | ||||||
| chr20:44999405
|
A | T | 2 | a0001c0001t0012g0047a0001c0001t0012g0048 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.832-987A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999405 | ||||||
| chr20:44999512
|
A | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.832-880A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999512 | ||||||
| chr20:44999546
|
C | A | 1 | a0001c0001t0038g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832-846C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999546 | ||||||
| chr20:44999826
|
T | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832-566T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 44999826 | ||||||
| chr20:45000006
|
G | A | 1 | a0002c0002t0003g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.832-386G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 45000006 | ||||||
| chr20:45000030
|
A | C | 4 | a0001c0001t0005g0060a0001c0001t0005g0061a0001c0001t0005g0062others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-362A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 45000030 | ||||||
| chr20:45000036
|
G | A | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.832-356G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 45000036 | ||||||
| chr20:45000343
|
A | C | 1 | a0002c0002t0003g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.832-49A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 7/10 | chr20 | 45000343 | ||||||
| chr20:45000552
|
C | T | 26 | a0001c0001t0001g0266a0001c0001t0006g0186a0001c0001t0006g0187others(23): Show | 26 | HG00621.hp1 HG02027.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.960+32C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000552 | ||||||
| chr20:45000744
|
C | A | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+224C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000744 | ||||||
| chr20:45000746
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.960+226T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000746 | ||||||
| chr20:45000791
|
G | A | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.960+271G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000791 | ||||||
| chr20:45000871
|
T | C | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.961-296T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000871 | ||||||
| chr20:45000888
|
C | G | 1 | a0001c0001t0002g0095 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.961-279C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000888 | ||||||
| chr20:45000888
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.961-279C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000888 | ||||||
| chr20:45000906
|
G | T | 1 | a0001c0001t0017g0032 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.961-261G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000906 | ||||||
| chr20:45000946
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-221A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45000946 | ||||||
| chr20:45001074
|
C | T | 1 | a0001c0001t0026g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.961-93C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45001074 | ||||||
| chr20:45001123
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-44C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 8/10 | chr20 | 45001123 | ||||||
| chr20:45001551
|
A | G | 8 | a0001c0001t0001g0267a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | NA18941.hp1 NA18941.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147+198A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45001551 | ||||||
| chr20:45001858
|
C | G | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1147+505C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45001858 | ||||||
| chr20:45001858
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1147+505C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45001858 | ||||||
| chr20:45001974
|
C | T | 47 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1147+621C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45001974 | ||||||
| chr20:45002576
|
A | G | 1 | a0001c0001t0013g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1147+1223A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45002576 | ||||||
| chr20:45002586
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1147+1233A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45002586 | ||||||
| chr20:45002654
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1147+1301C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45002654 | ||||||
| chr20:45002795
|
G | A | 185 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1147+1442G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45002795 | ||||||
| chr20:45003028
|
A | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1147+1675A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003028 | ||||||
| chr20:45003060
|
G | T | 1 | a0002c0002t0003g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1147+1707G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003060 | ||||||
| chr20:45003202
|
A | G | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1147+1849A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003202 | ||||||
| chr20:45003368
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1147+2015G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003368 | ||||||
| chr20:45003712
|
A | AT | 26 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0051others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1147+2379dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45003712 | |||||
| chr20:45003742
|
G | A | 2 | a0002c0002t0007g0158a0002c0002t0007g0163 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1147+2389G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003742 | ||||||
| chr20:45003791
|
A | G | 2 | a0002c0002t0003g0160a0002c0002t0007g0159 | 2 | HG00323.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1147+2438A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003791 | ||||||
| chr20:45003810
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147+2457G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003810 | ||||||
| chr20:45003895
|
T | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1147+2542T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45003895 | ||||||
| chr20:45003986
|
T | TGGAATTA others(48): Show |
1 | a0001c0001t0001g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1147+2634_1147+268 others(59): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45003986 | |||||
| chr20:45004013
|
C | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147+2660C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004013 | ||||||
| chr20:45004118
|
C | T | 1 | a0001c0001t0005g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1147+2765C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004118 | ||||||
| chr20:45004135
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0025 | 2 | HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1147+2782G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004135 | ||||||
| chr20:45004298
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1147+2945G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004298 | ||||||
| chr20:45004317
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1147+2964A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004317 | ||||||
| chr20:45004470
|
A | T | 1 | a0001c0001t0004g0311 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1147+3117A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004470 | ||||||
| chr20:45004523
|
G | GT | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1147+3180dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45004523 | |||||
| chr20:45004767
|
CTTTTTTC others(12): Show |
C | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1147+3415_1147+343 others(23): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004767 | ||||||
| chr20:45004777
|
T | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1147+3424T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004777 | ||||||
| chr20:45004854
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1147+3501C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004854 | ||||||
| chr20:45004855
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1147+3502G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004855 | ||||||
| chr20:45004962
|
A | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1147+3609A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45004962 | ||||||
| chr20:45005013
|
C | T | 1 | a0001c0001t0004g0297 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1147+3660C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005013 | ||||||
| chr20:45005018
|
G | T | 4 | a0001c0001t0002g0090a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+3665G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005018 | ||||||
| chr20:45005048
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1147+3695G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005048 | ||||||
| chr20:45005109
|
C | T | 2 | a0001c0001t0018g0049a0001c0001t0018g0050 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1147+3756C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005109 | ||||||
| chr20:45005470
|
C | A | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1147+4117C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005470 | ||||||
| chr20:45005505
|
G | C | 1 | a0002c0002t0007g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1147+4152G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005505 | ||||||
| chr20:45005642
|
T | C | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1147+4289T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005642 | ||||||
| chr20:45005647
|
C | CA | 53 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0033others(50): Show | 53 | HG00438.hp1 HG00741.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1147+4314dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45005647 | |||||
| chr20:45005647
|
C | CAA | 10 | a0001c0001t0004g0314a0001c0001t0005g0002a0001c0001t0005g0057others(7): Show | 10 | HG00438.hp2 HG01358.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1147+4313_1147+431 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45005647 | |||||
| chr20:45005647
|
CA | C | 41 | a0001c0001t0001g0247a0001c0001t0002g0003a0001c0001t0002g0043others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.1147+4314delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45005647 | |||||
| chr20:45005657
|
A | C | 1 | a0001c0001t0001g0287 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1147+4304A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005657 | ||||||
| chr20:45005661
|
A | C | 2 | a0001c0001t0006g0193a0001c0001t0022g0190 | 2 | NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1147+4308A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005661 | ||||||
| chr20:45005662
|
A | C | 1 | a0001c0001t0026g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1147+4309A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005662 | ||||||
| chr20:45005668
|
C | A | 3 | a0001c0001t0004g0261a0001c0001t0010g0242a0001c0001t0010g0254 | 3 | HG02735.hp2 NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1147+4315C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005668 | ||||||
| chr20:45005698
|
G | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1147+4345G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005698 | ||||||
| chr20:45005699
|
A | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1147+4346A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005699 | ||||||
| chr20:45005722
|
G | A | 34 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(31): Show | 34 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1147+4369G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005722 | ||||||
| chr20:45005861
|
TTTTTCTC others(48): Show |
T | 1 | a0001c0001t0001g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1147+4519_1147+457 others(59): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45005861 | |||||
| chr20:45005892
|
G | T | 1 | a0001c0001t0024g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1147+4539G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45005892 | ||||||
| chr20:45006021
|
T | C | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1147+4668T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006021 | ||||||
| chr20:45006191
|
A | T | 1 | a0001c0001t0006g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1147+4838A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006191 | ||||||
| chr20:45006253
|
G | GTATT | 47 | a0001c0001t0001g0035a0001c0001t0011g0132a0002c0002t0003g0134others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1147+4925_1147+492 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45006253 | |||||
| chr20:45006253
|
G | GTATTTAT others(5): Show |
1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1147+4917_1147+492 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45006253 | |||||
| chr20:45006253
|
G | GTATTTAT others(9): Show |
1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1147+4913_1147+492 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45006253 | |||||
| chr20:45006253
|
GTATT | G | 3 | a0001c0001t0001g0290a0001c0001t0009g0209a0001c0001t0046g0079 | 3 | HG00621.hp1 HG01167.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1147+4925_1147+492 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45006253 | |||||
| chr20:45006257
|
T | G | 1 | a0001c0001t0027g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1147+4904T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006257 | ||||||
| chr20:45006325
|
C | T | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1147+4972C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006325 | ||||||
| chr20:45006332
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0027g0038 | 2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1147+4979G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006332 | ||||||
| chr20:45006569
|
T | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1147+5216T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006569 | ||||||
| chr20:45006691
|
C | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1147+5338C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45006691 | ||||||
| chr20:45007013
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0001g0291a0001c0001t0001g0303 | 3 | HG02129.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1147+5660G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007013 | ||||||
| chr20:45007030
|
G | A | 1 | a0002c0005t0003g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1147+5677G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007030 | ||||||
| chr20:45007033
|
A | G | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+5680A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007033 | ||||||
| chr20:45007043
|
T | TTTTG | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147+5710_1147+571 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45007043 | |||||
| chr20:45007138
|
T | C | 1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1147+5785T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007138 | ||||||
| chr20:45007151
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1147+5798A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007151 | ||||||
| chr20:45007175
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1147+5822A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007175 | ||||||
| chr20:45007420
|
G | A | 6 | a0001c0001t0004g0251a0001c0001t0004g0259a0001c0001t0004g0261others(3): Show | 6 | HG01109.hp2 HG01123.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+6067G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007420 | ||||||
| chr20:45007521
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6168C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007521 | ||||||
| chr20:45007525
|
T | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6172T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007525 | ||||||
| chr20:45007533
|
C | T | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1147+6180C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007533 | ||||||
| chr20:45007542
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6189A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007542 | ||||||
| chr20:45007546
|
C | CAAAA | 7 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0047others(4): Show | 7 | HG01081.hp1 HG02698.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1147+6196_1147+619 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45007546 | |||||
| chr20:45007553
|
C | A | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6200C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007553 | ||||||
| chr20:45007557
|
C | A | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6204C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007557 | ||||||
| chr20:45007561
|
C | A | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+6208C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007561 | ||||||
| chr20:45007609
|
G | A | 8 | a0001c0001t0001g0267a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | NA18941.hp1 NA18941.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147+6256G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007609 | ||||||
| chr20:45007671
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1147+6318A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007671 | ||||||
| chr20:45007770
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1147+6417A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007770 | ||||||
| chr20:45007890
|
C | T | 1 | a0002c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1147+6537C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45007890 | ||||||
| chr20:45008055
|
G | A | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+6702G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008055 | ||||||
| chr20:45008110
|
G | A | 4 | a0001c0001t0002g0090a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+6757G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008110 | ||||||
| chr20:45008130
|
C | G | 6 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(3): Show | 6 | HG01891.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+6777C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008130 | ||||||
| chr20:45008189
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1147+6836G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008189 | ||||||
| chr20:45008274
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1147+6921C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008274 | ||||||
| chr20:45008320
|
G | A | 18 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(15): Show | 18 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1147+6967G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008320 | ||||||
| chr20:45008333
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1147+6980G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008333 | ||||||
| chr20:45008462
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1147+7109G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008462 | ||||||
| chr20:45008478
|
C | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147+7125C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008478 | ||||||
| chr20:45008593
|
C | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1147+7240C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008593 | ||||||
| chr20:45008858
|
C | T | 1 | a0003c0003t0045g0305 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1147+7505C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45008858 | ||||||
| chr20:45009328
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1147+7975C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009328 | ||||||
| chr20:45009338
|
C | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1147+7985C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009338 | ||||||
| chr20:45009563
|
C | G | 1 | a0001c0001t0006g0197 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1147+8210C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009563 | ||||||
| chr20:45009576
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1147+8223A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009576 | ||||||
| chr20:45009620
|
G | A | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147+8267G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009620 | ||||||
| chr20:45009691
|
T | C | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1147+8338T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009691 | ||||||
| chr20:45009811
|
T | G | 5 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(2): Show | 5 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1147+8458T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009811 | ||||||
| chr20:45009871
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1147+8518C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45009871 | ||||||
| chr20:45010017
|
ATTTC | A | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1147+8672_1147+867 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45010017 | |||||
| chr20:45010091
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1147+8738C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010091 | ||||||
