Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55681 |
|---|---|
| ensemblid | ENSG00000136021.19 |
| hgncid | 19286 |
| symbol | SCYL2 |
| name | SCY1 like pseudokinase 2 |
| refseq_nuc | NM_017988.6 |
| refseq_prot | NP_060458.3 |
| ensembl_nuc | ENST00000360820.7 |
| ensembl_prot | ENSP00000354061.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 100267177 |
| end | 100341715 |
| strand | + |
| ver | v1.2 |
| region | chr12:100267177-100341715 |
| region5000 | chr12:100262177-100346715 |
| regionname0 | SCYL2_chr12_100267177_100341715 |
| regionname5000 | SCYL2_chr12_100262177_100346715 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 929 | 203 | 72 | 36 | 60 | 12 | 22 | 39 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0002 | 0/0 | 929 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0003 | 0/1 | 929 | 3 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0004 | 0/0 | 929 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0005 | 0/0 | 929 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0006 | 0/0 | 929 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0007 | 0/0 | 929 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0008 | 0/0 | 929 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2790 | 141 | 40 | 30 | 49 | 4 | 17 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0002 | 0/0 | 2790 | 24 | 17 | 0 | 3 | 2 | 2 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0003 | 0/0 | 2790 | 17 | 4 | 5 | 1 | 4 | 3 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0004 | 0/0 | 2790 | 8 | 0 | 0 | 8 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0005 | 0/0 | 2790 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0006 | 0/0 | 2790 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0007 | 0/0 | 2790 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0008 | 0/1 | 2790 | 3 | 1 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0009 | 0/0 | 2790 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0010 | 0/0 | 2790 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0011 | 0/0 | 2790 | 2 | 0 | 1 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0012 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0013 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0014 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0015 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0016 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0017 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| c0018 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3188 | 144 | 30 | 30 | 58 | 8 | 16 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0002 | 0/0 | 3188 | 28 | 9 | 5 | 4 | 6 | 4 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0003 | 0/0 | 3183 | 9 | 9 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0004 | 0/0 | 3188 | 9 | 9 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0005 | 0/0 | 3188 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0006 | 0/0 | 3188 | 5 | 5 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0007 | 0/0 | 3188 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0008 | 0/0 | 3188 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0009 | 0/0 | 3188 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0010 | 0/0 | 3188 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0011 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0012 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0013 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0014 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0015 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0016 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0017 | 0/0 | 3188 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| t0018 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2790 | 141 | 40 | 30 | 49 | 4 | 17 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002 | 0/0 | 2790 | 24 | 17 | 0 | 3 | 2 | 2 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0003 | 0/0 | 2790 | 17 | 4 | 5 | 1 | 4 | 3 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0005 | 0/0 | 2790 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0006 | 0/0 | 2790 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0007 | 0/0 | 2790 | 3 | 3 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0009 | 0/0 | 2790 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0010 | 0/0 | 2790 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0016 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0017 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0018 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0002c0004 | 0/0 | 2790 | 8 | 0 | 0 | 8 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0003c0008 | 0/1 | 2790 | 3 | 1 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0004c0011 | 0/0 | 2790 | 2 | 0 | 1 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0005c0015 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0006c0014 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0007c0012 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0008c0013 | 0/0 | 2790 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5977 | 125 | 27 | 28 | 49 | 4 | 16 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0002 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0006 | 0/0 | 5977 | 5 | 5 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0007 | 0/0 | 5977 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0009 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0015 | 0/0 | 5977 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0016 | 0/0 | 5977 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0001t0017 | 0/0 | 5977 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0001 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0002 | 0/0 | 5977 | 7 | 1 | 0 | 3 | 2 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0003 | 0/0 | 5972 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0004 | 0/0 | 5977 | 9 | 9 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0008 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0002t0011 | 0/0 | 5972 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0003t0002 | 0/0 | 5977 | 15 | 2 | 5 | 1 | 4 | 3 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0003t0010 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0005t0005 | 0/0 | 5977 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0006t0003 | 0/0 | 5972 | 4 | 4 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0007t0002 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0007t0013 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0007t0014 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0009t0001 | 0/0 | 5977 | 2 | 0 | 0 | 0 | 2 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0010t0002 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0016t0012 | 0/0 | 5977 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0017t0001 