Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23012 |
|---|---|
| ensemblid | ENSG00000211455.8 |
| hgncid | 17848 |
| symbol | STK38L |
| name | serine/threonine kinase 38 like |
| refseq_nuc | NM_015000.4 |
| refseq_prot | NP_055815.1 |
| ensembl_nuc | ENST00000389032.8 |
| ensembl_prot | ENSP00000373684.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27244286 |
| end | 27325959 |
| strand | + |
| ver | v1.2 |
| region | chr12:27244286-27325959 |
| region5000 | chr12:27239286-27330959 |
| regionname0 | STK38L_chr12_27244286_27325959 |
| regionname5000 | STK38L_chr12_27239286_27330959 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 464 | 374 | 86 | 64 | 178 | 8 | 36 | 144 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| 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 | 0/1 | 1395 | 354 | 73 | 60 | 178 | 8 | 34 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| c0002 | 0/0 | 1395 | 13 | 12 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| c0003 | 1/0 | 1395 | 7 | 1 | 3 | 0 | 0 | 2 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3565 | 115 | 22 | 31 | 50 | 3 | 9 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0002 | 0/0 | 3565 | 91 | 15 | 9 | 57 | 1 | 9 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0003 | 0/0 | 3565 | 72 | 2 | 5 | 58 | 0 | 7 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0004 | 1/0 | 3563 | 43 | 6 | 15 | 9 | 4 | 8 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0005 | 0/0 | 3565 | 18 | 17 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0006 | 0/1 | 3565 | 12 | 6 | 2 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0007 | 0/0 | 3565 | 6 | 6 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0008 | 0/0 | 3565 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0009 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0010 | 0/0 | 3563 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0011 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0012 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0013 | 0/0 | 3565 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0014 | 0/0 | 3565 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0015 | 0/0 | 3565 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0016 | 0/0 | 3565 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0017 | 0/0 | 3565 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| t0018 | 0/0 | 3565 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| 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 | 0/1 | 1395 | 354 | 73 | 60 | 178 | 8 | 34 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0002 | 0/0 | 1395 | 13 | 12 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0003 | 1/0 | 1395 | 7 | 1 | 3 | 0 | 0 | 2 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4959 | 114 | 21 | 31 | 50 | 3 | 9 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0002 | 0/0 | 4959 | 85 | 14 | 6 | 57 | 1 | 7 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0003 | 0/0 | 4959 | 72 | 2 | 5 | 58 | 0 | 7 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0004 | 0/0 | 4957 | 42 | 6 | 15 | 9 | 4 | 8 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0005 | 0/0 | 4959 | 6 | 6 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0006 | 0/1 | 4959 | 12 | 6 | 2 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0007 | 0/0 | 4959 | 6 | 6 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0008 | 0/0 | 4959 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0009 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0010 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0011 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0012 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0013 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0014 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0015 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0016 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0017 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0001t0018 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0002t0001 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0002t0005 | 0/0 | 4959 | 12 | 11 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0003t0002 | 0/0 | 4959 | 6 | 1 | 3 | 0 | 0 | 2 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| a0001c0003t0004 | 1/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | copy fasta | chr12 | 27239286 | 27330959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0010g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0012g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0012g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0014g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0016g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0017g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0001t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0002t0005g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| a0001c0003t0004g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0256 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0268 | EUR | GBR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0255 | EUR | FIN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | FIN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | CHS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0119 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00741 | hp1 | a0001 | c0002 | t0005 | g0356 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0346 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0345 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0344 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0253 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01361 | hp1 | a0001 | c0001 | t0017 | g0276 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0103 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0266 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0117 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0260 | EUR | IBS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0291 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0234 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0309 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0355 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0352 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0041 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0357 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0339 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0328 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0120 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0176 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0337 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0043 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0351 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0354 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0108 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0350 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0236 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0341 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0237 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0100 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0004 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0349 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0102 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0118 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0353 | AFR | ESN | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0293 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0348 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0124 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0264 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0114 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0342 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0269 | SAS | STU | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0231 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0004 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18946 | hp1 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0070 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0295 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | LWK | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19058 | hp1 | a0001 | c0001 | t0016 | g0048 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19078 | hp1 | a0001 | c0001 | t0010 | g0332 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0235 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0004 | AFR | YRI | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ASW | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ASW | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | GIH | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | GIH | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0343 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0014 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0347 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0338 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | USA | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0170 | REF | REF | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0004 | g0252 | REF | REF | STK38L_chr12_27239286_27330959 | STK38L | chr12 | 27239286 | 27330959 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27297738
|
G | T | 1 | a0001c0002 | 13 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.18G>T | p.Gly6Gly | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/14 | 76/4957 | 18/1395 | 6/464 | chr12 | 27297738 | ||
| chr12:27317933
|
G | A | 2 | a0001c0001a0001c0002 | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.993G>A | p.Thr331Thr | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/14 | 1051/4957 | 993/1395 | 331/464 | chr12 | 27317933 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27297714
|
C | T | 1 | a0001c0001t0018 | 1 | HG03209.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/14 | chr12 | 27297714 | ||||||
| chr12:27322519
|
C | T | 1 | a0001c0001t0007 | 6 | HG01891.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*64C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 64 | chr12 | 27322519 | |||||
| chr12:27322788
|
A | G | 2 | a0001c0001t0006a0001c0001t0008 | 15 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 333 | chr12 | 27322788 | |||||
| chr12:27323025
|
T | C | 1 | a0001c0001t0009 | 2 | HG01891.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*570T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 570 | chr12 | 27323025 | |||||
| chr12:27323201
|
T | G | 1 | a0001c0001t0010 | 2 | NA18946.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*746T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 746 | chr12 | 27323201 | |||||
| chr12:27323612
|
A | G | 5 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(2): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1157A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1157 | chr12 | 27323612 | |||||
| chr12:27324166
|
A | T | 1 | a0001c0001t0016 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1711A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1711 | chr12 | 27324166 | |||||
| chr12:27324174
|
C | T | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 132 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1719 | chr12 | 27324174 | |||||
| chr12:27324249
|
A | ACT | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | 329 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*1795_*1796dupCT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 1797 | INFO_REALIGN_3_PRIME | chr12 | 27324249 | ||||
| chr12:27324564
|
G | A | 1 | a0001c0001t0011 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2109G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2109 | chr12 | 27324564 | |||||
| chr12:27324702
|
T | G | 2 | a0001c0001t0005a0001c0002t0005 | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2247T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2247 | chr12 | 27324702 | |||||
| chr12:27324814
|
G | A | 1 | a0001c0001t0012 | 2 | HG02258.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2359G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2359 | chr12 | 27324814 | |||||
| chr12:27324866
|
A | G | 1 | a0001c0001t0013 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2411 | chr12 | 27324866 | |||||
| chr12:27325051
|
T | C | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2596T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2596 | chr12 | 27325051 | |||||
| chr12:27325060
|
T | C | 1 | a0001c0001t0017 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2605T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 2605 | chr12 | 27325060 | |||||
| chr12:27325928
|
G | C | 1 | a0001c0001t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3473G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 14/14 | 3473 | chr12 | 27325928 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27244406
|
A | T | 24 | a0001c0001t0001g0340a0001c0001t0004g0013a0001c0001t0004g0336others(21): Show | 27 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12+74A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244406 | ||||||
| chr12:27244433
|
G | A | 1 | a0001c0003t0002g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+101G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244433 | ||||||
| chr12:27244456
|
C | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0335a0001c0001t0004g0333others(2): Show | 6 | HG00609.hp2 NA19007.hp2 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+124C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244456 | ||||||
| chr12:27244540
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0008g0331 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+208A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244540 | ||||||
| chr12:27244589
|
C | A | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+257C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244589 | ||||||
| chr12:27244859
|
T | C | 225 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(222): Show | 235 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.-12+527T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27244859 | ||||||
| chr12:27245015
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-12+683G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245015 | ||||||
| chr12:27245196
|
G | A | 15 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+864G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245196 | ||||||
| chr12:27245313
|
C | T | 73 | a0001c0001t0001g0224a0001c0001t0001g0233a0001c0001t0002g0001others(70): Show | 75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-12+981C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245313 | ||||||
| chr12:27245545
|
A | C | 251 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(248): Show | 264 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.-12+1213A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245545 | ||||||
| chr12:27245676
|
C | A | 1 | a0001c0001t0006g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12+1344C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245676 | ||||||
| chr12:27245774
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-12+1442A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27245774 | ||||||
| chr12:27246018
|
A | G | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+1686A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246018 | ||||||
| chr12:27246070
|
A | G | 327 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(324): Show | 342 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.-12+1738A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246070 | ||||||
| chr12:27246224
|
G | A | 1 | a0001c0003t0002g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+1892G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246224 | ||||||
| chr12:27246311
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-12+1979A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246311 | ||||||
| chr12:27246328
|
T | TTG | 327 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(324): Show | 342 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.-12+2007_-12+2008d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27246328 | |||||
| chr12:27246358
|
G | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(50): Show | 55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+2026G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246358 | ||||||
| chr12:27246440
|
A | G | 327 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(324): Show | 342 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.-12+2108A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246440 | ||||||
| chr12:27246548
|
T | G | 1 | a0001c0001t0015g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+2216T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246548 | ||||||
| chr12:27246692
|
C | A | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+2360C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246692 | ||||||
| chr12:27246750
|
G | GCACT | 251 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(248): Show | 264 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.-12+2419_-12+2422d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27246750 | |||||
| chr12:27246848
|
A | G | 251 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(248): Show | 264 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.-12+2516A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246848 | ||||||
| chr12:27246912
|
C | T | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+2580C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27246912 | ||||||
| chr12:27247167
|
C | T | 1 | a0001c0001t0008g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12+2835C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247167 | ||||||
| chr12:27247219
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(50): Show | 55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+2887A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247219 | ||||||
| chr12:27247313
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-12+2981G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247313 | ||||||
| chr12:27247531
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+3199G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247531 | ||||||
| chr12:27247656
|
C | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(324): Show | 342 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.-12+3324C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247656 | ||||||
| chr12:27247814
|
A | AT | 69 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(66): Show | 70 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12+3502dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | |||||
| chr12:27247814
|
A | ATTT | 9 | a0001c0001t0012g0352a0001c0002t0005g0004a0001c0002t0005g0350others(6): Show | 11 | HG00741.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+3500_-12+3502d others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | |||||
| chr12:27247814
|
AT | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(62): Show | 68 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.-12+3502delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27247814 | |||||
| chr12:27247879
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+3547A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247879 | ||||||
| chr12:27247918
|
G | A | 1 | a0001c0001t0008g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+3586G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247918 | ||||||
| chr12:27247973
|
C | T | 10 | a0001c0001t0001g0233a0001c0001t0002g0230a0001c0001t0002g0238others(7): Show | 10 | HG00639.hp2 HG01192.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+3641C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27247973 | ||||||
| chr12:27248039
|
T | G | 1 | a0001c0001t0004g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12+3707T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248039 | ||||||
| chr12:27248203
|
C | G | 1 | a0001c0001t0001g0330 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12+3871C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248203 | ||||||
| chr12:27248414
|
C | T | 150 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0001g0122others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-12+4082C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248414 | ||||||
| chr12:27248484
|
C | T | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+4152C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248484 | ||||||
| chr12:27248498
|
G | A | 1 | a0001c0003t0002g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12+4166G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248498 | ||||||