| chr20:45010138
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1147+8785G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010138 | ||||||
| chr20:45010190
|
T | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+8837T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010190 | ||||||
| chr20:45010392
|
T | C | 1 | a0001c0001t0008g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1147+9039T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010392 | ||||||
| chr20:45010645
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1147+9292T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010645 | ||||||
| chr20:45010865
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1147+9512G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45010865 | ||||||
| chr20:45011220
|
A | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147+9867A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011220 | ||||||
| chr20:45011283
|
G | A | 3 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0319 | 3 | NA18947.hp2 NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1147+9930G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011283 | ||||||
| chr20:45011350
|
C | G | 115 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1147+9997C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011350 | ||||||
| chr20:45011675
|
A | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147+10322A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011675 | ||||||
| chr20:45011704
|
C | CATATATA others(3): Show |
1 | a0001c0001t0019g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1147+10354_1147+10 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011704 | |||||
| chr20:45011708
|
C | CAT | 21 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0236others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1147+10376_1147+10 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATAT | 28 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0179others(25): Show | 28 | HG00423.hp2 HG00597.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1147+10374_1147+10 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATAT | 8 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0095others(5): Show | 8 | HG02135.hp2 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147+10372_1147+10 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(1): Show |
16 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088others(13): Show | 16 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1147+10370_1147+10 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(3): Show |
4 | a0001c0001t0004g0310a0001c0001t0008g0213a0001c0001t0008g0214others(1): Show | 4 | HG02622.hp2 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147+10368_1147+10 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(5): Show |
8 | a0001c0001t0004g0313a0001c0001t0004g0324a0001c0001t0004g0325others(5): Show | 8 | HG01261.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1147+10366_1147+10 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(7): Show |
3 | a0001c0001t0005g0061a0001c0001t0005g0062a0001c0001t0008g0211 | 3 | HG02717.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1147+10364_1147+10 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(9): Show |
1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+10362_1147+10 others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(11): Show |
9 | a0001c0001t0005g0042a0001c0001t0005g0064a0001c0001t0005g0068others(6): Show | 9 | HG00741.hp1 HG01106.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1147+10360_1147+10 others(24): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(13): Show |
4 | a0001c0001t0005g0071a0001c0001t0021g0070a0001c0001t0044g0176others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+10358_1147+10 others(26): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(15): Show |
1 | a0001c0001t0005g0066 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1147+10356_1147+10 others(28): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(17): Show |
2 | a0001c0001t0005g0056a0002c0002t0003g0145 | 2 | HG03540.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(30): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(21): Show |
2 | a0002c0002t0003g0143a0002c0002t0007g0163 | 2 | HG01123.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(34): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(23): Show |
1 | a0002c0002t0003g0139 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(36): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | CATATATA others(27): Show |
1 | a0002c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(40): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011708 | |||||
| chr20:45011708
|
C | T | 1 | a0001c0001t0019g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1147+10355C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011708 | ||||||
| chr20:45011723
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1147+10372_1147+10 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011723 | |||||
| chr20:45011726
|
TA | T | 3 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0133 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1147+10374delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011726 | ||||||
| chr20:45011727
|
A | T | 1 | a0001c0001t0011g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1147+10374A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011727 | ||||||
| chr20:45011727
|
ATATTTTT others(4): Show |
A | 1 | a0002c0002t0003g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1147+10376_1147+10 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011727 | |||||
| chr20:45011729
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0005g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(26): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0005g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(28): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0005g0058a0001c0001t0005g0065 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(25): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0005g0055a0001c0001t0005g0059 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(26): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0005g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0005g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
A | T | 4 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147+10376A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011729 | ||||||
| chr20:45011729
|
AT | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0249a0001c0001t0001g0304others(3): Show | 6 | HG00438.hp1 HG01081.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+10393delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011729
|
ATTTT | A | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 HG06807.hp1 others(22): Show |
intron_variant | MODIFIER | c.1147+10390_1147+10 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45011729 | |||||
| chr20:45011730
|
T | TA | 8 | a0001c0001t0001g0029a0001c0001t0001g0227a0001c0001t0001g0275others(5): Show | 8 | HG00280.hp2 HG02055.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(7): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(4): Show |
1 | a0002c0002t0007g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(6): Show |
2 | a0002c0002t0003g0171a0002c0002t0007g0156 | 2 | HG02486.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(19): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(8): Show |
3 | a0001c0001t0004g0314a0001c0001t0005g0060a0002c0002t0003g0172 | 3 | HG00438.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(21): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(10): Show |
5 | a0001c0001t0005g0002a0001c0001t0005g0075a0002c0002t0003g0151others(2): Show | 5 | HG01358.hp2 HG03017.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(23): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(12): Show |
10 | a0002c0002t0003g0144a0002c0002t0003g0152a0002c0002t0003g0153others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(25): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(14): Show |
2 | a0002c0002t0003g0147a0002c0002t0003g0183 | 2 | HG00280.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(27): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(16): Show |
7 | a0001c0001t0005g0069a0002c0002t0003g0138a0002c0002t0003g0146others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(29): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(18): Show |
4 | a0001c0001t0005g0041a0002c0002t0003g0182a0002c0002t0007g0136others(1): Show | 4 | HG02717.hp1 HG03239.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(31): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(20): Show |
1 | a0002c0002t0007g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(33): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(22): Show |
3 | a0002c0002t0003g0166a0002c0002t0007g0164a0002c0002t0036g0167 | 3 | HG00639.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1147+10377_1147+10 others(35): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011730
|
T | TATATATA others(30): Show |
1 | a0002c0002t0007g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1147+10377_1147+10 others(43): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011730 | ||||||
| chr20:45011731
|
T | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(190): Show | 194 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1147+10378T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011731 | ||||||
| chr20:45011732
|
T | A | 45 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0227others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1147+10379T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011732 | ||||||
| chr20:45011733
|
T | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1147+10380T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011733 | ||||||
| chr20:45011734
|
T | A | 28 | a0001c0001t0001g0029a0001c0001t0004g0297a0001c0001t0004g0312others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1147+10381T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011734 | ||||||
| chr20:45011735
|
T | A | 76 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0022others(73): Show | 76 | HG00423.hp2 HG01074.hp2 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.1147+10382T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011735 | ||||||
| chr20:45011735
|
T | TATATATA others(32): Show |
1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1147+10382_1147+10 others(45): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011735 | ||||||
| chr20:45011736
|
T | A | 21 | a0001c0001t0006g0201a0001c0001t0033g0083a0002c0002t0003g0160others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1147+10383T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011736 | ||||||
| chr20:45011737
|
T | A | 26 | a0001c0001t0002g0003a0001c0001t0002g0089a0001c0001t0002g0090others(23): Show | 26 | HG01123.hp1 HG01515.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1147+10384T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011737 | ||||||
| chr20:45011738
|
T | A | 11 | a0002c0002t0003g0180a0002c0002t0003g0181a0002c0002t0003g0182others(8): Show | 11 | HG00099.hp2 HG00639.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1147+10385T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011738 | ||||||
| chr20:45011740
|
T | A | 6 | a0002c0002t0003g0180a0002c0002t0003g0181a0002c0002t0003g0182others(3): Show | 6 | HG01243.hp2 HG01517.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+10387T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45011740 | ||||||
| chr20:45012097
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1147+10744G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012097 | ||||||
| chr20:45012195
|
C | T | 5 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147+10842C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012195 | ||||||
| chr20:45012255
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1147+10902C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012255 | ||||||
| chr20:45012314
|
G | T | 1 | a0005c0006t0013g0216 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1147+10961G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012314 | ||||||
| chr20:45012652
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1147+11299G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012652 | ||||||
| chr20:45012723
|
C | G | 1 | a0001c0001t0001g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1147+11370C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012723 | ||||||
| chr20:45012764
|
T | C | 1 | a0002c0002t0007g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1147+11411T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012764 | ||||||
| chr20:45012770
|
TTATA | T | 4 | a0002c0002t0003g0180a0002c0002t0003g0181a0002c0002t0003g0182others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+11422_1147+11 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012770 | |||||
| chr20:45012782
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1147+11429T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012782 | ||||||
| chr20:45012794
|
TTC | T | 42 | a0001c0001t0011g0132a0002c0002t0003g0134a0002c0002t0003g0135others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1147+11443_1147+11 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012794 | |||||
| chr20:45012795
|
TC | T | 4 | a0002c0002t0003g0180a0002c0002t0003g0181a0002c0002t0003g0182others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147+11443delC | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012795 | ||||||
| chr20:45012796
|
C | CT | 84 | a0001c0001t0001g0051a0001c0001t0002g0111a0001c0001t0005g0002others(81): Show | 84 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.1147+11445dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012796 | |||||
| chr20:45012796
|
C | CTT | 12 | a0001c0001t0005g0064a0001c0001t0008g0211a0001c0001t0008g0212others(9): Show | 12 | HG01106.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1147+11444_1147+11 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012796 | |||||
| chr20:45012798
|
TC | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0002g0092others(2): Show | 5 | HG01099.hp2 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147+11446delC | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012798 | ||||||
| chr20:45012799
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1147+11446C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012799 | ||||||
| chr20:45012846
|
C | T | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1147+11493C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45012846 | ||||||
| chr20:45012948
|
AT | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0239a0001c0001t0001g0245others(3): Show | 6 | HG00738.hp1 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+11626delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATT | A | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1147+11625_1147+11 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATTT | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 111 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1147+11624_1147+11 others(9): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATTTT | A | 37 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0271others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1147+11623_1147+11 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATTTTT | A | 84 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(81): Show | 84 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1147+11622_1147+11 others(11): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATTTTTT | A | 53 | a0001c0001t0002g0099a0001c0001t0002g0123a0001c0001t0005g0067others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1147+11621_1147+11 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45012948
|
ATTTTTTT others(5): Show |
A | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+11615_1147+11 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45012948 | |||||
| chr20:45013007
|
C | G | 1 | a0001c0001t0005g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1147+11654C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013007 | ||||||
| chr20:45013298
|
A | T | 60 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1148-11675A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013298 | ||||||
| chr20:45013442
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1148-11531A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013442 | ||||||
| chr20:45013724
|
G | C | 1 | a0001c0001t0005g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1148-11249G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013724 | ||||||
| chr20:45013724
|
G | T | 3 | a0002c0002t0003g0137a0002c0002t0003g0171a0002c0002t0003g0172 | 3 | HG02486.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1148-11249G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013724 | ||||||
| chr20:45013878
|
G | A | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1148-11095G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013878 | ||||||
| chr20:45013987
|
T | G | 2 | a0002c0002t0003g0135a0002c0002t0003g0185 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1148-10986T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013987 | ||||||
| chr20:45013988
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0004g0230 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1148-10985A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45013988 | ||||||
| chr20:45014070
|
C | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1148-10903C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014070 | ||||||
| chr20:45014297
|
G | GT | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1148-10675dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45014297 | |||||
| chr20:45014361
|
G | T | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1148-10612G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014361 | ||||||
| chr20:45014473
|
T | C | 154 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1148-10500T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014473 | ||||||
| chr20:45014558
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1148-10415G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014558 | ||||||
| chr20:45014599
|
G | A | 3 | a0002c0002t0003g0137a0002c0002t0003g0171a0002c0002t0003g0172 | 3 | HG02486.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1148-10374G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014599 | ||||||
| chr20:45014841
|
G | T | 1 | a0002c0002t0007g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1148-10132G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45014841 | ||||||
| chr20:45015226
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1148-9747C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015226 | ||||||
| chr20:45015390
|
T | C | 71 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(68): Show | 71 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1148-9583T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015390 | ||||||
| chr20:45015454
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1148-9519A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015454 | ||||||
| chr20:45015518
|
A | G | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1148-9455A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015518 | ||||||
| chr20:45015631
|
A | G | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1148-9342A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015631 | ||||||
| chr20:45015777
|
G | T | 1 | a0001c0001t0005g0066 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1148-9196G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015777 | ||||||
| chr20:45015916
|
A | G | 2 | a0001c0001t0015g0101a0001c0001t0040g0107 | 2 | HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1148-9057A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45015916 | ||||||
| chr20:45016118
|
G | A | 2 | a0002c0002t0003g0138a0002c0002t0003g0146 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1148-8855G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45016118 | ||||||
| chr20:45016237
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1148-8736C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45016237 | ||||||
| chr20:45016398
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1148-8575C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45016398 | ||||||
| chr20:45016723
|
A | G | 14 | a0002c0002t0003g0160a0002c0002t0007g0136a0002c0002t0007g0140others(11): Show | 14 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1148-8250A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45016723 | ||||||
| chr20:45016982
|
A | T | 1 | a0002c0005t0003g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1148-7991A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45016982 | ||||||
| chr20:45017124
|
A | G | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1148-7849A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017124 | ||||||
| chr20:45017153
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179 | 3 | HG01070.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1148-7820A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017153 | ||||||