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0001c0018t0003 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0002c0004t0001 | 0/0 | 5977 | 7 | 0 | 0 | 7 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0002c0004t0018 | 0/0 | 5977 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0003c0008t0001 | 0/1 | 5977 | 3 | 1 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0004c0011t0001 | 0/0 | 5977 | 2 | 0 | 1 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0005c0015t0001 | 0/0 | 5977 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0006c0014t0002 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0007c0012t0001 | 0/0 | 5977 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| a0008c0013t0001 | 0/0 | 5977 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | copy fasta | chr12 | 100262177 | 100346715 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0016g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0001t0017g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0002t0011g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0003t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0005t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0006t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0006t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0006t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0007t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0007t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0007t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0010t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0010t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0016t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0017t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0001c0018t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0002c0004t0018g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0003c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0003c0008t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0003c0008t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0004c0011t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0004c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0005c0015t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0006c0014t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0007c0012t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| a0008c0013t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00140 | hp1 | a0004 | c0011 | t0001 | g0098 | EUR | GBR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0170 | EUR | GBR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0181 | EUR | FIN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00280 | hp2 | a0005 | c0015 | t0001 | g0068 | EUR | FIN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00323 | hp1 | a0001 | c0009 | t0001 | g0131 | EUR | FIN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00323 | hp2 | a0001 | c0009 | t0001 | g0081 | EUR | FIN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00544 | hp2 | a0001 | c0005 | t0005 | g0202 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0185 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0177 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0173 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01099 | hp2 | a0001 | c0016 | t0012 | g0174 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0061 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01175 | hp1 | a0003 | c0008 | t0001 | g0101 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0182 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0171 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0175 | EUR | IBS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0108 | EUR | IBS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0109 | EUR | IBS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0180 | EUR | IBS | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01884 | hp2 | a0001 | c0007 | t0014 | g0169 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0172 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02004 | hp1 | a0004 | c0011 | t0001 | g0087 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0088 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0189 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02056 | hp1 | a0001 | c0005 | t0005 | g0204 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02080 | hp2 | a0002 | c0004 | t0001 | g0040 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02451 | hp2 | a0001 | c0007 | t0013 | g0168 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0178 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0183 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02647 | hp1 | a0001 | c0010 | t0002 | g0163 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02647 | hp2 | a0001 | c0017 | t0001 | g0005 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0194 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0176 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0196 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0195 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0191 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02965 | hp1 | a0001 | c0003 | t0010 | g0166 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0207 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0003 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0190 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03195 | hp1 | a0001 | c0006 | t0003 | g0018 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03209 | hp2 | a0001 | c0006 | t0003 | g0003 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03486 | hp1 | a0001 | c0003 | t0010 | g0167 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0192 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03540 | hp1 | a0001 | c0002 | t0008 | g0208 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03579 | hp1 | a0001 | c0018 | t0003 | g0020 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03579 | hp2 | a0001 | c0010 | t0002 | g0164 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03834 | hp1 | a0001 | c0002 | t0011 | g0110 | SAS | BEB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0112 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0179 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG04228 | hp2 | a0001 | c0001 | t0017 | g0158 | SAS | STU | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0193 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18612 | hp2 | a0001 | c0005 | t0005 | g0203 | EAS | CHB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18942 | hp2 | a0001 | c0005 | t0005 | g0198 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18947 | hp2 | a0002 | c0004 | t0018 | g0161 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18960 | hp2 | a0001 | c0005 | t0005 | g0201 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18961 | hp1 | a0002 | c0004 | t0001 | g0041 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18961 | hp2 | a0008 | c0013 | t0001 | g0148 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18971 | hp2 | a0002 | c0004 | t0001 | g0039 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18979 | hp2 | a0007 | c0012 | t0001 | g0147 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18981 | hp1 | a0001 | c0005 | t0005 | g0199 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | LWK | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19043 | hp2 | a0001 | c0007 | t0002 | g0162 | AFR | LWK | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19058 | hp2 | a0002 | c0004 | t0001 | g0160 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0049 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19078 | hp1 | a0001 | c0005 | t0005 | g0200 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0159 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19082 | hp1 | a0002 | c0004 | t0001 | g0021 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0056 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0106 | AFR | YRI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0165 | AFR | ASW | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG03471 | hp2 | a0006 | c0014 | t0002 | g0065 | AFR | MSL | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG06807 | hp1 | a0001 | c0006 | t0003 | g0019 | AFR | USA | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| HG06807 | hp2 | a0003 | c0008 | t0001 | g0086 | AFR | USA | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0197 | AFR | LWK | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0008 | t0001 | g0091 | REF | REF | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0205 | REF | REF | SCYL2_chr12_100262177_100346715 | SCYL2 | chr12 | 100262177 | 100346715 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100312568
|
T | C | 2 | a0007a0008 | 2 | NA18961.hp2 NA18979.hp2 |
missense_variant | MODERATE | c.767T>C | p.Met256Thr | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 6/18 | 1411/5977 | 767/2790 | 256/929 | chr12 | 100312568 | ||
| chr12:100314589
|
C | T | 2 | a0003a0004 | 5 | HG00140.hp1 HG01175.hp1 HG02004.hp1 others(2): Show |
missense_variant | MODERATE | c.1070C>T | p.Pro357Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/18 | 1714/5977 | 1070/2790 | 357/929 | chr12 | 100314589 | ||
| chr12:100326688
|
G | T | 1 | a0008 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.1576G>T | p.Asp526Tyr | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/18 | 2220/5977 | 1576/2790 | 526/929 | chr12 | 100326688 | ||
| chr12:100335868
|
G | A | 1 | a0004 | 2 | HG00140.hp1 HG02004.hp1 |
missense_variant | MODERATE | c.1987G>A | p.Glu663Lys | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/18 | 2631/5977 | 1987/2790 | 663/929 | chr12 | 100335868 | ||
| chr12:100338529
|
C | G | 1 | a0002 | 8 | HG02080.hp2 NA18947.hp2 NA18961.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.2147C>G | p.Thr716Ser | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2791/5977 | 2147/2790 | 716/929 | chr12 | 100338529 | ||
| chr12:100338615
|
A | G | 1 | a0005 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2233A>G | p.Thr745Ala | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2877/5977 | 2233/2790 | 745/929 | chr12 | 100338615 | ||
| chr12:100338978
|
A | G | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2596A>G | p.Asn866Asp | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 3240/5977 | 2596/2790 | 866/929 | chr12 | 100338978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100282997
|
G | A | 1 | a0001c0005 | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
synonymous_variant | LOW | c.27G>A | p.Lys9Lys | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/18 | 671/5977 | 27/2790 | 9/929 | chr12 | 100282997 | ||
| chr12:100313487
|
A | G | 3 | a0001c0006a0001c0017a0001c0018 | 6 | HG02647.hp2 HG02976.hp1 HG03195.hp1 others(3): Show |
synonymous_variant | LOW | c.918A>G | p.Leu306Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/18 | 1562/5977 | 918/2790 | 306/929 | chr12 | 100313487 | ||
| chr12:100315642
|
C | T | 4 | a0001c0003a0001c0007a0001c0010others(1): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
synonymous_variant | LOW | c.1180C>T | p.Leu394Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/18 | 1824/5977 | 1180/2790 | 394/929 | chr12 | 100315642 | ||
| chr12:100317811
|
A | G | 1 | a0001c0007 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1281A>G | p.Leu427Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/18 | 1925/5977 | 1281/2790 | 427/929 | chr12 | 100317811 | ||
| chr12:100317838
|
A | G | 1 | a0001c0009 | 2 | HG00323.hp1 HG00323.hp2 |
synonymous_variant | LOW | c.1308A>G | p.Leu436Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/18 | 1952/5977 | 1308/2790 | 436/929 | chr12 | 100317838 | ||
| chr12:100317904
|
A | G | 1 | a0001c0010 | 2 | HG02647.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1374A>G | p.Glu458Glu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/18 | 2018/5977 | 1374/2790 | 458/929 | chr12 | 100317904 | ||
| chr12:100317919
|
G | A | 1 | a0001c0016 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1389G>A | p.Gln463Gln | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/18 | 2033/5977 | 1389/2790 | 463/929 | chr12 | 100317919 | ||
| chr12:100323534
|
C | T | 1 | a0001c0018 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1405C>T | p.Leu469Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/18 | 2049/5977 | 1405/2790 | 469/929 | chr12 | 100323534 | ||
| chr12:100338549
|
C | T | 8 | a0001c0002a0001c0003a0001c0005others(5): Show | 59 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(56): Show |
synonymous_variant | LOW | c.2167C>T | p.Leu723Leu | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2811/5977 | 2167/2790 | 723/929 | chr12 | 100338549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100267186
|
C | T | 1 | a0001c0003t0010 | 2 | HG02965.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-635C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | 15785 | chr12 | 100267186 | |||||
| chr12:100267229
|
C | T | 1 | a0002c0004t0018 | 1 | NA18947.hp2 | 5_prime_UTR_variant | MODIFIER | c.-592C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | 15742 | chr12 | 100267229 | |||||
| chr12:100267433
|
C | T | 1 | a0001c0001t0006 | 5 | HG02145.hp2 HG02818.hp1 HG03225.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-388C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | 15538 | chr12 | 100267433 | |||||
| chr12:100267440
|
G | C | 17 | a0001c0001t0002a0001c0002t0002a0001c0002t0003others(14): Show | 61 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-381G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | 15531 | chr12 | 100267440 | |||||
| chr12:100267527
|