| chr12:27248534
|
C | A | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+4202C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248534 | ||||||
| chr12:27248637
|
GT | G | 27 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(24): Show | 30 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+4308delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27248637 | |||||
| chr12:27248678
|
A | G | 3 | a0001c0001t0005g0339a0001c0001t0006g0010a0001c0001t0008g0128 | 4 | HG02257.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+4346A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248678 | ||||||
| chr12:27248767
|
G | A | 18 | a0001c0001t0001g0101a0001c0001t0001g0129a0001c0001t0001g0130others(15): Show | 18 | HG00733.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4435G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248767 | ||||||
| chr12:27248948
|
A | C | 1 | a0001c0001t0006g0010 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-12+4616A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27248948 | ||||||
| chr12:27249254
|
A | G | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+4922A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249254 | ||||||
| chr12:27249330
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0005g0339a0001c0001t0006g0010a0001c0001t0008g0128 | 4 | HG02257.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+5014_-12+5021d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27249330 | |||||
| chr12:27249584
|
C | T | 22 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0320others(19): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+5252C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249584 | ||||||
| chr12:27249716
|
T | A | 1 | a0001c0001t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+5384T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249716 | ||||||
| chr12:27249776
|
G | A | 222 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(219): Show | 231 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.-12+5444G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249776 | ||||||
| chr12:27249826
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02486.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+5494G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249826 | ||||||
| chr12:27249829
|
C | T | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5497C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249829 | ||||||
| chr12:27249898
|
C | G | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+5566C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27249898 | ||||||
| chr12:27250254
|
C | T | 222 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(219): Show | 231 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.-12+5922C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250254 | ||||||
| chr12:27250281
|
C | T | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5949C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250281 | ||||||
| chr12:27250318
|
A | G | 7 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(4): Show | 7 | HG00438.hp1 HG00609.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+5986A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250318 | ||||||
| chr12:27250342
|
C | T | 2 | a0001c0001t0001g0313a0001c0002t0001g0312 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-12+6010C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250342 | ||||||
| chr12:27250529
|
T | G | 1 | a0001c0001t0003g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12+6197T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250529 | ||||||
| chr12:27250631
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+6299G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250631 | ||||||
| chr12:27250827
|
C | T | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+6495C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250827 | ||||||
| chr12:27250883
|
C | T | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+6551C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250883 | ||||||
| chr12:27250973
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-12+6641T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250973 | ||||||
| chr12:27250991
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-12+6659T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27250991 | ||||||
| chr12:27250996
|
C | CA | 24 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(21): Show | 27 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-12+6684dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | |||||
| chr12:27250996
|
CA | C | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 29 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+6684delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | |||||
| chr12:27250996
|
CAA | C | 217 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(214): Show | 226 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.-12+6683_-12+6684d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27250996 | |||||
| chr12:27251054
|
A | G | 27 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(24): Show | 30 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+6722A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251054 | ||||||
| chr12:27251068
|
C | T | 1 | a0001c0001t0005g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+6736C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251068 | ||||||
| chr12:27251114
|
T | A | 1 | a0001c0001t0006g0103 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-12+6782T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251114 | ||||||
| chr12:27251241
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-12+6909A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251241 | ||||||
| chr12:27251346
|
G | A | 326 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(323): Show | 340 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.-12+7014G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251346 | ||||||
| chr12:27251432
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-12+7100A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251432 | ||||||
| chr12:27251704
|
T | C | 1 | a0001c0001t0017g0276 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12+7372T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251704 | ||||||
| chr12:27251723
|
G | A | 15 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+7391G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251723 | ||||||
| chr12:27251835
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+7503G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251835 | ||||||
| chr12:27251870
|
C | T | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+7538C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251870 | ||||||
| chr12:27251929
|
G | A | 25 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(22): Show | 28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+7597G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251929 | ||||||
| chr12:27251977
|
T | C | 1 | a0001c0001t0006g0102 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12+7645T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27251977 | ||||||
| chr12:27251987
|
C | CT | 54 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(51): Show | 56 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12+7665dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27251987 | |||||
| chr12:27252010
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-12+7678C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252010 | ||||||
| chr12:27252072
|
C | T | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+7740C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252072 | ||||||
| chr12:27252201
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+7869A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252201 | ||||||
| chr12:27252215
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(50): Show | 55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+7883G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252215 | ||||||
| chr12:27252274
|
C | T | 1 | a0001c0001t0003g0335 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-12+7942C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252274 | ||||||
| chr12:27252420
|
A | AC | 153 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0001g0122others(150): Show | 156 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-12+8089dupC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27252420 | |||||
| chr12:27252504
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+8172T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252504 | ||||||
| chr12:27252677
|
C | T | 3 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | NA18961.hp2 NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-12+8345C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252677 | ||||||
| chr12:27252698
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+8366G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27252698 | ||||||
| chr12:27253069
|
T | C | 58 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(55): Show | 62 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-12+8737T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253069 | ||||||
| chr12:27253076
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(50): Show | 55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+8744T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253076 | ||||||
| chr12:27253129
|
G | C | 25 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(22): Show | 28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+8797G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253129 | ||||||
| chr12:27253214
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+8882T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253214 | ||||||
| chr12:27253304
|
G | A | 5 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(2): Show | 5 | HG02257.hp2 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+8972G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253304 | ||||||
| chr12:27253392
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-12+9060G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253392 | ||||||
| chr12:27253444
|
C | CTCCTT | 353 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(350): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-12+9114_-12+9115i others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27253444 | |||||
| chr12:27253733
|
T | C | 71 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060others(68): Show | 77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-12+9401T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253733 | ||||||
| chr12:27253785
|
A | G | 2 | a0001c0001t0011g0043a0001c0001t0011g0049 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12+9453A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253785 | ||||||
| chr12:27253786
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0277others(50): Show | 55 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12+9454C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253786 | ||||||
| chr12:27253801
|
G | T | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+9469G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253801 | ||||||
| chr12:27253814
|
G | A | 78 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(75): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-12+9482G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253814 | ||||||
| chr12:27253826
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0004g0256 | 2 | HG00099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-12+9494G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253826 | ||||||
| chr12:27253834
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | NA18971.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-12+9502G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253834 | ||||||
| chr12:27253943
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+9611C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27253943 | ||||||
| chr12:27254022
|
T | C | 25 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(22): Show | 28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+9690T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254022 | ||||||
| chr12:27254084
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0014g0108 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+9752A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254084 | ||||||
| chr12:27254093
|
T | G | 25 | a0001c0001t0001g0327a0001c0001t0001g0340a0001c0001t0004g0013others(22): Show | 28 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+9761T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254093 | ||||||
| chr12:27254330
|
A | G | 1 | a0001c0001t0005g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+9998A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254330 | ||||||
| chr12:27254389
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+10057A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254389 | ||||||
| chr12:27254401
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+10069G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254401 | ||||||
| chr12:27254435
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-12+10103C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254435 | ||||||
| chr12:27254436
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-12+10104C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254436 | ||||||
| chr12:27254642
|
A | T | 31 | a0001c0001t0001g0126a0001c0001t0001g0340a0001c0001t0002g0227others(28): Show | 34 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12+10310A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254642 | ||||||
| chr12:27254722
|
C | T | 195 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0001g0122others(192): Show | 202 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.-12+10390C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254722 | ||||||
| chr12:27254740
|
G | GA | 13 | a0001c0001t0001g0121a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG02015.hp1 HG02074.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+10411dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27254740 | |||||
| chr12:27254788
|
G | T | 324 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(321): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-12+10456G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254788 | ||||||
| chr12:27254796
|
C | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(353): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.-12+10464C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254796 | ||||||
| chr12:27254806
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-12+10474G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254806 | ||||||
| chr12:27254924
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-12+10592C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254924 | ||||||
| chr12:27254977
|
A | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(1): Show | 5 | HG02145.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+10645A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27254977 | ||||||
| chr12:27255054
|
A | C | 57 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0226others(54): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-12+10722A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255054 | ||||||
| chr12:27255091
|
T | C | 4 | a0001c0001t0001g0330a0001c0001t0002g0009a0001c0001t0002g0099others(1): Show | 5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+10759T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255091 | ||||||
| chr12:27255228
|
G | A | 1 | a0001c0001t0004g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12+10896G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255228 | ||||||
| chr12:27255263
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-12+10931T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255263 | ||||||
| chr12:27255454
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12+11122A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255454 | ||||||
| chr12:27255823
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-12+11491C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255823 | ||||||
| chr12:27255824
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0006g0232 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+11492G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255824 | ||||||
| chr12:27255845
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-12+11513T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255845 | ||||||
| chr12:27255978
|
G | A | 6 | a0001c0001t0001g0257a0001c0001t0001g0330a0001c0001t0006g0040others(3): Show | 6 | HG02723.hp2 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+11646G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255978 | ||||||
| chr12:27255980
|
G | A | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+11648G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27255980 | ||||||
| chr12:27256077
|
C | G | 1 | a0001c0001t0003g0186 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-12+11745C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256077 | ||||||
| chr12:27256143
|
G | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(249): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-12+11811G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256143 | ||||||
| chr12:27256153
|
T | C | 1 | a0001c0001t0002g0239 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+11821T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256153 | ||||||
| chr12:27256171
|
A | G | 1 | a0001c0001t0004g0272 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12+11839A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256171 | ||||||
| chr12:27256280
|
A | G | 1 | a0001c0001t0005g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+11948A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256280 | ||||||
| chr12:27256367
|
C | G | 1 | a0001c0001t0004g0002 | 3 | HG03669.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+12035C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256367 | ||||||
| chr12:27256569
|
G | A | 25 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(22): Show | 28 | HG00741.hp1 HG01123.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+12237G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256569 | ||||||
| chr12:27256951
|
G | C | 10 | a0001c0002t0005g0004a0001c0002t0005g0337a0001c0002t0005g0338others(7): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+12619G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27256951 | ||||||
| chr12:27257083
|
A | G | 2 | a0001c0001t0001g0327a0001c0001t0012g0352 | 2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-12+12751A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257083 | ||||||
| chr12:27257175
|
G | T | 2 | a0001c0001t0002g0107a0001c0001t0014g0108 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+12843G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257175 | ||||||
| chr12:27257231
|
G | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(250): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-12+12899G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257231 | ||||||
| chr12:27257236
|
C | A | 1 | a0001c0001t0004g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-12+12904C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257236 | ||||||
| chr12:27257247
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-12+12915T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257247 | ||||||
| chr12:27257286
|
G | C | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+12954G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257286 | ||||||
| chr12:27257489
|
T | C | 61 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(58): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+13157T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257489 | ||||||
| chr12:27257540
|
C | T | 3 | a0001c0001t0005g0339a0001c0001t0006g0005a0001c0001t0006g0010 | 5 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13208C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257540 | ||||||
| chr12:27257600
|
C | G | 70 | a0001c0001t0001g0330a0001c0001t0002g0055a0001c0001t0002g0056others(67): Show | 75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+13268C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257600 | ||||||
| chr12:27257691
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12+13359G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257691 | ||||||
| chr12:27257809
|
A | G | 70 | a0001c0001t0001g0330a0001c0001t0002g0055a0001c0001t0002g0056others(67): Show | 75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+13477A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257809 | ||||||