| chr20:45017409
|
C | T | 1 | a0002c0002t0003g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1148-7564C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017409 | ||||||
| chr20:45017410
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1148-7563G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017410 | ||||||
| chr20:45017529
|
C | T | 154 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1148-7444C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017529 | ||||||
| chr20:45017640
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1148-7333A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017640 | ||||||
| chr20:45017651
|
G | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1148-7322G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017651 | ||||||
| chr20:45017691
|
A | G | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148-7282A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017691 | ||||||
| chr20:45017758
|
G | T | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1148-7215G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45017758 | ||||||
| chr20:45018004
|
T | C | 159 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1148-6969T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018004 | ||||||
| chr20:45018053
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1148-6920A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018053 | ||||||
| chr20:45018151
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1148-6822C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018151 | ||||||
| chr20:45018202
|
AGTTGTTG others(5): Show |
A | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1148-6755_1148-674 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45018202 | |||||
| chr20:45018449
|
A | G | 11 | a0001c0001t0002g0003a0001c0001t0002g0096a0001c0001t0002g0097others(8): Show | 11 | HG00597.hp1 HG02129.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1148-6524A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018449 | ||||||
| chr20:45018574
|
A | T | 1 | a0001c0001t0004g0321 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1148-6399A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018574 | ||||||
| chr20:45018582
|
T | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(58): Show | 61 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1148-6391T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018582 | ||||||
| chr20:45018620
|
G | A | 184 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(181): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1148-6353G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018620 | ||||||
| chr20:45018627
|
T | C | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1148-6346T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018627 | ||||||
| chr20:45018725
|
C | CT | 56 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(53): Show | 56 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1148-6231dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45018725 | |||||
| chr20:45018725
|
CT | C | 18 | a0001c0001t0001g0051a0001c0001t0004g0261a0001c0001t0004g0325others(15): Show | 18 | HG01081.hp1 HG02027.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1148-6231delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45018725 | |||||
| chr20:45018742
|
T | TA | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148-6229dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45018742 | |||||
| chr20:45018989
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-5984C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45018989 | ||||||
| chr20:45019044
|
T | C | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1148-5929T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019044 | ||||||
| chr20:45019049
|
A | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0004g0323 | 3 | HG03490.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1148-5924A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019049 | ||||||
| chr20:45019074
|
G | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-5899G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019074 | ||||||
| chr20:45019101
|
T | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(58): Show | 61 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1148-5872T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019101 | ||||||
| chr20:45019533
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1148-5440A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019533 | ||||||
| chr20:45019613
|
G | T | 14 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0276others(11): Show | 14 | HG01496.hp2 HG01952.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.1148-5360G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019613 | ||||||
| chr20:45019817
|
T | C | 23 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0138others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1148-5156T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019817 | ||||||
| chr20:45019892
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1148-5081T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019892 | ||||||
| chr20:45019901
|
C | T | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1148-5072C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019901 | ||||||
| chr20:45019972
|
T | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1148-5001T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45019972 | ||||||
| chr20:45020090
|
T | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1148-4883T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020090 | ||||||
| chr20:45020231
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-4742A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020231 | ||||||
| chr20:45020281
|
ATGCAGTT others(6): Show |
A | 2 | a0001c0001t0001g0227a0001c0001t0004g0230 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1148-4678_1148-466 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020281 | |||||
| chr20:45020285
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1148-4688A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020285 | ||||||
| chr20:45020420
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1148-4553T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020420 | ||||||
| chr20:45020439
|
CGT | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0227others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1148-4507_1148-450 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020439 | |||||
| chr20:45020458
|
GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1148-4513_1148-450 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020458 | |||||
| chr20:45020460
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0006g0189 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1148-4511_1148-450 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020460 | |||||
| chr20:45020462
|
GTGTGTAT others(3): Show |
G | 89 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(86): Show | 89 | HG00423.hp2 HG00597.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.1148-4509_1148-450 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020462 | |||||
| chr20:45020462
|
GTGTGTAT others(9): Show |
G | 1 | a0001c0001t0005g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1148-4509_1148-449 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020462 | |||||
| chr20:45020464
|
GTGTA | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0033a0002c0002t0007g0136others(2): Show | 5 | HG01168.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148-4505_1148-450 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020464 | |||||
| chr20:45020464
|
GTGTATGT others(1): Show |
G | 63 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0037others(60): Show | 63 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1148-4507_1148-450 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020464 | |||||
| chr20:45020464
|
GTGTATGT others(3): Show |
G | 7 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(4): Show | 7 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148-4505_1148-449 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020464 | |||||
| chr20:45020466
|
GTATGTT | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1148-4477_1148-447 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020466 | |||||
| chr20:45020466
|
GTATGTTT others(5): Show |
G | 3 | a0001c0001t0018g0049a0001c0001t0018g0050a0001c0001t0035g0045 | 3 | HG02886.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1148-4483_1148-447 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020466 | |||||
| chr20:45020468
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1148-4505A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020468 | ||||||
| chr20:45020472
|
T | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0011g0085others(3): Show | 6 | HG01168.hp2 HG01361.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-4501T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020472 | ||||||
| chr20:45020474
|
A | G | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1148-4499A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020474 | ||||||
| chr20:45020478
|
T | G | 8 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(5): Show | 8 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148-4495T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020478 | ||||||
| chr20:45020480
|
A | G | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1148-4493A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020480 | ||||||
| chr20:45020486
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1148-4487A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020486 | ||||||
| chr20:45020543
|
A | G | 1 | a0001c0001t0016g0192 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1148-4430A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020543 | ||||||
| chr20:45020816
|
CT | C | 60 | a0001c0001t0001g0051a0001c0001t0011g0085a0001c0001t0012g0044others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1148-4144delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45020816 | |||||
| chr20:45020821
|
T | C | 7 | a0001c0001t0001g0317a0001c0001t0004g0005a0001c0001t0004g0315others(4): Show | 7 | HG00423.hp1 HG00621.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148-4152T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020821 | ||||||
| chr20:45020862
|
A | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1148-4111A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020862 | ||||||
| chr20:45020945
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1148-4028G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020945 | ||||||
| chr20:45020959
|
G | A | 4 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082others(1): Show | 4 | HG01167.hp1 HG01243.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148-4014G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020959 | ||||||
| chr20:45020985
|
T | A | 1 | a0002c0002t0003g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1148-3988T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45020985 | ||||||
| chr20:45021039
|
C | G | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1148-3934C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021039 | ||||||
| chr20:45021061
|
C | A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1148-3912C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021061 | ||||||
| chr20:45021260
|
A | G | 1 | a0001c0001t0008g0214 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1148-3713A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021260 | ||||||
| chr20:45021400
|
G | C | 1 | a0001c0001t0030g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1148-3573G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021400 | ||||||
| chr20:45021460
|
T | C | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1148-3513T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021460 | ||||||
| chr20:45021495
|
T | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1148-3478T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021495 | ||||||
| chr20:45021828
|
A | G | 61 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(58): Show | 61 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1148-3145A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45021828 | ||||||
| chr20:45022057
|
A | AT | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1148-2907dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45022057 | |||||
| chr20:45022116
|
G | A | 1 | a0001c0001t0005g0066 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1148-2857G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022116 | ||||||
| chr20:45022299
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1148-2674G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022299 | ||||||
| chr20:45022419
|
C | G | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1148-2554C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022419 | ||||||
| chr20:45022533
|
A | AT | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-2439dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45022533 | |||||
| chr20:45022611
|
T | C | 1 | a0002c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1148-2362T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022611 | ||||||
| chr20:45022827
|
A | G | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-2146A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022827 | ||||||
| chr20:45022889
|
T | C | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148-2084T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022889 | ||||||
| chr20:45022940
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1148-2033G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45022940 | ||||||
| chr20:45023089
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-1884G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023089 | ||||||
| chr20:45023247
|
G | A | 1 | a0002c0002t0007g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1148-1726G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023247 | ||||||
| chr20:45023353
|
G | A | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1148-1620G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023353 | ||||||
| chr20:45023486
|
G | A | 305 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1148-1487G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023486 | ||||||
| chr20:45023675
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1148-1298T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023675 | ||||||
| chr20:45023680
|
T | C | 1 | a0002c0002t0003g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1148-1293T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023680 | ||||||
| chr20:45023765
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1148-1208C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45023765 | ||||||
| chr20:45023895
|
C | CT | 25 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0037others(22): Show | 25 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1148-1055dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45023895 | |||||
| chr20:45023895
|
CT | C | 13 | a0001c0001t0001g0288a0001c0001t0002g0092a0001c0001t0002g0109others(10): Show | 13 | HG00735.hp1 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1148-1055delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45023895 | |||||
| chr20:45023895
|
CTT | C | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-1056_1148-105 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45023895 | |||||
| chr20:45024001
|
C | T | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148-972C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024001 | ||||||
| chr20:45024049
|
C | T | 29 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(26): Show | 29 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1148-924C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024049 | ||||||
| chr20:45024077
|
T | C | 1 | a0002c0005t0003g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1148-896T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024077 | ||||||
| chr20:45024086
|
G | A | 8 | a0001c0001t0009g0202a0001c0001t0009g0204a0001c0001t0009g0205others(5): Show | 8 | HG00621.hp1 NA18946.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1148-887G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024086 | ||||||
| chr20:45024190
|
G | A | 2 | a0001c0001t0008g0223a0001c0001t0008g0225 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1148-783G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024190 | ||||||
| chr20:45024195
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1148-778T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024195 | ||||||
| chr20:45024244
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1148-729A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024244 | ||||||
| chr20:45024304
|
G | GT | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1148-657dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 45024304 | |||||
| chr20:45024366
|
T | A | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1148-607T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024366 | ||||||
| chr20:45024410
|
A | T | 1 | a0001c0001t0001g0029 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1148-563A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024410 | ||||||
| chr20:45024771
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1148-202C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024771 | ||||||
| chr20:45024904
|
T | C | 1 | a0002c0002t0003g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1148-69T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 9/10 | chr20 | 45024904 | ||||||
| chr20:45025169
|
G | A | 3 | a0002c0002t0007g0156a0002c0002t0007g0168a0002c0002t0007g0169 | 3 | HG01517.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1305+39G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025169 | ||||||
| chr20:45025217
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+87A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025217 | ||||||
| chr20:45025330
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1305+200G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025330 | ||||||
| chr20:45025435
|
G | A | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1305+305G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025435 | ||||||
| chr20:45025530
|
C | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1305+400C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025530 | ||||||
| chr20:45025899
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179 | 3 | HG01070.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1305+769C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025899 | ||||||
| chr20:45025933
|
G | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1305+803G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45025933 | ||||||
| chr20:45026082
|
C | T | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+952C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026082 | ||||||
| chr20:45026083
|
T | TC | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+953_1305+954i others(3): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026083 | ||||||
| chr20:45026128
|
G | GGTTTTTT others(4): Show |
6 | a0001c0001t0012g0044a0001c0001t0012g0047a0001c0001t0012g0048others(3): Show | 6 | HG01081.hp1 HG02886.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+998_1305+999i others(13): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026128 | ||||||
| chr20:45026128
|
G | GGTTTTTT others(5): Show |
4 | a0001c0001t0001g0051a0001c0001t0012g0046a0001c0001t0012g0053others(1): Show | 4 | HG02027.hp1 HG02698.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+998_1305+999i others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026128 | ||||||
| chr20:45026128
|
G | GT | 86 | a0001c0001t0001g0035a0001c0001t0002g0003a0001c0001t0002g0043others(83): Show | 86 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1305+1015dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026128 | |||||
| chr20:45026128
|
GT | G | 46 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1305+1015delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026128 | |||||
| chr20:45026318
|
A | AGT | 26 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0227others(23): Show | 26 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1305+1218_1305+121 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
A | AGTGT | 9 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0002g0087others(6): Show | 9 | HG01074.hp2 HG01243.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+1216_1305+121 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
A | AGTGTGT | 34 | a0001c0001t0005g0002a0001c0001t0005g0055a0001c0001t0005g0056others(31): Show | 34 | HG00741.hp1 HG01106.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1305+1214_1305+121 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
A | AGTGTGTG others(1): Show |
25 | a0001c0001t0005g0058a0001c0001t0005g0060a0001c0001t0005g0062others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1305+1212_1305+121 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
A | AGTGTGTG others(3): Show |
25 | a0001c0001t0038g0220a0002c0002t0003g0135a0002c0002t0003g0139others(22): Show | 25 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1305+1210_1305+121 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
A | AGTGTGTG others(7): Show |
5 | a0001c0001t0008g0223a0001c0001t0008g0224a0001c0001t0008g0225others(2): Show | 5 | HG00639.hp2 HG01261.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+1206_1305+121 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
AGT | A | 27 | a0001c0001t0001g0275a0001c0001t0003g0228a0001c0001t0006g0186others(24): Show | 27 | HG00621.hp1 HG02083.hp1 HG02809.hp1 others(24): Show |
intron_variant | MODIFIER | c.1305+1218_1305+121 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
AGTGT | A | 16 | a0001c0001t0001g0317a0001c0001t0004g0005a0001c0001t0004g0231others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1305+1216_1305+121 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026318
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0002g0096a0001c0001t0002g0118 | 2 | NA18990.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1305+1210_1305+121 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45026318 | |||||
| chr20:45026394
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+1264T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026394 | ||||||
| chr20:45026494
|
A | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+1364A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026494 | ||||||
| chr20:45026765
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+1635A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026765 | ||||||
| chr20:45026806
|
A | G | 1 | a0001c0001t0030g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1305+1676A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026806 | ||||||
| chr20:45026834
|
C | T | 1 | a0002c0002t0003g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1305+1704C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026834 | ||||||
| chr20:45026861
|
A | G | 1 | a0002c0002t0003g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1305+1731A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026861 | ||||||
| chr20:45026962
|
A | G | 1 | a0001c0001t0008g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1305+1832A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45026962 | ||||||
| chr20:45027116
|
G | T | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+1986G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027116 | ||||||
| chr20:45027124
|
A | G | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1305+1994A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027124 | ||||||
| chr20:45027141
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+2011G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027141 | ||||||
| chr20:45027166
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 46 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.1305+2036C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027166 | ||||||
| chr20:45027201
|
G | A | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+2071G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027201 | ||||||
| chr20:45027206
|
A | G | 2 | a0001c0001t0012g0053a0001c0001t0034g0052 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1305+2076A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027206 | ||||||
| chr20:45027223
|
G | C | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1305+2093G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027223 | ||||||
| chr20:45027283
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2153C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027283 | ||||||
| chr20:45027290
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2160T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027290 | ||||||
| chr20:45027293
|
G | T | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2163G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027293 | ||||||
| chr20:45027297
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2167G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027297 | ||||||
| chr20:45027298
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2168T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027298 | ||||||
| chr20:45027299
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2169G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027299 | ||||||
| chr20:45027301
|
A | T | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2171A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027301 | ||||||
| chr20:45027306
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1305+2176T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027306 | ||||||
| chr20:45027379
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1305+2249G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027379 | ||||||
| chr20:45027423
|
T | G | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1305+2293T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027423 | ||||||
| chr20:45027430
|
C | CA | 39 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179others(36): Show | 39 | HG00423.hp1 HG00621.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1305+2320dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45027430 | |||||
| chr20:45027430
|
CA | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0174others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1305+2320delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45027430 | |||||
| chr20:45027687
|
T | C | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1305+2557T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027687 | ||||||
| chr20:45027724
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+2594A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027724 | ||||||
| chr20:45027792
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1305+2662G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027792 | ||||||
| chr20:45027824
|
T | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+2694T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027824 | ||||||
| chr20:45027915
|
A | G | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+2785A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45027915 | ||||||
| chr20:45028065
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1305+2935A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028065 | ||||||
| chr20:45028083
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+2953A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028083 | ||||||
| chr20:45028110
|
T | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+2980T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028110 | ||||||
| chr20:45028252
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+3122T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028252 | ||||||
| chr20:45028327
|
CT | C | 20 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0001g0288others(17): Show | 20 | HG01167.hp1 HG01256.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1305+3212delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45028327 | |||||
| chr20:45028430
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+3300A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028430 | ||||||
| chr20:45028629
|
T | A | 3 | a0002c0002t0003g0137a0002c0002t0003g0171a0002c0002t0003g0172 | 3 | HG02486.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1305+3499T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028629 | ||||||
| chr20:45028639
|
G | A | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+3509G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028639 | ||||||
| chr20:45028724
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+3594C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028724 | ||||||
| chr20:45028780
|
G | A | 3 | a0001c0001t0001g0267a0001c0001t0028g0268a0002c0002t0003g0151 | 3 | HG04228.hp1 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1305+3650G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028780 | ||||||
| chr20:45028804
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+3674C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028804 | ||||||
| chr20:45028869
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+3739G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45028869 | ||||||
| chr20:45029026
|
A | G | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1305+3896A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029026 | ||||||
| chr20:45029160
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1305+4030T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029160 | ||||||
| chr20:45029327
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1305+4197T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029327 | ||||||
| chr20:45029375
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+4245C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029375 | ||||||
| chr20:45029398
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+4268A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029398 | ||||||
| chr20:45029647
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0025 | 2 | HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+4517A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029647 | ||||||
| chr20:45029651
|
C | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+4521C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029651 | ||||||
| chr20:45029696
|
A | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+4566A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029696 | ||||||
| chr20:45029958
|
A | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+4828A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029958 | ||||||
| chr20:45029972
|
T | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+4842T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45029972 | ||||||
| chr20:45030019
|
C | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1305+4889C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030019 | ||||||
| chr20:45030034
|
A | C | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+4904A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030034 | ||||||
| chr20:45030107
|
C | CT | 59 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1305+4991dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45030107 | |||||
| chr20:45030107
|
CT | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+4991delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45030107 | |||||
| chr20:45030192
|
T | C | 159 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1305+5062T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030192 | ||||||
| chr20:45030318
|
C | A | 1 | a0001c0001t0004g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1305+5188C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030318 | ||||||
| chr20:45030347
|
ACT | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+5222_1305+522 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45030347 | |||||
| chr20:45030610
|
G | A | 3 | a0002c0002t0007g0156a0002c0002t0007g0168a0002c0002t0007g0169 | 3 | HG01517.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1305+5480G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030610 | ||||||
| chr20:45030654
|
C | A | 2 | a0001c0001t0004g0261a0001c0001t0004g0262 | 2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1305+5524C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030654 | ||||||
| chr20:45030695
|
T | C | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1305+5565T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030695 | ||||||
| chr20:45030724
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1305+5594A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030724 | ||||||
| chr20:45030787
|
T | C | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+5657T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45030787 | ||||||
| chr20:45031048
|
A | C | 4 | a0001c0001t0004g0313a0001c0001t0004g0314a0001c0001t0004g0324others(1): Show | 4 | HG00438.hp2 NA18993.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+5918A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031048 | ||||||
| chr20:45031174
|
AT | A | 126 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0002g0003others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1305+6058delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45031174 | |||||
| chr20:45031294
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+6164T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031294 | ||||||
| chr20:45031365
|
C | T | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1305+6235C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031365 | ||||||
| chr20:45031530
|
C | T | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1305+6400C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031530 | ||||||
| chr20:45031553
|
G | A | 1 | a0001c0001t0006g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1305+6423G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031553 | ||||||
| chr20:45031554
|
G | T | 1 | a0001c0001t0006g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1305+6424G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031554 | ||||||
| chr20:45031593
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+6463G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031593 | ||||||
| chr20:45031733
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+6603C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031733 | ||||||
| chr20:45031753
|
A | G | 10 | a0002c0002t0003g0138a0002c0002t0003g0144a0002c0002t0003g0146others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1305+6623A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031753 | ||||||
| chr20:45031860
|
A | G | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+6730A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031860 | ||||||
| chr20:45031882
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+6752C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031882 | ||||||
| chr20:45031885
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+6755A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031885 | ||||||
| chr20:45031891
|
C | T | 23 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0138others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1305+6761C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45031891 | ||||||
| chr20:45031904
|
C | CA | 61 | a0001c0001t0001g0030a0001c0001t0001g0227a0001c0001t0002g0124others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1305+6795dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45031904 | |||||
| chr20:45031904
|
C | CAA | 36 | a0001c0001t0001g0051a0001c0001t0005g0002a0001c0001t0005g0042others(33): Show | 36 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1305+6794_1305+679 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45031904 | |||||
| chr20:45031904
|
CA | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0234a0001c0001t0001g0282others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+6795delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45031904 | |||||
| chr20:45032175
|
A | G | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1305+7045A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032175 | ||||||
| chr20:45032268
|
C | CT | 48 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1305+7146dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45032268 | |||||
| chr20:45032348
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1305+7218G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032348 | ||||||
| chr20:45032414
|
C | G | 1 | a0001c0001t0029g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1305+7284C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032414 | ||||||
| chr20:45032415
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179 | 3 | HG01070.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1305+7285C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032415 | ||||||
| chr20:45032842
|
C | T | 1 | a0001c0001t0005g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1305+7712C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032842 | ||||||
| chr20:45032896
|
A | G | 2 | a0001c0001t0008g0221a0001c0001t0037g0222 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1305+7766A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032896 | ||||||
| chr20:45032947
|
T | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1305+7817T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032947 | ||||||
| chr20:45032983
|
A | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+7853A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45032983 | ||||||
| chr20:45033072
|
T | C | 1 | a0001c0001t0005g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1305+7942T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45033072 | ||||||
| chr20:45033574
|
GT | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+8452delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45033574 | |||||
| chr20:45033599
|
CAG | C | 7 | a0001c0001t0001g0317a0001c0001t0004g0005a0001c0001t0004g0315others(4): Show | 7 | HG00423.hp1 HG00621.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+8472_1305+847 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45033599 | |||||
| chr20:45033622
|
G | T | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1305+8492G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45033622 | ||||||
| chr20:45033690
|
C | T | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1305+8560C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45033690 | ||||||
| chr20:45033695
|
T | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+8565T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45033695 | ||||||
| chr20:45033851
|
A | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+8721A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45033851 | ||||||
| chr20:45034066
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+8936A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034066 | ||||||
| chr20:45034138
|
G | T | 4 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9008G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034138 | ||||||
| chr20:45034485
|
C | T | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1305+9355C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034485 | ||||||
| chr20:45034545
|
G | T | 1 | a0001c0001t0019g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1305+9415G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034545 | ||||||
| chr20:45034612
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+9482G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034612 | ||||||
| chr20:45034627
|
CA | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+9498delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034627 | ||||||
| chr20:45034669
|
TGGGAGGT others(6): Show |
T | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9546_1305+955 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45034669 | |||||
| chr20:45034682
|
C | T | 1 | a0001c0001t0012g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1305+9552C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034682 | ||||||
| chr20:45034743
|
T | C | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9613T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034743 | ||||||
| chr20:45034756
|
A | G | 9 | a0001c0001t0002g0091a0001c0001t0002g0103a0001c0001t0002g0104others(6): Show | 9 | NA18947.hp1 NA18965.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1305+9626A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034756 | ||||||
| chr20:45034868
|
G | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+9738G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034868 | ||||||
| chr20:45034869
|
A | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+9739A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034869 | ||||||
| chr20:45034937
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1305+9807A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45034937 | ||||||
| chr20:45035245
|
T | C | 1 | a0001c0001t0004g0005 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1305+10115T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035245 | ||||||
| chr20:45035286
|
A | G | 3 | a0001c0001t0008g0221a0001c0001t0037g0222a0001c0001t0038g0220 | 3 | HG01884.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1305+10156A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035286 | ||||||
| chr20:45035402
|
C | T | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+10272C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035402 | ||||||
| chr20:45035421
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1305+10291T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035421 | ||||||
| chr20:45035446
|
G | A | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1305+10316G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035446 | ||||||
| chr20:45035615
|
T | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+10485T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035615 | ||||||
| chr20:45035823
|
AG | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+10694delG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035823 | ||||||
| chr20:45035925
|
T | C | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+10795T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45035925 | ||||||