| chr12:27257833
|
G | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(108): Show | 113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-12+13501G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27257833 | ||||||
| chr12:27257864
|
C | CT | 63 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0173others(60): Show | 67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+13548dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27257864 | |||||
| chr12:27257864
|
CT | C | 46 | a0001c0001t0001g0326a0001c0001t0002g0111a0001c0001t0002g0112others(43): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-12+13548delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27257864 | |||||
| chr12:27258113
|
TC | T | 3 | a0001c0001t0005g0339a0001c0001t0006g0005a0001c0001t0006g0010 | 5 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13784delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258113 | |||||
| chr12:27258135
|
G | T | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+13803G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258135 | ||||||
| chr12:27258307
|
G | A | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+13975G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258307 | ||||||
| chr12:27258482
|
C | A | 1 | a0001c0001t0002g0179 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-12+14150C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258482 | ||||||
| chr12:27258510
|
G | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+14178G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258510 | ||||||
| chr12:27258609
|
G | GT | 9 | a0001c0001t0001g0330a0001c0001t0005g0011a0001c0001t0005g0125others(6): Show | 10 | HG02145.hp2 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+14278dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258609 | |||||
| chr12:27258667
|
G | A | 12 | a0001c0001t0001g0233a0001c0001t0002g0039a0001c0001t0002g0227others(9): Show | 12 | HG00639.hp2 HG01192.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+14335G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258667 | ||||||
| chr12:27258710
|
A | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(261): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-12+14378A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258710 | ||||||
| chr12:27258767
|
T | A | 60 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(57): Show | 64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+14435T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258767 | ||||||
| chr12:27258804
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-12+14472G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258804 | ||||||
| chr12:27258960
|
C | A | 1 | a0001c0001t0001g0330 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12+14628C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27258960 | ||||||
| chr12:27258969
|
C | CTT | 259 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(256): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-12+14638_-12+1463 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27258969 | |||||
| chr12:27259158
|
G | T | 1 | a0001c0001t0005g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-12+14826G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259158 | ||||||
| chr12:27259284
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0281 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+14952G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259284 | ||||||
| chr12:27259322
|
G | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(245): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-12+14990G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259322 | ||||||
| chr12:27259369
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12+15037C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259369 | ||||||
| chr12:27259401
|
T | C | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(56): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+15069T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259401 | ||||||
| chr12:27259436
|
C | T | 1 | a0001c0001t0006g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+15104C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259436 | ||||||
| chr12:27259471
|
A | G | 1 | a0001c0001t0015g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+15139A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259471 | ||||||
| chr12:27259531
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-12+15199G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259531 | ||||||
| chr12:27259580
|
G | T | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+15248G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259580 | ||||||
| chr12:27259641
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-12+15309C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259641 | ||||||
| chr12:27259693
|
G | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(197): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-12+15361G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259693 | ||||||
| chr12:27259754
|
A | G | 7 | a0001c0001t0001g0313a0001c0001t0001g0330a0001c0001t0005g0329others(4): Show | 7 | HG02809.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+15422A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259754 | ||||||
| chr12:27259959
|
T | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(162): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-12+15627T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259959 | ||||||
| chr12:27259966
|
T | C | 19 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0018others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12+15634T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27259966 | ||||||
| chr12:27260108
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-12+15776A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260108 | ||||||
| chr12:27260190
|
A | G | 1 | a0001c0001t0002g0223 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-12+15858A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260190 | ||||||
| chr12:27260293
|
A | G | 2 | a0001c0001t0004g0333a0001c0001t0004g0334 | 2 | NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-12+15961A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260293 | ||||||
| chr12:27260390
|
G | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(159): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.-12+16058G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260390 | ||||||
| chr12:27260483
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+16151C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260483 | ||||||
| chr12:27260554
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(56): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+16222C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260554 | ||||||
| chr12:27260563
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-12+16231G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260563 | ||||||
| chr12:27260832
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0125 | 3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-12+16500G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27260832 | ||||||
| chr12:27261117
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(4): Show | 9 | NA18942.hp2 NA18953.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+16785G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261117 | ||||||
| chr12:27261151
|
A | G | 14 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(11): Show | 17 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+16819A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261151 | ||||||
| chr12:27261166
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+16834T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261166 | ||||||
| chr12:27261216
|
T | G | 350 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(347): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-12+16884T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261216 | ||||||
| chr12:27261252
|
A | G | 10 | a0001c0001t0001g0233a0001c0001t0005g0339a0001c0001t0006g0005others(7): Show | 12 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+16920A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261252 | ||||||
| chr12:27261272
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+16940T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261272 | ||||||
| chr12:27261612
|
G | C | 258 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(255): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-12+17280G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261612 | ||||||
| chr12:27261779
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(254): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12+17447A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261779 | ||||||
| chr12:27261939
|
T | A | 10 | a0001c0002t0005g0004a0001c0002t0005g0337a0001c0002t0005g0338others(7): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+17607T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261939 | ||||||
| chr12:27261944
|
T | C | 61 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(58): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+17612T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27261944 | ||||||
| chr12:27262172
|
A | AAATCTC | 35 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(32): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+17842_-12+1784 others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262172 | |||||
| chr12:27262277
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+17945A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262277 | ||||||
| chr12:27262400
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(257): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-12+18068C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262400 | ||||||
| chr12:27262429
|
A | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-12+18097A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262429 | ||||||
| chr12:27262470
|
A | G | 1 | a0001c0001t0015g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+18138A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262470 | ||||||
| chr12:27262641
|
G | C | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+18309G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262641 | ||||||
| chr12:27262673
|
C | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0281 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+18341C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262673 | ||||||
| chr12:27262698
|
C | CT | 61 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(58): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+18367dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262698 | |||||
| chr12:27262704
|
C | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0002g0104others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+18372C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262704 | ||||||
| chr12:27262709
|
T | TA | 58 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(55): Show | 62 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+18393dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262709 | |||||
| chr12:27262709
|
TA | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(201): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-12+18393delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262709 | |||||
| chr12:27262800
|
A | AT | 125 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-12+18484dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | |||||
| chr12:27262800
|
A | ATT | 35 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0274others(32): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+18483_-12+1848 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | |||||
| chr12:27262800
|
AT | A | 60 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(57): Show | 64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+18484delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27262800 | |||||
| chr12:27262851
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+18519C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262851 | ||||||
| chr12:27262869
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-12+18537G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27262869 | ||||||
| chr12:27263022
|
C | T | 3 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0229 | 3 | HG00423.hp2 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-12+18690C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263022 | ||||||
| chr12:27263168
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12+18836T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263168 | ||||||
| chr12:27263349
|
G | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-12+19017G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263349 | ||||||
| chr12:27263365
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(174): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-12+19033C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263365 | ||||||
| chr12:27263404
|
C | CATGA | 61 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(58): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+19073_-12+1907 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27263404 | |||||
| chr12:27263404
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-12+19072C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263404 | ||||||
| chr12:27263482
|
G | T | 35 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(32): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+19150G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263482 | ||||||
| chr12:27263502
|
G | A | 6 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0002g0104others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+19170G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263502 | ||||||
| chr12:27263560
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-12+19228C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263560 | ||||||
| chr12:27263648
|
A | G | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+19316A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263648 | ||||||
| chr12:27263835
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0006g0232 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+19503C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263835 | ||||||
| chr12:27263899
|
T | G | 1 | a0001c0001t0002g0173 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-12+19567T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263899 | ||||||
| chr12:27263948
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+19616C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263948 | ||||||
| chr12:27263977
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-12+19645G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27263977 | ||||||
| chr12:27264289
|
C | T | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+19957C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264289 | ||||||
| chr12:27264357
|
A | G | 62 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(59): Show | 66 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+20025A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264357 | ||||||
| chr12:27264442
|
C | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-12+20110C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264442 | ||||||
| chr12:27264594
|
A | G | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+20262A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264594 | ||||||
| chr12:27264765
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+20433G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27264765 | ||||||
| chr12:27265178
|
T | A | 1 | a0001c0001t0004g0333 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-12+20846T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265178 | ||||||
| chr12:27265266
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+20934G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265266 | ||||||
| chr12:27265277
|
T | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(118): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+20945T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265277 | ||||||
| chr12:27265315
|
T | G | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+20983T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265315 | ||||||
| chr12:27265323
|
C | T | 1 | a0001c0001t0006g0010 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-12+20991C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265323 | ||||||
| chr12:27265434
|
T | C | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(56): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+21102T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265434 | ||||||
| chr12:27265579
|
T | C | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+21247T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265579 | ||||||
| chr12:27265601
|
A | T | 1 | a0001c0001t0002g0222 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-12+21269A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265601 | ||||||
| chr12:27265629
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-12+21297A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265629 | ||||||
| chr12:27265736
|
G | A | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+21404G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265736 | ||||||
| chr12:27265800
|
T | C | 2 | a0001c0001t0002g0009a0001c0001t0002g0099 | 3 | HG02717.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-12+21468T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265800 | ||||||
| chr12:27265897
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | NA18947.hp1 NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-12+21565A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27265897 | ||||||
| chr12:27266129
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+21797T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266129 | ||||||
| chr12:27266190
|
A | T | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+21858A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266190 | ||||||
| chr12:27266479
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+22147C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266479 | ||||||
| chr12:27266545
|
T | G | 1 | a0001c0001t0001g0325 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-12+22213T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266545 | ||||||
| chr12:27266900
|
C | G | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+22568C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27266900 | ||||||
| chr12:27267106
|
T | A | 2 | a0001c0001t0004g0259a0001c0001t0004g0260 | 2 | HG01070.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-12+22774T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267106 | ||||||
| chr12:27267318
|
A | G | 9 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0010others(6): Show | 11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+22986A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267318 | ||||||
| chr12:27267354
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+23022G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267354 | ||||||
| chr12:27267388
|
T | A | 1 | a0001c0002t0001g0312 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-12+23056T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267388 | ||||||
| chr12:27267414
|
C | T | 1 | a0001c0001t0004g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-12+23082C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267414 | ||||||
| chr12:27267488
|
G | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(260): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12+23156G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267488 | ||||||
| chr12:27267577
|
T | A | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192others(7): Show | 10 | HG00544.hp1 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+23245T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267577 | ||||||
| chr12:27267592
|
A | G | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+23260A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267592 | ||||||
| chr12:27267639
|
G | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+23307G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267639 | ||||||
| chr12:27267731
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-12+23399T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267731 | ||||||
| chr12:27267737
|
T | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(261): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-12+23405T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267737 | ||||||