| chr20:45035983
|
T | TA | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 47 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1305+10860dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45035983 | |||||
| chr20:45036011
|
T | A | 1 | a0001c0001t0001g0278 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1305+10881T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036011 | ||||||
| chr20:45036029
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0033 | 2 | NA18983.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1305+10899T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036029 | ||||||
| chr20:45036197
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1305+11067G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036197 | ||||||
| chr20:45036339
|
G | A | 1 | a0001c0001t0009g0209 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1305+11209G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036339 | ||||||
| chr20:45036349
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+11219G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036349 | ||||||
| chr20:45036650
|
C | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+11520C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036650 | ||||||
| chr20:45036727
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+11597A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45036727 | ||||||
| chr20:45037191
|
G | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1305+12061G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037191 | ||||||
| chr20:45037404
|
A | AT | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+12280dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45037404 | |||||
| chr20:45037438
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+12308G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037438 | ||||||
| chr20:45037510
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+12380A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037510 | ||||||
| chr20:45037594
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+12464A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037594 | ||||||
| chr20:45037664
|
G | A | 1 | a0001c0001t0008g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1305+12534G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037664 | ||||||
| chr20:45037754
|
G | A | 3 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0194 | 3 | NA18966.hp2 NA18985.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1305+12624G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45037754 | ||||||
| chr20:45038073
|
G | A | 5 | a0001c0001t0004g0310a0001c0001t0004g0313a0001c0001t0004g0314others(2): Show | 5 | HG00438.hp2 NA18942.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+12943G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038073 | ||||||
| chr20:45038320
|
A | AAAATAT | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+13192_1305+13 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45038320 | |||||
| chr20:45038320
|
A | AAATTAT | 143 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1305+13194_1305+13 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45038320 | |||||
| chr20:45038331
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1305+13201C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038331 | ||||||
| chr20:45038378
|
C | CA | 4 | a0001c0001t0005g0060a0001c0001t0005g0061a0001c0001t0005g0062others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+13254dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45038378 | |||||
| chr20:45038457
|
T | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1305+13327T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038457 | ||||||
| chr20:45038466
|
A | T | 24 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(21): Show | 24 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(21): Show |
intron_variant | MODIFIER | c.1305+13336A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038466 | ||||||
| chr20:45038499
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+13369T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038499 | ||||||
| chr20:45038691
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+13561G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038691 | ||||||
| chr20:45038964
|
A | C | 14 | a0002c0002t0003g0160a0002c0002t0007g0136a0002c0002t0007g0140others(11): Show | 14 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1305+13834A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45038964 | ||||||
| chr20:45039135
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1305+14005A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039135 | ||||||
| chr20:45039290
|
A | G | 61 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(58): Show | 61 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1305+14160A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039290 | ||||||
| chr20:45039418
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+14288C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039418 | ||||||
| chr20:45039625
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+14495A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039625 | ||||||
| chr20:45039736
|
A | G | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+14606A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039736 | ||||||
| chr20:45039832
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1305+14702G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45039832 | ||||||
| chr20:45040045
|
AT | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1305+14932delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45040045 | |||||
| chr20:45040045
|
ATT | A | 12 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(9): Show | 12 | HG00735.hp1 HG01081.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+14931_1305+14 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45040045 | |||||
| chr20:45040115
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1305+14985A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040115 | ||||||
| chr20:45040285
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1305+15155T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040285 | ||||||
| chr20:45040446
|
T | A | 159 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1305+15316T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040446 | ||||||
| chr20:45040550
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1305+15420G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040550 | ||||||
| chr20:45040571
|
A | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+15441A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040571 | ||||||
| chr20:45040633
|
CT | C | 46 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1305+15517delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45040633 | |||||
| chr20:45040657
|
A | C | 1 | a0001c0001t0011g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1305+15527A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040657 | ||||||
| chr20:45040829
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1305+15699T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040829 | ||||||
| chr20:45040959
|
G | A | 154 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1305+15829G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45040959 | ||||||
| chr20:45041000
|
T | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1305+15870T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041000 | ||||||
| chr20:45041077
|
A | T | 3 | a0001c0001t0019g0177a0001c0001t0019g0178a0001c0001t0044g0176 | 3 | HG01891.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1305+15947A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041077 | ||||||
| chr20:45041079
|
A | G | 1 | a0001c0001t0008g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1305+15949A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041079 | ||||||
| chr20:45041099
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+15969A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041099 | ||||||
| chr20:45041138
|
G | GT | 4 | a0001c0001t0005g0060a0001c0001t0005g0061a0001c0001t0005g0062others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+16014dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45041138 | |||||
| chr20:45041160
|
T | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+16030T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041160 | ||||||
| chr20:45041324
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1305+16194C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041324 | ||||||
| chr20:45041326
|
CACAG | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+16200_1305+16 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45041326 | |||||
| chr20:45041380
|
T | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+16250T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041380 | ||||||
| chr20:45041597
|
G | T | 54 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(51): Show | 54 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1305+16467G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45041597 | ||||||
| chr20:45041685
|
CT | C | 144 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0002g0003others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1305+16569delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45041685 | |||||
| chr20:45042058
|
G | A | 4 | a0001c0001t0014g0256a0001c0001t0014g0257a0001c0001t0014g0258others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+16928G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042058 | ||||||
| chr20:45042061
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0028g0268 | 2 | NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1305+16931G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042061 | ||||||
| chr20:45042215
|
C | CTCT | 123 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1305+17090_1305+17 others(9): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042215 | |||||
| chr20:45042233
|
G | A | 156 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1305+17103G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042233 | ||||||
| chr20:45042274
|
G | GT | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+17153dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042274 | |||||
| chr20:45042290
|
C | T | 4 | a0001c0001t0005g0060a0001c0001t0005g0061a0001c0001t0005g0062others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+17160C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042290 | ||||||
| chr20:45042482
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0026 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1305+17352G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042482 | ||||||
| chr20:45042572
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+17442G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042572 | ||||||
| chr20:45042579
|
G | T | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1305+17449G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042579 | ||||||
| chr20:45042710
|
T | C | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1305+17580T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042710 | ||||||
| chr20:45042751
|
G | A | 1 | a0002c0002t0003g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1305+17621G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042751 | ||||||
| chr20:45042765
|
AAC | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1305+17639_1305+17 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042765 | |||||
| chr20:45042791
|
G | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+17661G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042791 | ||||||
| chr20:45042804
|
T | G | 1 | a0002c0002t0007g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1305+17674T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042804 | ||||||
| chr20:45042878
|
G | GCAGGATG others(322): Show |
5 | a0001c0001t0012g0053a0001c0001t0018g0049a0001c0001t0018g0050others(2): Show | 5 | HG02886.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+17758_1305+17 others(335): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042878 | |||||
| chr20:45042878
|
G | GCAGGATG others(324): Show |
1 | a0001c0001t0012g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1305+17758_1305+17 others(337): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042878 | |||||
| chr20:45042878
|
G | GCAGGATG others(325): Show |
4 | a0001c0001t0001g0051a0001c0001t0012g0046a0001c0001t0012g0047others(1): Show | 4 | HG02027.hp1 HG02698.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+17758_1305+17 others(338): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042878 | |||||
| chr20:45042878
|
G | GCAGGATG others(340): Show |
1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1305+17758_1305+17 others(353): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45042878 | |||||
| chr20:45042889
|
T | A | 161 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1305+17759T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45042889 | ||||||
| chr20:45043122
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1305+17992G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043122 | ||||||
| chr20:45043164
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1305+18034T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043164 | ||||||
| chr20:45043174
|
G | A | 1 | a0001c0001t0044g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1305+18044G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043174 | ||||||
| chr20:45043623
|
A | G | 123 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1305+18493A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043623 | ||||||
| chr20:45043643
|
A | T | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1305+18513A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043643 | ||||||
| chr20:45043764
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(3): Show | 6 | HG01952.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+18634A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043764 | ||||||
| chr20:45043857
|
A | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+18727A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043857 | ||||||
| chr20:45043894
|
A | G | 3 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088 | 3 | HG01074.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1305+18764A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043894 | ||||||
| chr20:45043902
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+18772C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043902 | ||||||
| chr20:45043951
|
T | C | 2 | a0001c0001t0005g0059a0001c0001t0005g0065 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1305+18821T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45043951 | ||||||
| chr20:45044072
|
A | G | 161 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1305+18942A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044072 | ||||||
| chr20:45044087
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1305+18957A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044087 | ||||||
| chr20:45044164
|
A | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+19034A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044164 | ||||||
| chr20:45044248
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1305+19118C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044248 | ||||||
| chr20:45044269
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0088 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1305+19139C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044269 | ||||||
| chr20:45044512
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+19382G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044512 | ||||||
| chr20:45044604
|
G | A | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+19474G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044604 | ||||||
| chr20:45044678
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1305+19548A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044678 | ||||||
| chr20:45044789
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1305+19659G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044789 | ||||||
| chr20:45044858
|
A | G | 1 | a0001c0001t0004g0321 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1305+19728A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45044858 | ||||||
| chr20:45045051
|
C | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0088 | 3 | HG01074.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1305+19921C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045051 | ||||||
| chr20:45045208
|
A | G | 1 | a0001c0001t0017g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1305+20078A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045208 | ||||||
| chr20:45045307
|
A | T | 4 | a0001c0001t0014g0256a0001c0001t0014g0257a0001c0001t0014g0258others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+20177A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045307 | ||||||
| chr20:45045440
|
A | G | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1305+20310A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045440 | ||||||
| chr20:45045516
|
A | G | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1305+20386A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045516 | ||||||
| chr20:45045523
|
A | G | 34 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(31): Show | 34 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1305+20393A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045523 | ||||||
| chr20:45045545
|
A | G | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+20415A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045545 | ||||||
| chr20:45045562
|
T | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1305+20432T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045562 | ||||||
| chr20:45045794
|
CT | C | 184 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(181): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1305+20674delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45045794 | |||||
| chr20:45045942
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+20812C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045942 | ||||||
| chr20:45045945
|
TACAGGTG others(16): Show |
T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+20816_1305+20 others(29): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45045945 | ||||||
| chr20:45046007
|
A | G | 1 | a0002c0002t0003g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1305+20877A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046007 | ||||||
| chr20:45046059
|
C | T | 2 | a0001c0001t0004g0326a0002c0002t0043g0084 | 2 | HG02723.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1305+20929C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046059 | ||||||
| chr20:45046088
|
T | A | 1 | a0002c0002t0003g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1305+20958T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046088 | ||||||
| chr20:45046265
|
C | CA | 12 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(9): Show | 12 | HG01081.hp1 HG02027.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1305+21149dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45046265 | |||||
| chr20:45046265
|
CA | C | 55 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1305+21149delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45046265 | |||||
| chr20:45046446
|
GA | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+21330delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45046446 | |||||
| chr20:45046455
|
A | G | 3 | a0001c0001t0018g0049a0001c0001t0018g0050a0001c0001t0035g0045 | 3 | HG02886.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1305+21325A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046455 | ||||||
| chr20:45046675
|
A | T | 8 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305+21545A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046675 | ||||||
| chr20:45046689
|
A | T | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+21559A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046689 | ||||||
| chr20:45046701
|
A | G | 1 | a0001c0001t0005g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1305+21571A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046701 | ||||||
| chr20:45046743
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1305+21613G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046743 | ||||||
| chr20:45046751
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1305+21621G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046751 | ||||||
| chr20:45046755
|
C | G | 1 | a0002c0002t0007g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1305+21625C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046755 | ||||||
| chr20:45046915
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1305+21785C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046915 | ||||||
| chr20:45046926
|
C | T | 12 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(9): Show | 12 | HG01358.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+21796C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046926 | ||||||
| chr20:45046927
|
G | A | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+21797G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046927 | ||||||
| chr20:45046967
|
A | G | 1 | a0003c0003t0001g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1305+21837A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45046967 | ||||||
| chr20:45047038
|
G | A | 3 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0194 | 3 | NA18966.hp2 NA18985.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1305+21908G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047038 | ||||||
| chr20:45047267
|
G | A | 2 | a0001c0001t0005g0002a0001c0001t0005g0076 | 2 | HG01358.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1305+22137G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047267 | ||||||
| chr20:45047391
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+22261C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047391 | ||||||
| chr20:45047511
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+22381G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047511 | ||||||
| chr20:45047535
|
T | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+22405T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047535 | ||||||
| chr20:45047717
|
G | A | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1305+22587G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047717 | ||||||
| chr20:45047726
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0033 | 2 | NA18983.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1305+22596A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047726 | ||||||
| chr20:45047771
|
T | C | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+22641T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047771 | ||||||
| chr20:45047932
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+22802C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047932 | ||||||
| chr20:45047940
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1305+22810G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047940 | ||||||
| chr20:45047974
|
T | A | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1305+22844T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45047974 | ||||||
| chr20:45048074
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+22944C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048074 | ||||||
| chr20:45048381
|
T | C | 1 | a0001c0001t0032g0009 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1305+23251T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048381 | ||||||
| chr20:45048425
|
C | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+23295C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048425 | ||||||
| chr20:45048645
|
C | A | 1 | a0001c0001t0030g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1305+23515C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048645 | ||||||
| chr20:45048667
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1305+23537A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048667 | ||||||
| chr20:45048670
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+23540C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048670 | ||||||
| chr20:45048728
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+23598C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048728 | ||||||
| chr20:45048966
|
A | G | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1305+23836A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45048966 | ||||||
| chr20:45048994
|
G | GT | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+23874dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45048994 | |||||
| chr20:45049143
|
A | T | 154 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1305+24013A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45049143 | ||||||
| chr20:45049600
|
T | A | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1305+24470T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45049600 | ||||||
| chr20:45049642
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 38 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1305+24512T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45049642 | ||||||
| chr20:45049687
|
A | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+24557A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45049687 | ||||||
| chr20:45049804
|
C | T | 1 | a0001c0001t0017g0032 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1305+24674C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45049804 | ||||||
| chr20:45050181
|
G | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-24837G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050181 | ||||||
| chr20:45050485
|
C | A | 2 | a0002c0002t0003g0171a0002c0002t0003g0172 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1306-24533C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050485 | ||||||
| chr20:45050603
|
C | T | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-24415C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050603 | ||||||
| chr20:45050720
|
T | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-24298T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050720 | ||||||
| chr20:45050758
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-24260A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050758 | ||||||
| chr20:45050823
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1306-24195A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45050823 | ||||||
| chr20:45051380
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-23638T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051380 | ||||||
| chr20:45051502
|
G | A | 2 | a0001c0001t0005g0074a0001c0001t0005g0077 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1306-23516G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051502 | ||||||
| chr20:45051503
|
G | C | 5 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-23515G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051503 | ||||||
| chr20:45051567
|
G | C | 1 | a0001c0001t0005g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1306-23451G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051567 | ||||||
| chr20:45051630
|
T | C | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-23388T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051630 | ||||||
| chr20:45051801
|
A | C | 1 | a0001c0001t0011g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1306-23217A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051801 | ||||||
| chr20:45051922
|
T | C | 1 | a0001c0001t0037g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306-23096T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45051922 | ||||||
| chr20:45052174
|
A | G | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1306-22844A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052174 | ||||||
| chr20:45052175
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-22843A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052175 | ||||||
| chr20:45052197
|
G | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-22821G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052197 | ||||||
| chr20:45052202
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | NA18969.hp1 NA19072.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1306-22816A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052202 | ||||||
| chr20:45052277
|
AC | A | 148 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1306-22733delC | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45052277 | |||||
| chr20:45052301
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 38 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1306-22717A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052301 | ||||||
| chr20:45052461
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1306-22557A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052461 | ||||||
| chr20:45052775
|
G | A | 4 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-22243G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052775 | ||||||
| chr20:45052839
|
C | A | 6 | a0001c0001t0008g0221a0001c0001t0008g0223a0001c0001t0008g0224others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-22179C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052839 | ||||||
| chr20:45052922
|
T | C | 115 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1306-22096T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052922 | ||||||
| chr20:45052947
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1306-22071A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45052947 | ||||||
| chr20:45053310
|
C | T | 117 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1306-21708C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053310 | ||||||
| chr20:45053483
|
A | G | 186 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(183): Show | 186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1306-21535A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053483 | ||||||
| chr20:45053599
|
A | G | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-21419A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053599 | ||||||
| chr20:45053612
|
G | C | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-21406G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053612 | ||||||
| chr20:45053720
|
T | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-21298T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053720 | ||||||
| chr20:45053756
|
C | T | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1306-21262C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053756 | ||||||
| chr20:45053770
|
A | G | 13 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(10): Show | 13 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306-21248A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053770 | ||||||
| chr20:45053910
|
T | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-21108T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053910 | ||||||
| chr20:45053919
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0018 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1306-21099T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45053919 | ||||||
| chr20:45053919
|
T | TC | 14 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(11): Show | 14 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306-21098dupC | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45053919 | |||||
| chr20:45054129
|
C | T | 1 | a0001c0001t0005g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1306-20889C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054129 | ||||||
| chr20:45054130
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-20888G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054130 | ||||||
| chr20:45054158
|
C | T | 46 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1306-20860C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054158 | ||||||
| chr20:45054181
|
C | T | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-20837C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054181 | ||||||
| chr20:45054348
|
G | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-20670G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054348 | ||||||
| chr20:45054487
|
C | CA | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-20531_1306-20 others(7): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054487 | ||||||
| chr20:45054523
|
C | T | 12 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(9): Show | 12 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306-20495C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054523 | ||||||
| chr20:45054553
|
C | A | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-20465C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054553 | ||||||
| chr20:45054559
|
C | CT | 7 | a0001c0001t0001g0039a0001c0001t0001g0239a0001c0001t0001g0290others(4): Show | 7 | HG01099.hp1 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1306-20441dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45054559 | |||||
| chr20:45054559
|
CT | C | 39 | a0001c0001t0001g0051a0001c0001t0001g0288a0001c0001t0005g0057others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1306-20441delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45054559 | |||||
| chr20:45054598
|
A | G | 25 | a0001c0001t0001g0008a0001c0001t0001g0267a0001c0001t0001g0269others(22): Show | 25 | HG00438.hp1 HG01496.hp2 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-20420A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054598 | ||||||
| chr20:45054608
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-20410C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054608 | ||||||
| chr20:45054656
|
G | A | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1306-20362G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054656 | ||||||
| chr20:45054759
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0018 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1306-20259A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45054759 | ||||||
| chr20:45055065
|
C | T | 2 | a0001c0001t0002g0102a0001c0001t0002g0109 | 2 | NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1306-19953C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055065 | ||||||
| chr20:45055193
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1306-19825C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055193 | ||||||
| chr20:45055201
|
C | G | 1 | a0001c0001t0013g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1306-19817C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055201 | ||||||
| chr20:45055324
|
A | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(318): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1306-19694A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055324 | ||||||
| chr20:45055645
|
GTTTA | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-19369_1306-19 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45055645 | |||||
| chr20:45055673
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-19345A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055673 | ||||||
| chr20:45055725
|
CTTTT | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-19286_1306-19 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45055725 | |||||
| chr20:45055798
|
T | C | 1 | a0001c0001t0012g0046 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1306-19220T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055798 | ||||||
| chr20:45055820
|
C | T | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-19198C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055820 | ||||||
| chr20:45055828
|
G | A | 54 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(51): Show | 54 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1306-19190G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055828 | ||||||
| chr20:45055828
|
G | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-19190G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055828 | ||||||
| chr20:45055880
|
A | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-19138A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055880 | ||||||
| chr20:45055982
|
C | T | 1 | a0001c0001t0006g0198 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1306-19036C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45055982 | ||||||
| chr20:45056020
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-18998C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056020 | ||||||
| chr20:45056022
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-18996C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056022 | ||||||
| chr20:45056023
|
G | A | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-18995G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056023 | ||||||
| chr20:45056042
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-18976C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056042 | ||||||
| chr20:45056184
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-18834A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056184 | ||||||
| chr20:45056201
|
GT | G | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-18813delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45056201 | |||||
| chr20:45056282
|
A | C | 2 | a0002c0002t0003g0135a0002c0002t0003g0185 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1306-18736A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056282 | ||||||
| chr20:45056490
|
A | G | 1 | a0001c0001t0004g0312 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1306-18528A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056490 | ||||||
| chr20:45056743
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-18275G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056743 | ||||||
| chr20:45056869
|
T | C | 123 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1306-18149T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056869 | ||||||
| chr20:45056901
|
A | C | 1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306-18117A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056901 | ||||||
| chr20:45056908
|
A | T | 1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306-18110A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056908 | ||||||
| chr20:45056915
|
T | C | 2 | a0001c0001t0019g0177a0001c0001t0019g0178 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1306-18103T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056915 | ||||||
| chr20:45056921
|
T | A | 1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306-18097T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056921 | ||||||
| chr20:45056922
|
T | TCAAAGTT others(4): Show |
1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306-18096_1306-18 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45056922 | ||||||
| chr20:45056962
|
GTCGTTTA others(3): Show |
G | 1 | a0001c0001t0004g0326 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306-18053_1306-18 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45056962 | |||||
| chr20:45057019
|
T | C | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-17999T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057019 | ||||||
| chr20:45057022
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1306-17996G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057022 | ||||||
| chr20:45057213
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-17805C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057213 | ||||||
| chr20:45057354
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1306-17664T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057354 | ||||||
| chr20:45057369
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-17649A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057369 | ||||||
| chr20:45057409
|
T | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02027.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1306-17609T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057409 | ||||||
| chr20:45057474
|
G | A | 1 | a0002c0002t0007g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1306-17544G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057474 | ||||||
| chr20:45057520
|
C | T | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1306-17498C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057520 | ||||||
| chr20:45057692
|
G | A | 1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1306-17326G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057692 | ||||||
| chr20:45057905
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1306-17113G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45057905 | ||||||
| chr20:45058003
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1306-17015A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058003 | ||||||
| chr20:45058013
|
A | G | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-17005A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058013 | ||||||
| chr20:45058053
|
TCA | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(162): Show | 166 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1306-16931_1306-16 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058053 | |||||
| chr20:45058053
|
TCACA | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0087a0001c0001t0002g0089others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-16933_1306-16 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058053 | |||||
| chr20:45058053
|
TCACACA | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1306-16935_1306-16 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058053 | |||||
| chr20:45058053
|
TCACACAC others(1): Show |
T | 28 | a0001c0001t0001g0051a0001c0001t0002g0091a0001c0001t0002g0092others(25): Show | 28 | HG01081.hp1 HG01361.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1306-16937_1306-16 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058053 | |||||
| chr20:45058053
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-16941_1306-16 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058053 | |||||
| chr20:45058093
|
A | C | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306-16925A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058093 | ||||||
| chr20:45058154
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1306-16864A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058154 | ||||||
| chr20:45058214
|