| chr12:27267738
|
TC | T | 264 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(261): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-12+23407delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267738 | ||||||
| chr12:27267773
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(253): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-12+23441T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267773 | ||||||
| chr12:27267780
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-12+23448A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27267780 | ||||||
| chr12:27268089
|
C | T | 6 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0002g0104others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+23757C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268089 | ||||||
| chr12:27268170
|
TGTTA | T | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+23843_-12+2384 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27268170 | |||||
| chr12:27268193
|
T | TATACATA others(8): Show |
4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+23861_-12+2386 others(19): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268193 | ||||||
| chr12:27268218
|
T | G | 35 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(32): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+23886T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268218 | ||||||
| chr12:27268223
|
C | T | 20 | a0001c0001t0004g0002a0001c0001t0004g0247a0001c0001t0004g0255others(17): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+23891C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268223 | ||||||
| chr12:27268362
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-12+24030T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268362 | ||||||
| chr12:27268487
|
A | G | 2 | a0001c0001t0001g0313a0001c0002t0001g0312 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-12+24155A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268487 | ||||||
| chr12:27268541
|
C | G | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+24209C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268541 | ||||||
| chr12:27268566
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-12+24234C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268566 | ||||||
| chr12:27268571
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+24239A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268571 | ||||||
| chr12:27268804
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0010others(1): Show | 6 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+24472C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268804 | ||||||
| chr12:27268857
|
C | G | 2 | a0001c0001t0001g0233a0001c0001t0006g0232 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+24525C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268857 | ||||||
| chr12:27268891
|
G | A | 9 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0010others(6): Show | 11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+24559G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268891 | ||||||
| chr12:27268904
|
T | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(267): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-12+24572T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268904 | ||||||
| chr12:27268910
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+24578A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268910 | ||||||
| chr12:27268914
|
C | A | 2 | a0001c0001t0006g0005a0001c0001t0006g0050 | 3 | HG02055.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-12+24582C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268914 | ||||||
| chr12:27268962
|
G | T | 2 | a0001c0001t0005g0011a0001c0001t0005g0125 | 3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-12+24630G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27268962 | ||||||
| chr12:27269180
|
A | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+24848A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269180 | ||||||
| chr12:27269232
|
C | A | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-12+24900C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269232 | ||||||
| chr12:27269262
|
T | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(228): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-12+24930T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269262 | ||||||
| chr12:27269314
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-12+24982G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269314 | ||||||
| chr12:27269334
|
T | C | 2 | a0001c0001t0004g0261a0001c0001t0004g0270 | 2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-12+25002T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269334 | ||||||
| chr12:27269625
|
G | A | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+25293G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269625 | ||||||
| chr12:27269708
|
T | A | 61 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0003g0006others(58): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+25376T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269708 | ||||||
| chr12:27269808
|
G | A | 266 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(263): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-12+25476G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269808 | ||||||
| chr12:27269840
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0006g0232 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12+25508G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269840 | ||||||
| chr12:27269844
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12+25512T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269844 | ||||||
| chr12:27269850
|
C | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+25518C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269850 | ||||||
| chr12:27269898
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | NA18960.hp2 NA19010.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-12+25566C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269898 | ||||||
| chr12:27269912
|
A | C | 1 | a0001c0001t0004g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12+25580A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269912 | ||||||
| chr12:27269925
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-12+25593G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269925 | ||||||
| chr12:27269953
|
C | T | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+25621C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27269953 | ||||||
| chr12:27270010
|
C | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+25678C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270010 | ||||||
| chr12:27270085
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+25753C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270085 | ||||||
| chr12:27270268
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12+25936T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270268 | ||||||
| chr12:27270365
|
C | T | 1 | a0001c0001t0006g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-12+26033C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270365 | ||||||
| chr12:27270678
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+26346C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270678 | ||||||
| chr12:27270682
|
T | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-12+26350T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270682 | ||||||
| chr12:27270737
|
C | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-12+26405C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270737 | ||||||
| chr12:27270786
|
T | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+26454T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270786 | ||||||
| chr12:27270809
|
T | C | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+26477T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27270809 | ||||||
| chr12:27271001
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-12+26669A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271001 | ||||||
| chr12:27271097
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-26613A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271097 | ||||||
| chr12:27271131
|
C | T | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-26579C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271131 | ||||||
| chr12:27271338
|
C | T | 267 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-11-26372C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271338 | ||||||
| chr12:27271464
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-11-26246G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271464 | ||||||
| chr12:27271535
|
G | C | 8 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0010others(5): Show | 10 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-26175G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271535 | ||||||
| chr12:27271598
|
T | A | 35 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(32): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-11-26112T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271598 | ||||||
| chr12:27271645
|
A | T | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-11-26065A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271645 | ||||||
| chr12:27271658
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-11-26052A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271658 | ||||||
| chr12:27271726
|
G | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(169): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-11-25984G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271726 | ||||||
| chr12:27271844
|
C | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-25866C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271844 | ||||||
| chr12:27271854
|
C | T | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-25856C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27271854 | ||||||
| chr12:27272135
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-25575T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272135 | ||||||
| chr12:27272433
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(154): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-11-25277T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272433 | ||||||
| chr12:27272457
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-11-25253A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272457 | ||||||
| chr12:27272479
|
TC | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0099 | 3 | HG02717.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11-25228delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27272479 | |||||
| chr12:27272555
|
A | G | 4 | a0001c0001t0001g0288a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-25155A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272555 | ||||||
| chr12:27272943
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-11-24767G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272943 | ||||||
| chr12:27272986
|
A | C | 60 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(57): Show | 64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-11-24724A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27272986 | ||||||
| chr12:27273273
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-11-24437C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273273 | ||||||
| chr12:27273470
|
G | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0044a0001c0001t0003g0047others(2): Show | 6 | NA18948.hp1 NA18975.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-24240G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273470 | ||||||
| chr12:27273546
|
A | G | 239 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(236): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11-24164A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273546 | ||||||
| chr12:27273705
|
AAATCTGG others(1): Show |
A | 20 | a0001c0001t0001g0274a0001c0001t0004g0002a0001c0001t0004g0255others(17): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-24002_-11-2399 others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27273705 | |||||
| chr12:27273865
|
A | G | 15 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(12): Show | 16 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-23845A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273865 | ||||||
| chr12:27273905
|
G | T | 21 | a0001c0001t0001g0274a0001c0001t0004g0002a0001c0001t0004g0247others(18): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.-11-23805G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273905 | ||||||
| chr12:27273977
|
G | T | 7 | a0001c0001t0006g0050a0001c0001t0006g0102a0001c0001t0006g0103others(4): Show | 7 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-23733G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27273977 | ||||||
| chr12:27274129
|
G | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(266): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-11-23581G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274129 | ||||||
| chr12:27274192
|
G | T | 1 | a0001c0001t0002g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-11-23518G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274192 | ||||||
| chr12:27274233
|
C | CA | 22 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(19): Show | 25 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11-23462dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | |||||
| chr12:27274233
|
C | CAA | 147 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11-23463_-11-2346 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | |||||
| chr12:27274233
|
C | CAAA | 90 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(87): Show | 95 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-11-23464_-11-2346 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27274233 | |||||
| chr12:27274472
|
C | A | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-23238C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274472 | ||||||
| chr12:27274722
|
G | A | 15 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(12): Show | 16 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-22988G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274722 | ||||||
| chr12:27274773
|
A | G | 1 | a0001c0001t0004g0013 | 2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-11-22937A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274773 | ||||||
| chr12:27274880
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-22830C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274880 | ||||||
| chr12:27274929
|
T | C | 1 | a0001c0001t0004g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-11-22781T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274929 | ||||||
| chr12:27274984
|
A | G | 83 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0179others(80): Show | 87 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11-22726A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27274984 | ||||||
| chr12:27275023
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(113): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-11-22687A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275023 | ||||||
| chr12:27275037
|
A | T | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-22673A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275037 | ||||||
| chr12:27275267
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11-22443A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275267 | ||||||
| chr12:27275342
|
C | CT | 171 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(168): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11-22350dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27275342 | |||||
| chr12:27275637
|
A | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(258): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-11-22073A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275637 | ||||||
| chr12:27275799
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-21911A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275799 | ||||||
| chr12:27275987
|
C | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-21723C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27275987 | ||||||
| chr12:27276021
|
T | C | 36 | a0001c0001t0001g0274a0001c0001t0002g0111a0001c0001t0002g0112others(33): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11-21689T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276021 | ||||||
| chr12:27276034
|
A | G | 36 | a0001c0001t0001g0274a0001c0001t0002g0111a0001c0001t0002g0112others(33): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11-21676A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276034 | ||||||
| chr12:27276112
|
T | G | 1 | a0001c0001t0003g0063 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-11-21598T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276112 | ||||||
| chr12:27276318
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-11-21392T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276318 | ||||||
| chr12:27276597
|
G | A | 22 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0003g0015others(19): Show | 22 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-21113G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276597 | ||||||
| chr12:27276939
|
C | T | 1 | a0001c0001t0004g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-11-20771C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27276939 | ||||||
| chr12:27277060
|
T | A | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-20650T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277060 | ||||||
| chr12:27277233
|
ATTAC | A | 24 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(21): Show | 24 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-20475_-11-2047 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277233 | |||||
| chr12:27277240
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0281 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-20470G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277240 | ||||||
| chr12:27277242
|
A | G | 57 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0001g0274others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-11-20468A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277242 | ||||||
| chr12:27277326
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-20384G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277326 | ||||||
| chr12:27277354
|
A | AAC | 232 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(229): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-11-20342_-11-2034 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277354 | |||||
| chr12:27277392
|
C | CCA | 6 | a0001c0001t0005g0328a0001c0001t0005g0329a0001c0003t0002g0117others(3): Show | 6 | HG00735.hp1 HG01433.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-20289_-11-2028 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | |||||
| chr12:27277392
|
CCA | C | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(124): Show | 133 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11-20289_-11-2028 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | |||||
| chr12:27277392
|
CCACA | C | 13 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0121others(10): Show | 13 | HG01346.hp2 HG01358.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-20291_-11-2028 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | |||||
| chr12:27277392
|
CCACACA | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-11-20293_-11-2028 others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | |||||
| chr12:27277392
|
CCACACAC others(3): Show |
C | 2 | a0001c0001t0001g0233a0001c0001t0006g0232 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-11-20297_-11-2028 others(14): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27277392 | |||||
| chr12:27277400
|
A | C | 1 | a0001c0001t0004g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-20310A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277400 | ||||||
| chr12:27277563
|
A | T | 1 | a0001c0001t0015g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-20147A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277563 | ||||||
| chr12:27277623
|
T | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-20087T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277623 | ||||||
| chr12:27277791
|
T | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-19919T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277791 | ||||||
| chr12:27277938
|
G | A | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11-19772G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27277938 | ||||||
| chr12:27278004