A | AT | 12 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(9): Show | 12 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306-16793dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45058214 | |||||
| chr20:45058652
|
G | A | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-16366G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058652 | ||||||
| chr20:45058665
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(2): Show | 5 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-16353C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058665 | ||||||
| chr20:45058714
|
C | G | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306-16304C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058714 | ||||||
| chr20:45058818
|
G | A | 3 | a0002c0002t0007g0156a0002c0002t0007g0168a0002c0002t0007g0169 | 3 | HG01517.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1306-16200G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058818 | ||||||
| chr20:45058868
|
G | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0232 | 3 | HG03490.hp1 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1306-16150G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45058868 | ||||||
| chr20:45059035
|
T | A | 5 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(2): Show | 5 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-15983T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059035 | ||||||
| chr20:45059065
|
T | C | 156 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1306-15953T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059065 | ||||||
| chr20:45059091
|
A | G | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-15927A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059091 | ||||||
| chr20:45059511
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-15507A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059511 | ||||||
| chr20:45059756
|
T | C | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1306-15262T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059756 | ||||||
| chr20:45059761
|
A | G | 1 | a0001c0001t0025g0226 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1306-15257A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059761 | ||||||
| chr20:45059775
|
A | G | 1 | a0001c0001t0004g0312 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1306-15243A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059775 | ||||||
| chr20:45059776
|
A | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306-15242A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059776 | ||||||
| chr20:45059794
|
C | T | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-15224C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45059794 | ||||||
| chr20:45060136
|
G | A | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-14882G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060136 | ||||||
| chr20:45060233
|
A | G | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306-14785A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060233 | ||||||
| chr20:45060302
|
G | A | 3 | a0001c0001t0002g0097a0001c0001t0002g0123a0001c0001t0002g0124 | 3 | HG00597.hp1 HG02155.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1306-14716G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060302 | ||||||
| chr20:45060373
|
C | A | 1 | a0001c0001t0030g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1306-14645C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060373 | ||||||
| chr20:45060412
|
G | A | 1 | a0001c0001t0009g0209 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1306-14606G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060412 | ||||||
| chr20:45060456
|
A | T | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1306-14562A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060456 | ||||||
| chr20:45060457
|
GT | G | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-14553delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45060457 | |||||
| chr20:45060560
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0022 | 2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1306-14458C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060560 | ||||||
| chr20:45060567
|
G | T | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-14451G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060567 | ||||||
| chr20:45060733
|
T | G | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-14285T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45060733 | ||||||
| chr20:45061085
|
T | C | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-13933T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061085 | ||||||
| chr20:45061134
|
A | AAAAAC | 5 | a0001c0001t0001g0281a0001c0001t0019g0177a0001c0001t0019g0178others(2): Show | 5 | HG01891.hp1 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-13867_1306-13 others(11): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061134 | |||||
| chr20:45061157
|
G | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-13861G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061157 | ||||||
| chr20:45061180
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1306-13838G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061180 | ||||||
| chr20:45061188
|
G | A | 161 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1306-13830G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061188 | ||||||
| chr20:45061192
|
C | T | 1 | a0001c0001t0006g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1306-13826C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061192 | ||||||
| chr20:45061235
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0223others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-13783C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061235 | ||||||
| chr20:45061237
|
A | C | 1 | a0001c0001t0001g0007 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1306-13781A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061237 | ||||||
| chr20:45061360
|
A | G | 2 | a0002c0002t0003g0171a0002c0002t0003g0172 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1306-13658A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061360 | ||||||
| chr20:45061393
|
T | C | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-13625T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061393 | ||||||
| chr20:45061397
|
C | A | 1 | a0001c0001t0011g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1306-13621C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061397 | ||||||
| chr20:45061398
|
G | A | 11 | a0001c0001t0002g0003a0001c0001t0002g0096a0001c0001t0002g0097others(8): Show | 11 | HG00597.hp1 HG02129.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306-13620G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061398 | ||||||
| chr20:45061562
|
C | G | 161 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1306-13456C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061562 | ||||||
| chr20:45061596
|
A | AT | 87 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0002g0003others(84): Show | 87 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1306-13405dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061596 | |||||
| chr20:45061596
|
A | ATT | 44 | a0001c0001t0001g0051a0001c0001t0002g0119a0001c0001t0011g0085others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1306-13406_1306-13 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061596 | |||||
| chr20:45061596
|
A | ATTT | 15 | a0002c0002t0003g0154a0002c0002t0003g0160a0002c0002t0007g0136others(12): Show | 15 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1306-13407_1306-13 others(9): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061596 | |||||
| chr20:45061638
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1306-13380G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061638 | ||||||
| chr20:45061806
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0004g0286 | 2 | HG03927.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1306-13212G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061806 | ||||||
| chr20:45061872
|
C | CT | 16 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0248others(13): Show | 16 | HG00735.hp1 HG02698.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306-13125dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061872 | |||||
| chr20:45061872
|
CT | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0174a0001c0001t0001g0281others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306-13125delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061872 | |||||
| chr20:45061872
|
CTTTTTT | C | 33 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(30): Show | 33 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306-13130_1306-13 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45061872 | |||||
| chr20:45061875
|
T | C | 3 | a0001c0001t0008g0221a0001c0001t0037g0222a0001c0001t0038g0220 | 3 | HG01884.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1306-13143T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061875 | ||||||
| chr20:45061918
|
C | T | 14 | a0002c0002t0003g0160a0002c0002t0007g0136a0002c0002t0007g0140others(11): Show | 14 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1306-13100C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061918 | ||||||
| chr20:45061920
|
C | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-13098C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061920 | ||||||
| chr20:45061930
|
A | C | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1306-13088A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061930 | ||||||
| chr20:45061943
|
G | A | 1 | a0001c0001t0005g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1306-13075G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061943 | ||||||
| chr20:45061984
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-13034A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45061984 | ||||||
| chr20:45062173
|
C | G | 4 | a0001c0001t0009g0204a0001c0001t0009g0205a0001c0001t0009g0206others(1): Show | 4 | NA18973.hp2 NA18980.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-12845C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062173 | ||||||
| chr20:45062200
|
C | A | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-12818C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062200 | ||||||
| chr20:45062268
|
T | G | 1 | a0001c0001t0006g0198 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1306-12750T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062268 | ||||||
| chr20:45062310
|
C | T | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-12708C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062310 | ||||||
| chr20:45062457
|
TG | T | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-12558delG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062457 | |||||
| chr20:45062460
|
G | C | 11 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-12558G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062460 | ||||||
| chr20:45062468
|
G | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-12550G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062468 | ||||||
| chr20:45062555
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1306-12463G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062555 | ||||||
| chr20:45062589
|
G | A | 45 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1306-12429G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062589 | ||||||
| chr20:45062608
|
G | A | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-12410G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062608 | ||||||
| chr20:45062738
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-12280C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062738 | ||||||
| chr20:45062740
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0002g0114a0001c0001t0012g0044others(8): Show | 11 | HG01081.hp1 HG02027.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306-12278C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062740 | ||||||
| chr20:45062763
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179others(1): Show | 4 | HG01070.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-12255C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062763 | ||||||
| chr20:45062823
|
G | A | 69 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(66): Show | 69 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1306-12195G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062823 | ||||||
| chr20:45062835
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1306-12183G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062835 | ||||||
| chr20:45062843
|
A | AT | 43 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0241others(40): Show | 43 | HG00621.hp1 HG01106.hp2 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.1306-12155dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062843 | |||||
| chr20:45062843
|
AT | A | 70 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0227others(67): Show | 70 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1306-12155delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062843 | |||||
| chr20:45062932
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1306-12086C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062932 | ||||||
| chr20:45062936
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1306-12082C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062936 | ||||||
| chr20:45062942
|
G | A | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-12076G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062942 | ||||||
| chr20:45062983
|
C | T | 13 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(10): Show | 13 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306-12035C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45062983 | ||||||
| chr20:45062989
|
C | CT | 27 | a0001c0001t0001g0054a0001c0001t0001g0233a0001c0001t0001g0241others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1306-11999dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTT | 9 | a0001c0001t0001g0037a0001c0001t0001g0239a0001c0001t0001g0246others(6): Show | 9 | HG00280.hp2 HG00621.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-12000_1306-11 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT | 6 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(3): Show | 6 | HG02300.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-12005_1306-11 others(13): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0005g0060a0001c0001t0005g0063a0001c0001t0008g0214others(5): Show | 8 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306-12006_1306-11 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0005g0062a0001c0001t0005g0067a0001c0001t0012g0048others(8): Show | 11 | HG00323.hp1 HG00323.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-12007_1306-11 others(15): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(3): Show |
30 | a0001c0001t0002g0099a0001c0001t0002g0109a0001c0001t0002g0123others(27): Show | 30 | HG00280.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1306-12008_1306-11 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(4): Show |
20 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0090others(17): Show | 20 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1306-12009_1306-11 others(17): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0002g0088a0001c0001t0002g0097a0001c0001t0002g0098others(4): Show | 7 | HG00597.hp1 HG01258.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306-12010_1306-11 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0094a0001c0001t0002g0102 | 2 | NA18966.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1306-12011_1306-11 others(19): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0066 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1306-12012_1306-11 others(20): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0110a0001c0001t0005g0064 | 2 | HG00423.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1306-12013_1306-11 others(21): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0089 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1306-12014_1306-11 others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0002g0087a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 4 | HG01074.hp2 HG01891.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-12015_1306-11 others(23): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1306-12016_1306-11 others(24): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0095 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1306-12017_1306-11 others(25): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0005g0071a0001c0001t0021g0070 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1306-12021_1306-11 others(29): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(17): Show |
5 | a0001c0001t0001g0227a0001c0001t0002g0091a0001c0001t0002g0121others(2): Show | 5 | HG02055.hp1 HG02135.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-12022_1306-11 others(30): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0002g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1306-12023_1306-11 others(31): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1306-12024_1306-11 others(32): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1306-12027_1306-11 others(35): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(23): Show |
2 | a0002c0002t0003g0137a0002c0002t0007g0165 | 2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1306-12028_1306-11 others(36): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0015g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-11999_1306-11 others(38): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0002g0093 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1306-11999_1306-11 others(39): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0115 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1306-11999_1306-11 others(40): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0002g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1306-11999_1306-11 others(41): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
C | CTTTTTTT others(37): Show |
1 | a0001c0001t0005g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1306-11999_1306-11 others(50): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
CT | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(61): Show | 65 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1306-11999delT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01358.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-12008_1306-11 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0276 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1306-12010_1306-11 others(18): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0043g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1306-12011_1306-11 others(19): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45062989
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | NA18969.hp1 NA19072.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-12014_1306-11 others(22): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45062989 | |||||
| chr20:45063043
|
A | G | 2 | a0001c0001t0015g0101a0001c0001t0040g0107 | 2 | HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1306-11975A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063043 | ||||||
| chr20:45063078
|
A | ACTG | 11 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306-11938_1306-11 others(9): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45063078 | |||||
| chr20:45063296
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1306-11722C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063296 | ||||||
| chr20:45063343
|
G | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1306-11675G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063343 | ||||||
| chr20:45063385
|
T | C | 159 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1306-11633T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063385 | ||||||
| chr20:45063783
|
A | AG | 25 | a0001c0001t0001g0302a0001c0001t0002g0003a0001c0001t0002g0091others(22): Show | 25 | HG00597.hp1 HG02074.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-11227dupG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45063783 | |||||
| chr20:45063790
|
G | T | 2 | a0001c0001t0011g0085a0001c0001t0039g0127 | 2 | HG01361.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1306-11228G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063790 | ||||||
| chr20:45063838
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-11180C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063838 | ||||||
| chr20:45063875
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1306-11143T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063875 | ||||||
| chr20:45063992
|
G | T | 121 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1306-11026G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45063992 | ||||||
| chr20:45064043
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-10975C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064043 | ||||||
| chr20:45064100
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1306-10918G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064100 | ||||||
| chr20:45064109
|
A | AG | 40 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306-10900dupG | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45064109 | |||||
| chr20:45064112
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1306-10906G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064112 | ||||||
| chr20:45064113
|
G | T | 1 | a0001c0001t0001g0277 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1306-10905G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064113 | ||||||
| chr20:45064263
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1306-10755G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064263 | ||||||
| chr20:45064378
|
G | GT | 8 | a0001c0001t0001g0012a0001c0001t0004g0318a0001c0001t0011g0129others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306-10630dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45064378 | |||||
| chr20:45064647
|
C | T | 14 | a0001c0001t0005g0059a0001c0001t0005g0064a0001c0001t0005g0065others(11): Show | 14 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306-10371C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064647 | ||||||
| chr20:45064703
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1306-10315T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064703 | ||||||
| chr20:45064921
|
C | A | 1 | a0001c0001t0004g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1306-10097C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45064921 | ||||||
| chr20:45065026
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1306-9992G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065026 | ||||||
| chr20:45065050
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1306-9968T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065050 | ||||||
| chr20:45065095
|
G | T | 3 | a0001c0001t0008g0221a0001c0001t0037g0222a0001c0001t0038g0220 | 3 | HG01884.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1306-9923G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065095 | ||||||
| chr20:45065141
|
G | GT | 50 | a0001c0001t0011g0085a0001c0001t0012g0086a0001c0001t0031g0301others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.1306-9865dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45065141 | |||||
| chr20:45065343
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-9675C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065343 | ||||||
| chr20:45065433
|
G | A | 3 | a0001c0001t0008g0223a0001c0001t0008g0224a0001c0001t0008g0225 | 3 | HG01261.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1306-9585G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065433 | ||||||
| chr20:45065630
|
C | CT | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-9388_1306-938 others(5): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065630 | ||||||
| chr20:45065631
|
A | T | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-9387A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065631 | ||||||
| chr20:45065636
|
G | A | 1 | a0002c0002t0003g0135 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1306-9382G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065636 | ||||||
| chr20:45065804
|
A | T | 6 | a0001c0001t0008g0211a0001c0001t0008g0212a0001c0001t0008g0213others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-9214A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065804 | ||||||
| chr20:45065835
|
A | G | 1 | a0002c0002t0003g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1306-9183A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065835 | ||||||
| chr20:45065897
|
T | C | 1 | a0001c0001t0035g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1306-9121T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45065897 | ||||||
| chr20:45066007
|
A | T | 22 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0138others(19): Show | 22 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1306-9011A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066007 | ||||||
| chr20:45066181
|
T | TAC | 15 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(12): Show | 15 | HG02040.hp1 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1306-8805_1306-880 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
T | TACAC | 25 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0265others(22): Show | 26 | HG00280.hp2 HG00597.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.1306-8807_1306-880 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
T | TACACAC | 53 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0278others(50): Show | 53 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.1306-8809_1306-880 others(10): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
T | TACACACA others(1): Show |
10 | a0001c0001t0008g0221a0001c0001t0010g0252a0001c0001t0011g0129others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-8811_1306-880 others(12): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
T | TACACACA others(3): Show |
9 | a0001c0001t0001g0227a0001c0001t0008g0223a0001c0001t0008g0224others(6): Show | 9 | HG01081.hp1 HG01261.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1306-8813_1306-880 others(14): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
T | TACACACA others(5): Show |
1 | a0001c0001t0033g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1306-8815_1306-880 others(16): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
TAC | T | 41 | a0001c0001t0001g0014a0001c0001t0001g0302a0001c0001t0005g0059others(38): Show | 41 | HG00621.hp1 HG01106.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.1306-8805_1306-880 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066181
|
TACAC | T | 61 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1306-8807_1306-880 others(8): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45066181 | |||||
| chr20:45066297
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1306-8721A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066297 | ||||||
| chr20:45066403
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1306-8615A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066403 | ||||||
| chr20:45066508
|
C | G | 1 | a0001c0001t0004g0264 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1306-8510C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066508 | ||||||
| chr20:45066535
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1306-8483C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066535 | ||||||
| chr20:45066762
|
A | G | 13 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(10): Show | 13 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306-8256A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066762 | ||||||
| chr20:45066802
|
A | G | 46 | a0002c0002t0003g0134a0002c0002t0003g0135a0002c0002t0003g0137others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1306-8216A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066802 | ||||||
| chr20:45066904
|
C | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-8114C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45066904 | ||||||
| chr20:45067078
|
C | T | 3 | a0001c0001t0008g0223a0001c0001t0008g0224a0001c0001t0008g0225 | 3 | HG01261.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1306-7940C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067078 | ||||||
| chr20:45067121
|
T | C | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-7897T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067121 | ||||||
| chr20:45067161
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0284a0001c0001t0001g0292others(1): Show | 5 | HG02083.hp2 HG02165.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-7857G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067161 | ||||||
| chr20:45067227
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0253 | 2 | HG02602.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1306-7791G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067227 | ||||||
| chr20:45067303
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0232 | 3 | HG03490.hp1 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1306-7715C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067303 | ||||||
| chr20:45067544
|
G | A | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1306-7474G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067544 | ||||||
| chr20:45067662
|
A | G | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-7356A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067662 | ||||||
| chr20:45067667
|
C | G | 1 | a0002c0002t0003g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1306-7351C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067667 | ||||||
| chr20:45067815
|
A | T | 116 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0002g0003others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1306-7203A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067815 | ||||||
| chr20:45067848
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0290 | 3 | HG02027.hp2 NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1306-7170G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067848 | ||||||
| chr20:45067942
|
G | A | 14 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306-7076G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067942 | ||||||
| chr20:45067967
|
C | T | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-7051C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45067967 | ||||||
| chr20:45068307
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0088 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1306-6711C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45068307 | ||||||
| chr20:45068313
|
T | C | 13 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0008g0211others(10): Show | 13 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306-6705T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45068313 | ||||||
| chr20:45069087
|
G | A | 49 | a0001c0001t0011g0085a0001c0001t0039g0127a0002c0002t0003g0134others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-5931G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069087 | ||||||
| chr20:45069221
|
A | G | 2 | a0001c0001t0019g0177a0001c0001t0019g0178 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1306-5797A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069221 | ||||||
| chr20:45069380
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-5638A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069380 | ||||||
| chr20:45069447
|
C | G | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-5571C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069447 | ||||||
| chr20:45069531
|
T | G | 116 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0002g0003others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1306-5487T>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069531 | ||||||
| chr20:45069652
|
C | T | 1 | a0001c0001t0004g0312 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1306-5366C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069652 | ||||||
| chr20:45069710
|
A | T | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1306-5308A>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069710 | ||||||
| chr20:45069866
|
G | T | 1 | a0001c0001t0015g0112 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1306-5152G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45069866 | ||||||
| chr20:45070396
|
A | G | 1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1306-4622A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070396 | ||||||
| chr20:45070402
|
T | C | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-4616T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070402 | ||||||
| chr20:45070444
|
G | A | 4 | a0002c0002t0003g0180a0002c0002t0003g0181a0002c0002t0003g0182others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-4574G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070444 | ||||||
| chr20:45070528
|
G | A | 1 | a0001c0001t0004g0005 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306-4490G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070528 | ||||||
| chr20:45070587
|
G | A | 68 | a0001c0001t0001g0037a0001c0001t0001g0227a0001c0001t0002g0003others(65): Show | 68 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1306-4431G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070587 | ||||||
| chr20:45070595
|
C | T | 9 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(6): Show | 9 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-4423C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070595 | ||||||
| chr20:45070630
|
A | C | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-4388A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070630 | ||||||
| chr20:45070826
|
T | C | 1 | a0002c0002t0003g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306-4192T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45070826 | ||||||
| chr20:45070885
|
C | CA | 97 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0054others(94): Show | 97 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1306-4114dupA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45070885 | |||||
| chr20:45070885
|
C | CAA | 7 | a0001c0001t0002g0093a0001c0001t0002g0096a0001c0001t0002g0098others(4): Show | 7 | HG03927.hp1 NA18939.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306-4115_1306-411 others(6): Show |
STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45070885 | |||||
| chr20:45070885
|
CA | C | 68 | a0001c0001t0001g0233a0001c0001t0003g0228a0001c0001t0004g0230others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1306-4114delA | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45070885 | |||||
| chr20:45071050
|
G | T | 1 | a0001c0001t0006g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1306-3968G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071050 | ||||||
| chr20:45071118
|
G | A | 2 | a0002c0002t0003g0144a0002c0002t0003g0152 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1306-3900G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071118 | ||||||
| chr20:45071380
|
A | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0131others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-3638A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071380 | ||||||
| chr20:45071444
|
T | C | 1 | a0001c0001t0024g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1306-3574T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071444 | ||||||
| chr20:45071520
|
A | G | 1 | a0002c0002t0003g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1306-3498A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071520 | ||||||
| chr20:45071664
|
G | C | 14 | a0002c0002t0003g0160a0002c0002t0007g0136a0002c0002t0007g0140others(11): Show | 14 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1306-3354G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071664 | ||||||
| chr20:45071707
|
T | C | 10 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-3311T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071707 | ||||||
| chr20:45071792
|
A | G | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-3226A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071792 | ||||||
| chr20:45071906
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1306-3112T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071906 | ||||||
| chr20:45071940
|
T | A | 1 | a0001c0001t0001g0253 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1306-3078T>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071940 | ||||||
| chr20:45071946
|
G | A | 1 | a0002c0002t0011g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1306-3072G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45071946 | ||||||
| chr20:45072054
|
T | C | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-2964T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072054 | ||||||
| chr20:45072184
|
A | G | 3 | a0001c0001t0014g0256a0001c0001t0014g0257a0001c0001t0014g0258 | 3 | HG02647.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1306-2834A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072184 | ||||||
| chr20:45072246
|
G | C | 154 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1306-2772G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072246 | ||||||
| chr20:45072285
|
G | A | 9 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(6): Show | 9 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-2733G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072285 | ||||||
| chr20:45072430
|
A | G | 1 | a0001c0001t0012g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1306-2588A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072430 | ||||||
| chr20:45072475
|
A | G | 1 | a0001c0001t0005g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1306-2543A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072475 | ||||||
| chr20:45072714
|
T | C | 9 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(6): Show | 9 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-2304T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072714 | ||||||
| chr20:45072971
|
C | T | 1 | a0001c0001t0035g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1306-2047C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072971 | ||||||
| chr20:45072986
|
A | G | 10 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-2032A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45072986 | ||||||
| chr20:45073021
|
G | A | 9 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(6): Show | 9 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-1997G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073021 | ||||||
| chr20:45073030
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1306-1988G>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073030 | ||||||
| chr20:45073130
|
T | C | 2 | a0001c0001t0015g0101a0001c0001t0040g0107 | 2 | HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1306-1888T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073130 | ||||||
| chr20:45073176
|
A | G | 10 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(7): Show | 10 | HG01081.hp1 HG02027.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-1842A>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073176 | ||||||
| chr20:45073259
|
A | AT | 6 | a0001c0001t0004g0297a0001c0001t0004g0310a0001c0001t0004g0313others(3): Show | 6 | HG00438.hp1 HG00438.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-1749dupT | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 45073259 | |||||
| chr20:45073275
|
C | G | 1 | a0001c0001t0042g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1306-1743C>G | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073275 | ||||||
| chr20:45073277
|
A | C | 1 | a0001c0001t0005g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1306-1741A>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073277 | ||||||
| chr20:45073336
|
C | T | 4 | a0001c0001t0002g0090a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-1682C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073336 | ||||||
| chr20:45073476
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1306-1542G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073476 | ||||||
| chr20:45073546
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0175a0001c0001t0001g0179others(1): Show | 4 | HG01070.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-1472G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073546 | ||||||
| chr20:45073790
|
T | C | 154 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1306-1228T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073790 | ||||||
| chr20:45073870
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-1148G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073870 | ||||||
| chr20:45073903
|
C | A | 1 | a0001c0001t0001g0269 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1306-1115C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45073903 | ||||||
| chr20:45074506
|
G | A | 2 | a0001c0001t0010g0242a0001c0001t0010g0254 | 2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1306-512G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074506 | ||||||
| chr20:45074526
|
G | A | 1 | a0001c0001t0039g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-492G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074526 | ||||||
| chr20:45074554
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0087others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1306-464C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074554 | ||||||
| chr20:45074564
|
G | T | 30 | a0001c0001t0005g0002a0001c0001t0005g0041a0001c0001t0005g0042others(27): Show | 30 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1306-454G>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074564 | ||||||
| chr20:45074607
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1306-411C>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074607 | ||||||
| chr20:45074790
|
T | C | 1 | a0001c0001t0004g0321 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1306-228T>C | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074790 | ||||||
| chr20:45074886
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1306-132C>T | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074886 | ||||||
| chr20:45074990
|
G | A | 25 | a0001c0001t0006g0186a0001c0001t0006g0187a0001c0001t0006g0188others(22): Show | 25 | HG00621.hp1 HG02083.hp1 NA18612.hp1 others(22): Show |
intron_variant | MODIFIER | c.1306-28G>A | STK4 | ENSG00000101109.13 | transcript | ENST00000372806.8 | protein_coding | 10/10 | chr20 | 45074990 |