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0232 | 4 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-19706C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278004 | ||||||
| chr12:27278413
|
A | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-11-19297A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278413 | ||||||
| chr12:27278532
|
A | G | 27 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0002g0104others(24): Show | 30 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.-11-19178A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278532 | ||||||
| chr12:27278645
|
G | A | 27 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0002g0104others(24): Show | 30 | HG00741.hp1 HG01361.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.-11-19065G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278645 | ||||||
| chr12:27278929
|
A | C | 1 | a0001c0001t0001g0306 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11-18781A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278929 | ||||||
| chr12:27278989
|
T | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(261): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-11-18721T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27278989 | ||||||
| chr12:27279067
|
G | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-18643G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279067 | ||||||
| chr12:27279104
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11-18606C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279104 | ||||||
| chr12:27279452
|
T | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(258): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-11-18258T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279452 | ||||||
| chr12:27279485
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-11-18225G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279485 | ||||||
| chr12:27279506
|
C | T | 1 | a0001c0001t0004g0343 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-11-18204C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279506 | ||||||
| chr12:27279688
|
A | AT | 175 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(172): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-11-18005dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27279688 | |||||
| chr12:27279688
|
A | ATT | 59 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0279others(56): Show | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-18006_-11-1800 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27279688 | |||||
| chr12:27279688
|
A | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0340a0001c0001t0003g0081others(1): Show | 4 | HG00738.hp1 HG00738.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-18022A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279688 | ||||||
| chr12:27279709
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 8 | NA18942.hp2 NA18953.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-18001A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27279709 | ||||||
| chr12:27280098
|
G | A | 10 | a0001c0002t0005g0004a0001c0002t0005g0337a0001c0002t0005g0338others(7): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-17612G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280098 | ||||||
| chr12:27280281
|
A | G | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192others(7): Show | 10 | HG00544.hp1 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-17429A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280281 | ||||||
| chr12:27280334
|
G | T | 1 | a0001c0001t0004g0175 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-11-17376G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280334 | ||||||
| chr12:27280819
|
T | G | 9 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0010others(6): Show | 11 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-16891T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280819 | ||||||
| chr12:27280955
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-16755T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280955 | ||||||
| chr12:27280997
|
G | A | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-16713G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27280997 | ||||||
| chr12:27281054
|
TGGCTTTA others(324): Show |
T | 267 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-11-16639_-11-1630 others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281054 | |||||
| chr12:27281067
|
G | GT | 25 | a0001c0001t0002g0055a0001c0001t0002g0062a0001c0001t0002g0110others(22): Show | 25 | HG00544.hp1 HG00735.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11-16607dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281067
|
G | GTT | 20 | a0001c0001t0002g0001a0001c0001t0002g0056a0001c0001t0002g0078others(17): Show | 22 | HG01192.hp1 HG02071.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-16608_-11-1660 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281067
|
G | GTTT | 13 | a0001c0001t0002g0109a0001c0001t0002g0173a0001c0001t0002g0179others(10): Show | 13 | HG00597.hp2 HG02559.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-16609_-11-1660 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281067
|
G | GTTTT | 6 | a0001c0001t0002g0174a0001c0001t0002g0202a0001c0001t0002g0203others(3): Show | 6 | HG02809.hp2 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-16610_-11-1660 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281067
|
G | GTTTTT | 8 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0204others(5): Show | 8 | HG00438.hp2 HG01943.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11-16611_-11-1660 others(9): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281067
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11-16617_-11-1660 others(15): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27281067 | |||||
| chr12:27281074
|
T | G | 1 | a0001c0001t0002g0206 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-11-16636T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281074 | ||||||
| chr12:27281155
|
G | T | 1 | a0001c0001t0002g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-16555G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281155 | ||||||
| chr12:27281736
|
G | T | 6 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(3): Show | 6 | HG01361.hp2 HG03209.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-15974G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281736 | ||||||
| chr12:27281834
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11-15876A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281834 | ||||||
| chr12:27281865
|
T | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(118): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-11-15845T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281865 | ||||||
| chr12:27281905
|
G | A | 258 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(255): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-11-15805G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281905 | ||||||
| chr12:27281918
|
C | G | 4 | a0001c0001t0006g0040a0001c0001t0008g0128a0001c0001t0008g0280others(1): Show | 4 | HG02809.hp1 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-15792C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281918 | ||||||
| chr12:27281937
|
G | C | 2 | a0001c0001t0011g0043a0001c0001t0011g0049 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-15773G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281937 | ||||||
| chr12:27281953
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-11-15757T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27281953 | ||||||
| chr12:27282008
|
C | A | 1 | a0001c0001t0004g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-15702C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282008 | ||||||
| chr12:27282065
|
A | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-11-15645A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282065 | ||||||
| chr12:27282358
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-11-15352G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282358 | ||||||
| chr12:27282424
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-11-15286A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282424 | ||||||
| chr12:27282459
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-15251A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282459 | ||||||
| chr12:27282468
|
A | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(255): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-11-15242A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282468 | ||||||
| chr12:27282530
|
G | GT | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(56): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-15170dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27282530 | |||||
| chr12:27282653
|
G | A | 59 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(56): Show | 63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-15057G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282653 | ||||||
| chr12:27282954
|
T | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-11-14756T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27282954 | ||||||
| chr12:27283112
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-11-14598A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283112 | ||||||
| chr12:27283227
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-11-14483T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283227 | ||||||
| chr12:27283265
|
T | C | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-14445T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283265 | ||||||
| chr12:27283273
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-11-14437T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283273 | ||||||
| chr12:27283394
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-14316T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283394 | ||||||
| chr12:27283422
|
A | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(235): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-11-14288A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283422 | ||||||
| chr12:27283446
|
T | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(256): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-11-14264T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283446 | ||||||
| chr12:27283542
|
C | A | 1 | a0001c0001t0002g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11-14168C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283542 | ||||||
| chr12:27283566
|
A | T | 1 | a0001c0001t0015g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-14144A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283566 | ||||||
| chr12:27283811
|
T | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-13899T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283811 | ||||||
| chr12:27283866
|
A | G | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-13844A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27283866 | ||||||
| chr12:27284203
|
C | T | 1 | a0001c0001t0006g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-11-13507C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284203 | ||||||
| chr12:27284235
|
G | GGGGTA | 4 | a0001c0001t0001g0233a0001c0001t0006g0005a0001c0001t0006g0050others(1): Show | 5 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-13473_-11-1346 others(9): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27284235 | |||||
| chr12:27284610
|
G | A | 1 | a0001c0001t0009g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-13100G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284610 | ||||||
| chr12:27284902
|
C | T | 3 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0229 | 3 | HG00423.hp2 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-11-12808C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27284902 | ||||||
| chr12:27285101
|
A | G | 16 | a0001c0001t0001g0307a0001c0001t0003g0027a0001c0001t0003g0028others(13): Show | 16 | HG00642.hp2 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-12609A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285101 | ||||||
| chr12:27285125
|
A | T | 1 | a0001c0001t0004g0255 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11-12585A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285125 | ||||||
| chr12:27285159
|
T | C | 1 | a0001c0001t0002g0214 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-11-12551T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285159 | ||||||
| chr12:27285387
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(10): Show | 15 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-12323A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285387 | ||||||
| chr12:27285501
|
T | A | 1 | a0001c0002t0005g0338 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11-12209T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285501 | ||||||
| chr12:27285541
|
C | G | 1 | a0001c0001t0003g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-11-12169C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285541 | ||||||
| chr12:27285606
|
AG | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0125 | 3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-11-12101delG | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27285606 | |||||
| chr12:27285623
|
C | G | 1 | a0001c0001t0002g0238 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-11-12087C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285623 | ||||||
| chr12:27285765
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-11-11945A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285765 | ||||||
| chr12:27285863
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11-11847T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285863 | ||||||
| chr12:27285946
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-11764A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27285946 | ||||||
| chr12:27286083
|
G | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-11627G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286083 | ||||||
| chr12:27286224
|
T | C | 5 | a0001c0001t0004g0341a0001c0001t0004g0345a0001c0001t0004g0346others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-11486T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286224 | ||||||
| chr12:27286242
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0002g0208 | 2 | NA18954.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-11-11468T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286242 | ||||||
| chr12:27286335
|
T | C | 30 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(27): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11-11375T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286335 | ||||||
| chr12:27286398
|
CTGTT | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11307_-11-1130 others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27286398 | |||||
| chr12:27286408
|
A | G | 12 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(9): Show | 14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11-11302A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286408 | ||||||
| chr12:27286424
|
C | G | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-11286C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286424 | ||||||
| chr12:27286723
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-10987C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286723 | ||||||
| chr12:27286747
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-11-10963G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286747 | ||||||
| chr12:27286833
|
C | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02486.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-11-10877C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286833 | ||||||
| chr12:27286910
|
G | A | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-10800G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27286910 | ||||||
| chr12:27287018
|
C | T | 42 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0053others(39): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-10692C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287018 | ||||||
| chr12:27287101
|
C | CT | 28 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(25): Show | 31 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11-10593dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27287101 | |||||
| chr12:27287163
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-10547G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287163 | ||||||
| chr12:27287191
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11-10519C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287191 | ||||||
| chr12:27287251
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-10459G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27287251 | ||||||
| chr12:27287758
|
A | AT | 2 | a0001c0001t0001g0165a0001c0001t0004g0002 | 4 | HG03669.hp1 HG04204.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9946dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27287758 | |||||
| chr12:27288008
|
G | A | 21 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(18): Show | 24 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-9702G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288008 | ||||||
| chr12:27288192
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11-9518C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288192 | ||||||
| chr12:27288290
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11-9420T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288290 | ||||||
| chr12:27288500
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-11-9210A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288500 | ||||||
| chr12:27288578
|
C | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-9132C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288578 | ||||||
| chr12:27288724
|
T | G | 1 | a0001c0001t0002g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-8986T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288724 | ||||||
| chr12:27288763
|
C | A | 30 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(27): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11-8947C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288763 | ||||||
| chr12:27288825
|
C | T | 4 | a0001c0001t0007g0176a0001c0001t0007g0231a0001c0001t0007g0236others(1): Show | 4 | HG02809.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-8885C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288825 | ||||||
| chr12:27288826
|
G | A | 1 | a0001c0001t0005g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11-8884G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288826 | ||||||
| chr12:27288899
|
A | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(260): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-11-8811A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288899 | ||||||
| chr12:27288968
|
C | A | 3 | a0001c0001t0003g0079a0001c0001t0003g0084a0001c0001t0003g0085 | 3 | HG00423.hp1 NA18612.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-11-8742C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27288968 | ||||||
| chr12:27289139
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(8): Show | 13 | NA18942.hp2 NA18951.hp1 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-8571A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289139 | ||||||
| chr12:27289229
|
G | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0055others(74): Show | 79 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-11-8481G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289229 | ||||||
| chr12:27289301
|
C | CTCTTAAT others(3): Show |
20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-8407_-11-8398d others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27289301 | |||||
| chr12:27289356
|
T | A | 2 | a0001c0001t0004g0261a0001c0001t0004g0270 | 2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-11-8354T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289356 | ||||||
| chr12:27289357
|
A | T | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11-8353A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27289357 | ||||||
| chr12:27290025
|
G | A | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-7685G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290025 | ||||||
| chr12:27290136
|
G | A | 12 | a0001c0001t0004g0013a0001c0001t0004g0336a0001c0001t0004g0341others(9): Show | 13 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-7574G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290136 | ||||||
| chr12:27290244
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-11-7466A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290244 | ||||||
| chr12:27290365
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-11-7345G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290365 | ||||||
| chr12:27290697
|
G | C | 1 | a0001c0001t0001g0326 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-11-7013G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290697 | ||||||
| chr12:27290826
|
T | G | 1 | a0001c0001t0004g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11-6884T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27290826 | ||||||
| chr12:27291017
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-11-6693A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291017 | ||||||
| chr12:27291019
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-6691C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291019 | ||||||
| chr12:27291226
|
A | G | 1 | a0001c0001t0004g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-6484A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291226 | ||||||
| chr12:27291313
|
C | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11-6397C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291313 | ||||||
| chr12:27291584
|
A | G | 1 | a0001c0001t0006g0010 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-11-6126A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291584 | ||||||
| chr12:27291640
|
A | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-6070A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291640 | ||||||
| chr12:27291641
|
G | T | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-6069G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291641 | ||||||
| chr12:27291745
|
T | G | 5 | a0001c0001t0002g0183a0001c0001t0002g0215a0001c0001t0002g0218others(2): Show | 5 | NA18975.hp2 NA18981.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-5965T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291745 | ||||||
| chr12:27291876
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0071 | 3 | NA18943.hp2 NA18988.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-11-5834C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291876 | ||||||
| chr12:27291991
|
G | A | 1 | a0001c0001t0004g0333 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-11-5719G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27291991 | ||||||
| chr12:27292151
|
T | C | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-11-5559T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292151 | ||||||
| chr12:27292338
|
TTCTTGTT others(11): Show |
T | 26 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(23): Show | 30 | HG00597.hp1 HG00673.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11-5331_-11-5314d others(20): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27292338 | |||||
| chr12:27292404
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-5306A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292404 | ||||||
| chr12:27292599
|
A | G | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11-5111A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292599 | ||||||
| chr12:27292605
|
T | G | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-5105T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292605 | ||||||
| chr12:27292615
|
C | CTACT | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11-5094_-11-5091d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27292615 | |||||
| chr12:27292901
|
T | C | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-4809T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292901 | ||||||
| chr12:27292954
|
T | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(99): Show | 107 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.-11-4756T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27292954 | ||||||
| chr12:27293262
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-11-4448A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293262 | ||||||
| chr12:27293346
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0014g0108 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11-4364G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293346 | ||||||
| chr12:27293597
|
GGGCCAGA others(23): Show |
G | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-4112_-11-4083d others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293597 | ||||||
| chr12:27293696
|
A | G | 1 | a0001c0001t0004g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-4014A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293696 | ||||||
| chr12:27293872
|
T | G | 314 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(311): Show | 328 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.-11-3838T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293872 | ||||||
| chr12:27293913
|
T | A | 1 | a0001c0001t0004g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-3797T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27293913 | ||||||
| chr12:27293996
|
CAG | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-3712_-11-3711d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27293996 | |||||
| chr12:27294118
|
A | G | 2 | a0001c0002t0005g0351a0001c0002t0005g0357 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-11-3592A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294118 | ||||||
| chr12:27294317
|
C | T | 23 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(20): Show | 26 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-11-3393C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294317 | ||||||
| chr12:27294349
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11-3361A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294349 | ||||||
| chr12:27294433
|
GGAGGTGG others(1160): Show |
G | 1 | a0001c0001t0002g0308 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-11-3275_-11-2109d others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294433 | |||||
| chr12:27294463
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-11-3247C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294463 | ||||||
| chr12:27294504
|
C | CA | 7 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-3188dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | |||||
| chr12:27294504
|
CA | C | 100 | a0001c0001t0001g0157a0001c0001t0001g0319a0001c0001t0002g0001others(97): Show | 104 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.-11-3188delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | |||||
| chr12:27294504
|
CAA | C | 19 | a0001c0001t0002g0177a0001c0001t0002g0213a0001c0001t0003g0015others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-3189_-11-3188d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294504 | |||||
| chr12:27294526
|
G | A | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0050others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-3184G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294526 | ||||||
| chr12:27294710
|
CT | C | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-2987delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294710 | |||||
| chr12:27294879
|
T | TA | 34 | a0001c0001t0001g0165a0001c0001t0001g0327a0001c0001t0003g0066others(31): Show | 36 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11-2815dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294879 | |||||
| chr12:27294879
|
TA | T | 7 | a0001c0001t0001g0324a0001c0001t0002g0201a0001c0001t0002g0202others(4): Show | 7 | HG00438.hp1 HG03209.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-2815delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 27294879 | |||||
| chr12:27294897
|
T | C | 1 | a0001c0001t0003g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-2813T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294897 | ||||||
| chr12:27294990
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-11-2720G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27294990 | ||||||
| chr12:27295542
|
G | A | 1 | a0001c0001t0004g0341 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-11-2168G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295542 | ||||||
| chr12:27295563
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-2147A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295563 | ||||||
| chr12:27295735
|
C | T | 1 | a0001c0001t0004g0266 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11-1975C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295735 | ||||||
| chr12:27295890
|
T | G | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-1820T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295890 | ||||||
| chr12:27295959
|
T | C | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-1751T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27295959 | ||||||
| chr12:27296276
|
A | G | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-1434A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296276 | ||||||
| chr12:27296523
|
A | G | 1 | a0001c0001t0012g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11-1187A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296523 | ||||||
| chr12:27296610
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-1100G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296610 | ||||||
| chr12:27296643
|
G | T | 1 | a0001c0001t0001g0294 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-11-1067G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296643 | ||||||
| chr12:27296793
|
C | T | 1 | a0001c0001t0006g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-11-917C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296793 | ||||||
| chr12:27296881
|
G | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(262): Show | 275 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.-11-829G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27296881 | ||||||
| chr12:27297091
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-619T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297091 | ||||||
| chr12:27297400
|
T | G | 1 | a0001c0001t0002g0200 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-11-310T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297400 | ||||||
| chr12:27297663
|
G | C | 11 | a0001c0001t0004g0013a0001c0001t0004g0341a0001c0001t0004g0342others(8): Show | 12 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-47G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297663 | ||||||
| chr12:27297666
|
G | T | 1 | a0001c0001t0003g0093 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11-44G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 1/13 | chr12 | 27297666 | ||||||
| chr12:27298001
|
A | T | 11 | a0001c0002t0001g0312a0001c0002t0005g0004a0001c0002t0005g0337others(8): Show | 13 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.134+147A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298001 | ||||||
| chr12:27298066
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.134+212G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298066 | ||||||
| chr12:27298073
|
A | G | 106 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(103): Show | 111 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.134+219A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298073 | ||||||
| chr12:27298252
|
A | G | 1 | a0001c0001t0004g0265 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.134+398A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298252 | ||||||
| chr12:27298288
|
A | C | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(124): Show | 135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.134+434A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298288 | ||||||
| chr12:27298296
|
G | A | 1 | a0001c0001t0005g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.134+442G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298296 | ||||||
| chr12:27298358
|
GAAGGCAG others(9): Show |
G | 1 | a0001c0001t0001g0317 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.134+510_134+525del others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 27298358 | |||||
| chr12:27298513
|
A | G | 13 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(10): Show | 15 | HG00642.hp2 HG00673.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.134+659A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298513 | ||||||
| chr12:27298667
|
A | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+813A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298667 | ||||||
| chr12:27298685
|
CAG | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+832_134+833del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298685 | ||||||
| chr12:27298703
|
G | T | 8 | a0001c0001t0003g0006a0001c0001t0003g0045a0001c0001t0003g0046others(5): Show | 9 | HG00408.hp2 HG00423.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.134+849G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298703 | ||||||
| chr12:27298769
|
G | C | 1 | a0001c0001t0003g0089 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.134+915G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298769 | ||||||
| chr12:27298807
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.134+953G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298807 | ||||||
| chr12:27298872
|
C | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(90): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.134+1018C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27298872 | ||||||
| chr12:27299096
|
G | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+1242G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299096 | ||||||
| chr12:27299159
|
A | C | 1 | a0001c0001t0002g0110 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134+1305A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299159 | ||||||
| chr12:27299430
|
A | C | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+1576A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299430 | ||||||
| chr12:27299512
|
A | G | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134+1658A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299512 | ||||||
| chr12:27299576
|
C | T | 93 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(90): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.134+1722C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299576 | ||||||
| chr12:27299609
|
C | T | 2 | a0001c0001t0006g0005a0001c0001t0006g0232 | 3 | HG00639.hp2 HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.134+1755C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27299609 | ||||||
| chr12:27300079
|
A | G | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135-2058A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300079 | ||||||
| chr12:27300318
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.135-1819G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300318 | ||||||
| chr12:27300446
|
A | G | 1 | a0001c0001t0006g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.135-1691A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300446 | ||||||
| chr12:27300478
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(10): Show | 15 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135-1659A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300478 | ||||||
| chr12:27300488
|
A | G | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135-1649A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300488 | ||||||
| chr12:27300720
|
G | C | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.135-1417G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300720 | ||||||
| chr12:27300852
|
T | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135-1285T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27300852 | ||||||
| chr12:27301344
|
C | T | 1 | a0001c0001t0010g0332 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.135-793C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301344 | ||||||
| chr12:27301345
|
G | A | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0050others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.135-792G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301345 | ||||||
| chr12:27301481
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135-656C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301481 | ||||||
| chr12:27301595
|
T | C | 1 | a0001c0001t0003g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.135-542T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301595 | ||||||
| chr12:27301903
|
G | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.135-234G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301903 | ||||||
| chr12:27301917
|
A | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.135-220A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | chr12 | 27301917 | ||||||
| chr12:27302018
|
GT | G | 5 | a0001c0001t0004g0013a0001c0001t0004g0342a0001c0001t0004g0343others(2): Show | 6 | HG01123.hp1 HG01255.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.135-106delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 27302018 | |||||
| chr12:27302204
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186+16A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302204 | ||||||
| chr12:27302234
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.186+46C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302234 | ||||||
| chr12:27302384
|
C | T | 2 | a0001c0001t0005g0011a0001c0001t0005g0125 | 3 | HG02145.hp2 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.186+196C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302384 | ||||||
| chr12:27302509
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(10): Show | 15 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.186+321A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302509 | ||||||
| chr12:27302561
|
C | G | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.186+373C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302561 | ||||||
| chr12:27302615
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG00738.hp2 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+427G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302615 | ||||||
| chr12:27302742
|
C | T | 1 | a0001c0001t0004g0266 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.186+554C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302742 | ||||||
| chr12:27302762
|
T | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | NA18747.hp1 NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.186+574T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302762 | ||||||
| chr12:27302873
|
A | G | 126 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(123): Show | 134 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.186+685A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302873 | ||||||
| chr12:27302918
|
C | T | 1 | a0001c0001t0003g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.186+730C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302918 | ||||||
| chr12:27302945
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.186+757A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27302945 | ||||||
| chr12:27303012
|
TA | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(188): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.186+846delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | |||||
| chr12:27303012
|
TAA | T | 99 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0001g0165others(96): Show | 102 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.186+845_186+846del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | |||||
| chr12:27303012
|
TAAA | T | 21 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(18): Show | 24 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.186+844_186+846del others(3): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27303012 | |||||
| chr12:27303101
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.186+913C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303101 | ||||||
| chr12:27303113
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.186+925G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303113 | ||||||
| chr12:27303125
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.186+937T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303125 | ||||||
| chr12:27303186
|
T | A | 30 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(27): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+998T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303186 | ||||||
| chr12:27303229
|
G | C | 2 | a0001c0001t0011g0043a0001c0001t0011g0049 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.186+1041G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303229 | ||||||
| chr12:27303316
|
T | C | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.186+1128T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303316 | ||||||
| chr12:27303462
|
G | A | 9 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0050others(6): Show | 11 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.186+1274G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303462 | ||||||
| chr12:27303463
|
C | G | 4 | a0001c0001t0006g0040a0001c0001t0008g0128a0001c0001t0008g0280others(1): Show | 4 | HG02809.hp1 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+1275C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303463 | ||||||
| chr12:27303590
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186+1402A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303590 | ||||||
| chr12:27303648
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.186+1460C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303648 | ||||||
| chr12:27303876
|
T | C | 1 | a0001c0001t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.186+1688T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27303876 | ||||||
| chr12:27304091
|
G | C | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.186+1903G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304091 | ||||||
| chr12:27304194
|
G | T | 1 | a0001c0001t0002g0200 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.186+2006G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304194 | ||||||
| chr12:27304250
|
G | A | 2 | a0001c0001t0006g0050a0001c0001t0018g0100 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.186+2062G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304250 | ||||||
| chr12:27304258
|
C | CA | 31 | a0001c0001t0001g0127a0001c0001t0001g0146a0001c0001t0001g0306others(28): Show | 34 | HG00735.hp1 HG01346.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.186+2092dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | |||||
| chr12:27304258
|
C | CAA | 12 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(9): Show | 14 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.186+2091_186+2092d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | |||||
| chr12:27304258
|
CA | C | 65 | a0001c0001t0001g0030a0001c0001t0001g0286a0001c0001t0003g0006others(62): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.186+2092delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304258 | |||||
| chr12:27304289
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(90): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.186+2101A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304289 | ||||||
| chr12:27304384
|
T | C | 30 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(27): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+2196T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304384 | ||||||
| chr12:27304491
|
A | T | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.186+2303A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304491 | ||||||
| chr12:27304890
|
AT | A | 13 | a0001c0001t0001g0035a0001c0001t0006g0005a0001c0001t0006g0010others(10): Show | 15 | HG00639.hp2 HG00738.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+2712delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27304890 | |||||
| chr12:27304916
|
T | C | 20 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(17): Show | 23 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.186+2728T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304916 | ||||||
| chr12:27304982
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.186+2794T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27304982 | ||||||
| chr12:27305033
|
T | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(261): Show | 274 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.186+2845T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305033 | ||||||
| chr12:27305342
|
T | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-2997T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305342 | ||||||
| chr12:27305411
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.187-2928A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305411 | ||||||
| chr12:27305423
|
TA | T | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(124): Show | 135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.187-2910delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27305423 | |||||
| chr12:27305450
|
CTTA | C | 5 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0019others(2): Show | 5 | NA18968.hp2 NA18989.hp1 NA19078.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-2882_187-2880d others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27305450 | |||||
| chr12:27305471
|
A | G | 1 | a0001c0001t0004g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.187-2868A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305471 | ||||||
| chr12:27305627
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-2712C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305627 | ||||||
| chr12:27305666
|
C | T | 114 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(111): Show | 120 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.187-2673C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305666 | ||||||
| chr12:27305680
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.187-2659G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305680 | ||||||
| chr12:27305894
|
A | G | 127 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(124): Show | 135 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.187-2445A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27305894 | ||||||
| chr12:27306064
|
T | A | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.187-2275T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306064 | ||||||
| chr12:27306272
|
A | G | 1 | a0001c0001t0004g0266 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.187-2067A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306272 | ||||||
| chr12:27306353
|
T | TA | 65 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0060others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.187-1977dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306353 | |||||
| chr12:27306354
|
A | T | 1 | a0001c0001t0008g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187-1985A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306354 | ||||||
| chr12:27306427
|
A | G | 1 | a0001c0001t0006g0005 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.187-1912A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306427 | ||||||
| chr12:27306589
|
T | C | 1 | a0001c0001t0003g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.187-1750T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306589 | ||||||
| chr12:27306614
|
T | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.187-1725T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306614 | ||||||
| chr12:27306712
|
T | TCACACAC others(20): Show |
1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187-1627_187-1626i others(29): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306712 | ||||||
| chr12:27306714
|
A | AAC | 14 | a0001c0001t0001g0155a0001c0001t0002g0111a0001c0001t0003g0006others(11): Show | 15 | HG00408.hp2 HG02132.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.187-1587_187-1586d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACAC | 28 | a0001c0001t0002g0209a0001c0001t0002g0221a0001c0001t0003g0007others(25): Show | 30 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.187-1589_187-1586d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACAC | 11 | a0001c0001t0001g0164a0001c0001t0001g0257a0001c0001t0003g0008others(8): Show | 12 | HG00673.hp1 HG02602.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-1591_187-1586d others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(1): Show |
7 | a0001c0001t0001g0166a0001c0001t0001g0254a0001c0001t0001g0285others(4): Show | 7 | HG00408.hp1 HG01099.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-1593_187-1586d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0126a0001c0001t0001g0282others(5): Show | 10 | HG03669.hp2 NA18942.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-1595_187-1586d others(12): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(5): Show |
8 | a0001c0001t0001g0038a0001c0001t0001g0248a0001c0001t0001g0250others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-1597_187-1586d others(14): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(7): Show |
14 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0142others(11): Show | 14 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.187-1599_187-1586d others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(9): Show |
13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0060others(10): Show | 13 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.187-1601_187-1586d others(18): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(11): Show |
11 | a0001c0001t0001g0036a0001c0001t0001g0129a0001c0001t0001g0151others(8): Show | 11 | HG01109.hp2 HG01243.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-1603_187-1586d others(20): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(13): Show |
13 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0133others(10): Show | 13 | HG00438.hp1 HG00733.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.187-1605_187-1586d others(22): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(15): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0001g0132others(4): Show | 7 | HG01928.hp2 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.187-1607_187-1586d others(24): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(17): Show |
6 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0158others(3): Show | 6 | HG01168.hp2 HG02083.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-1609_187-1586d others(26): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(19): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0001g0136others(3): Show | 6 | HG02071.hp1 HG02300.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-1611_187-1586d others(28): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(21): Show |
5 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0162others(2): Show | 5 | HG01069.hp1 HG02148.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-1613_187-1586d others(30): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(23): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0165a0001c0001t0001g0296 | 3 | HG01496.hp1 HG02818.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.187-1615_187-1586d others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(25): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0156 | 2 | HG00738.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.187-1617_187-1586d others(34): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(27): Show |
3 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02015.hp1 NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.187-1619_187-1586d others(36): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | AACACACA others(29): Show |
1 | a0001c0001t0001g0159 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.187-1621_187-1586d others(38): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0233 | 2 | HG03927.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.187-1625_187-1624i others(15): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | ACACACAC others(10): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0288 | 2 | HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.187-1625_187-1624i others(19): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.187-1625_187-1624i others(21): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0148 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.187-1625_187-1624i others(23): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | ACACACAC others(18): Show |
1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.187-1625_187-1624i others(27): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | ACACACAC others(20): Show |
1 | a0001c0001t0012g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187-1625_187-1624i others(29): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
A | C | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187-1625A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306714 | ||||||
| chr12:27306714
|
AAC | A | 89 | a0001c0001t0002g0009a0001c0001t0002g0039a0001c0001t0002g0055others(86): Show | 91 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.187-1587_187-1586d others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
AACAC | A | 38 | a0001c0001t0002g0078a0001c0001t0002g0110a0001c0001t0002g0177others(35): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.187-1589_187-1586d others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
AACACAC | A | 27 | a0001c0001t0002g0001a0001c0001t0002g0104a0001c0001t0002g0105others(24): Show | 31 | HG00597.hp2 HG02004.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.187-1591_187-1586d others(8): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306714
|
AACACACA others(1): Show |
A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0074others(4): Show | 8 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.187-1593_187-1586d others(10): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27306714 | |||||
| chr12:27306740
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0014g0108 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.187-1599C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306740 | ||||||
| chr12:27306750
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.187-1589C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306750 | ||||||
| chr12:27306754
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187-1585T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306754 | ||||||
| chr12:27306887
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.187-1452C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306887 | ||||||
| chr12:27306922
|
G | A | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.187-1417G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27306922 | ||||||
| chr12:27307049
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.187-1290A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307049 | ||||||
| chr12:27307113
|
A | G | 1 | a0001c0001t0003g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187-1226A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307113 | ||||||
| chr12:27307424
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.187-915A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307424 | ||||||
| chr12:27307468
|
T | G | 314 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(311): Show | 328 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.187-871T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307468 | ||||||
| chr12:27307575
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.187-764A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307575 | ||||||
| chr12:27307676
|
C | G | 2 | a0001c0001t0001g0313a0001c0002t0001g0312 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.187-663C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307676 | ||||||
| chr12:27307899
|
A | C | 1 | a0001c0002t0005g0350 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187-440A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307899 | ||||||
| chr12:27307967
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.187-372A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27307967 | ||||||
| chr12:27308077
|
A | C | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-262A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | chr12 | 27308077 | ||||||
| chr12:27308095
|
C | CAT | 173 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(170): Show | 183 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.187-230_187-229dup others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | |||||
| chr12:27308095
|
C | CATAT | 126 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(123): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.187-232_187-229dup others(4): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | |||||
| chr12:27308095
|
C | CATATAT | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | NA18960.hp2 NA19010.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.187-234_187-229dup others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 27308095 | |||||
| chr12:27308857
|
A | AT | 10 | a0001c0001t0006g0005a0001c0001t0006g0010a0001c0001t0006g0040others(7): Show | 12 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.310-257_310-256ins others(1): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308857 | ||||||
| chr12:27308857
|
AAAATATA others(9): Show |
A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.310-242_310-227del others(16): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308857 | |||||
| chr12:27308859
|
A | T | 17 | a0001c0001t0001g0277a0001c0001t0002g0192a0001c0001t0002g0195others(14): Show | 19 | HG00639.hp2 HG01361.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.310-255A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308859 | ||||||
| chr12:27308861
|
T | A | 1 | a0001c0001t0002g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.310-253T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308861 | ||||||
| chr12:27308875
|
AAT | A | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-231_310-230del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308875 | |||||
| chr12:27308889
|
T | C | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.310-225T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308889 | ||||||
| chr12:27308897
|
T | TAAATATA others(24): Show |
1 | a0001c0001t0003g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-196_310-166dup others(31): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308897 | |||||
| chr12:27308921
|
T | TATATATA others(25): Show |
1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.310-182_310-151dup others(32): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308921 | |||||
| chr12:27308926
|
A | G | 94 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(91): Show | 97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.310-188A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308926 | ||||||
| chr12:27308929
|
A | T | 3 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0339 | 4 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-185A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308929 | ||||||
| chr12:27308942
|
T | TATATATA others(11): Show |
1 | a0001c0001t0003g0098 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.310-165_310-164ins others(18): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308942 | |||||
| chr12:27308953
|
C | A | 1 | a0001c0001t0003g0098 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.310-161C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308953 | ||||||
| chr12:27308953
|
CAT | C | 29 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(26): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.310-155_310-154del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 27308953 | |||||
| chr12:27308969
|
T | G | 2 | a0001c0001t0006g0050a0001c0001t0018g0100 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310-145T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308969 | ||||||
| chr12:27308989
|
T | G | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.310-125T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27308989 | ||||||
| chr12:27309051
|
T | C | 345 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(342): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.310-63T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 4/13 | chr12 | 27309051 | ||||||
| chr12:27309242
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.393+45C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309242 | ||||||
| chr12:27309677
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.393+480T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309677 | ||||||
| chr12:27309705
|
T | C | 129 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(126): Show | 134 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.393+508T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309705 | ||||||
| chr12:27309742
|
G | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.393+545G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309742 | ||||||
| chr12:27309814
|
A | G | 315 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(312): Show | 329 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.393+617A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27309814 | ||||||
| chr12:27310182
|
G | C | 2 | a0001c0001t0002g0207a0001c0001t0002g0228 | 2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.393+985G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310182 | ||||||
| chr12:27310229
|
A | G | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.393+1032A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310229 | ||||||
| chr12:27310341
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.393+1144A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310341 | ||||||
| chr12:27310382
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.393+1185C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310382 | ||||||
| chr12:27310510
|
G | A | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+1313G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310510 | ||||||
| chr12:27310513
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.393+1316A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310513 | ||||||
| chr12:27310546
|
G | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(122): Show | 133 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.393+1349G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310546 | ||||||
| chr12:27310546
|
G | T | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | NA19010.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.393+1349G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310546 | ||||||
| chr12:27310568
|
TAAATA | T | 91 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(88): Show | 94 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.393+1374_393+1378d others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27310568 | |||||
| chr12:27310569
|
A | T | 15 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0060others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+1372A>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310569 | ||||||
| chr12:27310683
|
G | C | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02647.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.393+1486G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310683 | ||||||
| chr12:27310763
|
G | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.393+1566G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27310763 | ||||||
| chr12:27311126
|
C | A | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.394-1423C>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311126 | ||||||
| chr12:27311198
|
C | G | 1 | a0001c0001t0003g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.394-1351C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311198 | ||||||
| chr12:27311302
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.394-1247A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311302 | ||||||
| chr12:27311459
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0228 | 2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.394-1090C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311459 | ||||||
| chr12:27311587
|
T | TATAAAAT others(615): Show |
1 | a0001c0001t0017g0276 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.394-775_394-774ins others(622): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | |||||
| chr12:27311587
|
T | TATAAAAT others(633): Show |
1 | a0001c0001t0001g0292 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.394-775_394-774ins others(640): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | |||||
| chr12:27311587
|
T | TATAAAAT others(635): Show |
1 | a0001c0001t0001g0326 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.394-775_394-774ins others(642): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311587 | |||||
| chr12:27311591
|
A | C | 50 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(47): Show | 54 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.394-958A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311591 | ||||||
| chr12:27311597
|
T | C | 2 | a0001c0001t0005g0328a0001c0001t0005g0329 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.394-952T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311597 | ||||||
| chr12:27311710
|
T | G | 3 | a0001c0003t0002g0117a0001c0003t0002g0119a0001c0003t0002g0253 | 3 | HG00735.hp1 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.394-839T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27311710 | ||||||
| chr12:27311745
|
TAA | T | 94 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(91): Show | 97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.394-802_394-801del others(2): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27311745 | |||||
| chr12:27312132
|
GC | G | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-415delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 27312132 | |||||
| chr12:27312159
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0254 | 2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.394-390G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312159 | ||||||
| chr12:27312167
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394-382C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312167 | ||||||
| chr12:27312174
|
C | T | 2 | a0001c0001t0006g0102a0001c0001t0006g0103 | 2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.394-375C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312174 | ||||||
| chr12:27312257
|
G | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(12): Show | 18 | HG00741.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.394-292G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312257 | ||||||
| chr12:27312319
|
G | A | 21 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.394-230G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 5/13 | chr12 | 27312319 | ||||||
| chr12:27312777
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.517+105T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312777 | ||||||
| chr12:27312815
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+143T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312815 | ||||||
| chr12:27312949
|
C | T | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.517+277C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312949 | ||||||
| chr12:27312986
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.517+314C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27312986 | ||||||
| chr12:27313068
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+396G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313068 | ||||||
| chr12:27313173
|
G | A | 2 | a0001c0001t0010g0225a0001c0001t0010g0332 | 2 | NA18946.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.517+501G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313173 | ||||||
| chr12:27313189
|
A | C | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.517+517A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313189 | ||||||
| chr12:27313248
|
C | CA | 17 | a0001c0001t0002g0181a0001c0001t0003g0063a0001c0001t0003g0086others(14): Show | 19 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.517+594dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313248 | |||||
| chr12:27313248
|
CA | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(137): Show | 142 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.517+594delA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313248 | |||||
| chr12:27313266
|
AT | A | 40 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0053others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.517+595delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313266 | ||||||
| chr12:27313267
|
T | A | 1 | a0001c0001t0004g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.517+595T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313267 | ||||||
| chr12:27313365
|
GGTTTT | G | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.517+709_517+713del others(5): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313365 | |||||
| chr12:27313677
|
C | CT | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.518-826dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27313677 | |||||
| chr12:27313813
|
G | C | 115 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(112): Show | 121 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.518-691G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313813 | ||||||
| chr12:27313826
|
T | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.518-678T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27313826 | ||||||
| chr12:27314007
|
T | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(125): Show | 136 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.518-497T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314007 | ||||||
| chr12:27314243
|
A | G | 1 | a0001c0003t0002g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.518-261A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314243 | ||||||
| chr12:27314281
|
A | G | 1 | a0001c0001t0008g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.518-223A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314281 | ||||||
| chr12:27314391
|
A | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-113A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | chr12 | 27314391 | ||||||
| chr12:27314401
|
C | CA | 135 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.518-85dupA | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 27314401 | |||||
| chr12:27315377
|
T | G | 2 | a0001c0001t0006g0005a0001c0001t0006g0050 | 3 | HG02055.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.837+27T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315377 | ||||||
| chr12:27315380
|
A | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(125): Show | 136 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+30A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315380 | ||||||
| chr12:27315573
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0055others(75): Show | 80 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.837+223A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315573 | ||||||
| chr12:27315750
|
T | C | 15 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(12): Show | 17 | HG00642.hp2 HG00673.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.837+400T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315750 | ||||||
| chr12:27315939
|
T | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0308 | 2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.837+589T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27315939 | ||||||
| chr12:27316071
|
C | T | 1 | a0001c0001t0018g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.837+721C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316071 | ||||||
| chr12:27316340
|
C | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.837+990C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316340 | ||||||
| chr12:27316353
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.838-983G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316353 | ||||||
| chr12:27316411
|
AC | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.838-924delC | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316411 | ||||||
| chr12:27316413
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0184a0001c0001t0003g0185 | 3 | HG03017.hp1 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.838-923A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316413 | ||||||
| chr12:27316486
|
G | A | 1 | a0001c0001t0007g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.838-850G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316486 | ||||||
| chr12:27316595
|
A | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(125): Show | 136 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.838-741A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316595 | ||||||
| chr12:27316597
|
A | C | 3 | a0001c0001t0008g0128a0001c0001t0008g0280a0001c0001t0008g0331 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.838-739A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316597 | ||||||
| chr12:27316607
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.838-729C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316607 | ||||||
| chr12:27316648
|
G | C | 94 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(91): Show | 97 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.838-688G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316648 | ||||||
| chr12:27316807
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.838-529C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316807 | ||||||
| chr12:27316858
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.838-478C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27316858 | ||||||
| chr12:27317090
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.838-246C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27317090 | ||||||
| chr12:27317272
|
C | G | 1 | a0001c0001t0005g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-64C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 9/13 | chr12 | 27317272 | ||||||
| chr12:27317556
|
T | C | 20 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.955+103T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317556 | ||||||
| chr12:27317596
|
T | C | 30 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(27): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.955+143T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317596 | ||||||
| chr12:27317749
|
C | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(258): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.956-147C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317749 | ||||||
| chr12:27317855
|
C | T | 41 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0053others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.956-41C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 10/13 | chr12 | 27317855 | ||||||
| chr12:27318108
|
G | A | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | NA19010.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1079+89G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318108 | ||||||
| chr12:27318284
|
G | C | 1 | a0001c0001t0002g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1079+265G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318284 | ||||||
| chr12:27318584
|
C | T | 5 | a0001c0001t0006g0102a0001c0001t0006g0103a0001c0001t0006g0114others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+565C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318584 | ||||||
| chr12:27318729
|
T | C | 353 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(350): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1080-599T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318729 | ||||||
| chr12:27318730
|
G | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1080-598G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318730 | ||||||
| chr12:27318788
|
A | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(125): Show | 136 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1080-540A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318788 | ||||||
| chr12:27318848
|
G | A | 49 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1080-480G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318848 | ||||||
| chr12:27318851
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0002g0116 | 2 | HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1080-477C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318851 | ||||||
| chr12:27318920
|
G | A | 1 | a0001c0001t0003g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1080-408G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318920 | ||||||
| chr12:27318978
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1080-350G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27318978 | ||||||
| chr12:27319022
|
A | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1080-306A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27319022 | ||||||
| chr12:27319161
|
G | A | 16 | a0001c0001t0005g0011a0001c0001t0005g0125a0001c0001t0005g0328others(13): Show | 19 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1080-167G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 11/13 | chr12 | 27319161 | ||||||
| chr12:27319609
|
G | C | 9 | a0001c0001t0003g0006a0001c0001t0003g0045a0001c0001t0003g0046others(6): Show | 10 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175+186G>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319609 | ||||||
| chr12:27319660
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1175+237T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319660 | ||||||
| chr12:27319803
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1175+380C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319803 | ||||||
| chr12:27319986
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1175+563T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27319986 | ||||||
| chr12:27320018
|
T | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(125): Show | 136 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1175+595T>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320018 | ||||||
| chr12:27320178
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1175+755C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320178 | ||||||
| chr12:27320293
|
G | T | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1175+870G>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320293 | ||||||
| chr12:27320353
|
A | C | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0107others(1): Show | 4 | HG02257.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+930A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320353 | ||||||
| chr12:27320384
|
A | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1175+961A>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320384 | ||||||
| chr12:27320442
|
A | AT | 192 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(189): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1175+1041dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | |||||
| chr12:27320442
|
A | ATT | 64 | a0001c0001t0001g0030a0001c0001t0001g0126a0001c0001t0001g0127others(61): Show | 68 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1175+1040_1175+104 others(6): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | |||||
| chr12:27320442
|
A | ATTT | 12 | a0001c0001t0001g0233a0001c0001t0002g0113a0001c0001t0003g0058others(9): Show | 12 | HG00423.hp1 HG02040.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175+1039_1175+104 others(7): Show |
STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | |||||
| chr12:27320442
|
AT | A | 31 | a0001c0001t0004g0002a0001c0001t0004g0053a0001c0001t0004g0054others(28): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175+1041delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320442 | |||||
| chr12:27320445
|
T | A | 1 | a0001c0001t0004g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1175+1022T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320445 | ||||||
| chr12:27320561
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1175+1138G>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320561 | ||||||
| chr12:27320660
|
T | A | 23 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 23 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1175+1237T>A | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320660 | ||||||
| chr12:27320686
|
T | C | 23 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 23 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1175+1263T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320686 | ||||||
| chr12:27320780
|
A | AT | 60 | a0001c0001t0001g0138a0001c0001t0001g0148a0001c0001t0001g0162others(57): Show | 64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1176-1344dupT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320780 | |||||
| chr12:27320780
|
AT | A | 14 | a0001c0001t0001g0133a0001c0001t0002g0104a0001c0001t0002g0105others(11): Show | 15 | HG01361.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176-1344delT | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 27320780 | |||||
| chr12:27320816
|
C | G | 1 | a0001c0001t0002g0219 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1176-1327C>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320816 | ||||||
| chr12:27320939
|
C | T | 1 | a0001c0001t0006g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1176-1204C>T | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320939 | ||||||
| chr12:27320957
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1176-1186A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320957 | ||||||
| chr12:27320984
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18986.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1176-1159T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27320984 | ||||||
| chr12:27321359
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1176-784A>G | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321359 | ||||||
| chr12:27321373
|
T | C | 2 | a0001c0001t0003g0091a0001c0001t0003g0093 | 2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1176-770T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321373 | ||||||
| chr12:27321758
|
T | C | 125 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0039others(122): Show | 133 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.1176-385T>C | STK38L | ENSG00000211455.8 | transcript | ENST00000389032.8 | protein_coding | 12/13 | chr12 | 27321758 |