T | C | 1 | a0001c0001t0015 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-294T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | 15444 | chr12 | 100267527 | |||||
| chr12:100267553
|
C | T | 1 | a0001c0002t0008 | 2 | HG02965.hp2 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-268C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | chr12 | 100267553 | ||||||
| chr12:100267723
|
C | G | 1 | a0001c0002t0004 | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/18 | chr12 | 100267723 | ||||||
| chr12:100339721
|
T | C | 4 | a0001c0002t0003a0001c0002t0004a0001c0006t0003others(1): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 549 | chr12 | 100339721 | |||||
| chr12:100340026
|
A | T | 1 | a0001c0001t0017 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 854 | chr12 | 100340026 | |||||
| chr12:100340399
|
A | G | 1 | a0001c0001t0007 | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1227A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1227 | chr12 | 100340399 | |||||
| chr12:100340671
|
C | T | 1 | a0001c0007t0014 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1499 | chr12 | 100340671 | |||||
| chr12:100340727
|
G | T | 1 | a0001c0005t0005 | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1555G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1555 | chr12 | 100340727 | |||||
| chr12:100340839
|
T | C | 1 | a0001c0001t0016 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1667 | chr12 | 100340839 | |||||
| chr12:100340887
|
A | G | 1 | a0001c0007t0013 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1715 | chr12 | 100340887 | |||||
| chr12:100340958
|
A | T | 1 | a0001c0016t0012 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 1786 | chr12 | 100340958 | |||||
| chr12:100341277
|
A | G | 4 | a0001c0002t0003a0001c0002t0004a0001c0006t0003others(1): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2105A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2105 | chr12 | 100341277 | |||||
| chr12:100341447
|
C | A | 1 | a0001c0001t0009 | 2 | HG02258.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2275C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2275 | chr12 | 100341447 | |||||
| chr12:100341594
|
GTTTTC | G | 4 | a0001c0002t0003a0001c0002t0011a0001c0006t0003others(1): Show | 10 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2427_*2431delCTTT others(1): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 18/18 | 2427 | INFO_REALIGN_3_PRIME | chr12 | 100341594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:100267849
|
C | T | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29+57C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100267849 | ||||||
| chr12:100268023
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-29+231A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268023 | ||||||
| chr12:100268050
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-29+258T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268050 | ||||||
| chr12:100268134
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+342C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268134 | ||||||
| chr12:100268203
|
C | G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+411C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268203 | ||||||
| chr12:100268225
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG00735.hp1 HG01258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+433T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268225 | ||||||
| chr12:100268246
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 6 | NA18981.hp2 NA18983.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+454A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268246 | ||||||
| chr12:100268268
|
C | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+476C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268268 | ||||||
| chr12:100268497
|
A | G | 1 | a0001c0003t0002g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-29+705A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268497 | ||||||
| chr12:100268635
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29+843A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268635 | ||||||
| chr12:100268849
|
A | T | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29+1057A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268849 | ||||||
| chr12:100268859
|
A | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29+1067A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100268859 | ||||||
| chr12:100269242
|
T | G | 1 | a0002c0004t0001g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-29+1450T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100269242 | ||||||
| chr12:100269359
|
C | T | 3 | a0002c0004t0001g0159a0002c0004t0001g0160a0002c0004t0018g0161 | 3 | NA18947.hp2 NA19058.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-29+1567C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100269359 | ||||||
| chr12:100269844
|
G | A | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29+2052G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100269844 | ||||||
| chr12:100269851
|
A | T | 1 | a0001c0001t0017g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-29+2059A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100269851 | ||||||
| chr12:100269984
|
A | T | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-29+2192A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100269984 | ||||||
| chr12:100270009
|
C | T | 1 | a0001c0002t0004g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-29+2217C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270009 | ||||||
| chr12:100270012
|
A | T | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+2220A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270012 | ||||||
| chr12:100270042
|
C | A | 47 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(44): Show | 48 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-29+2250C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270042 | ||||||
| chr12:100270239
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-29+2447G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270239 | ||||||
| chr12:100270266
|
C | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 38 | HG00544.hp1 HG00558.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-29+2474C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270266 | ||||||
| chr12:100270287
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-29+2495G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270287 | ||||||
| chr12:100270333
|
G | A | 1 | a0001c0010t0002g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29+2541G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270333 | ||||||
| chr12:100270349
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-29+2557C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270349 | ||||||
| chr12:100270593
|
C | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+2801C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270593 | ||||||
| chr12:100270623
|
C | CT | 17 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(14): Show | 18 | HG00140.hp2 HG02055.hp2 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29+2848dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100270623 | |||||
| chr12:100270623
|
C | CTT | 25 | a0001c0003t0002g0171a0001c0003t0002g0172a0001c0003t0002g0173others(22): Show | 25 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-29+2847_-29+2848d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100270623 | |||||
| chr12:100270642
|
A | G | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-29+2850A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270642 | ||||||
| chr12:100270694
|
C | T | 5 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+2902C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270694 | ||||||
| chr12:100270695
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG00735.hp1 HG01258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+2903G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270695 | ||||||
| chr12:100270695
|
G | T | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-29+2903G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270695 | ||||||
| chr12:100270742
|
T | G | 2 | a0001c0001t0001g0005a0001c0017t0001g0005 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29+2950T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270742 | ||||||
| chr12:100270931
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-29+3139A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100270931 | ||||||
| chr12:100270948
|
GTTT | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+3160_-29+3162d others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100270948 | |||||
| chr12:100271216
|
G | A | 1 | a0002c0004t0001g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-29+3424G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271216 | ||||||
| chr12:100271260
|
C | CA | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+3490dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100271260 | |||||
| chr12:100271260
|
CA | C | 112 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-29+3490delA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100271260 | |||||
| chr12:100271260
|
CAA | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+3489_-29+3490d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100271260 | |||||
| chr12:100271281
|
A | AAAAG | 16 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(13): Show | 16 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-29+3490_-29+3491i others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100271281 | |||||
| chr12:100271281
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(50): Show | 59 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29+3489A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271281 | ||||||
| chr12:100271682
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-29+3890G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271682 | ||||||
| chr12:100271766
|
ATTC | A | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+3977_-29+3979d others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100271766 | |||||
| chr12:100271916
|
A | G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+4124A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271916 | ||||||
| chr12:100271949
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-29+4157A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271949 | ||||||
| chr12:100271994
|
C | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+4202C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100271994 | ||||||
| chr12:100272036
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-29+4244A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100272036 | ||||||
| chr12:100272147
|
A | C | 5 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0113others(2): Show | 5 | HG02015.hp2 HG02080.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+4355A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100272147 | ||||||
| chr12:100272268
|
C | CT | 29 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0029others(26): Show | 30 | HG00544.hp1 HG00558.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-29+4482dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100272268 | |||||
| chr12:100272392
|
G | A | 4 | a0001c0001t0007g0056a0001c0001t0007g0057a0001c0001t0007g0058others(1): Show | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4600G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100272392 | ||||||
| chr12:100272530
|
C | T | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-29+4738C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100272530 | ||||||
| chr12:100272815
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5023G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100272815 | ||||||
| chr12:100273271
|
A | G | 17 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29+5479A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273271 | ||||||
| chr12:100273378
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+5586C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273378 | ||||||
| chr12:100273428
|
T | G | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-29+5636T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273428 | ||||||
| chr12:100273460
|
T | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5668T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273460 | ||||||
| chr12:100273853
|
A | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+6061A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273853 | ||||||
| chr12:100273854
|
A | G | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+6062A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273854 | ||||||
| chr12:100273865
|
C | G | 3 | a0001c0006t0003g0003a0001c0006t0003g0019a0001c0018t0003g0020 | 4 | HG02976.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+6073C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273865 | ||||||
| chr12:100273895
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(3): Show | 6 | HG00735.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+6103C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273895 | ||||||
| chr12:100273945
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-29+6153T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100273945 | ||||||
| chr12:100274209
|
C | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+6417C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274209 | ||||||
| chr12:100274228
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0054a0001c0001t0001g0055 | 4 | HG02055.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+6436T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274228 | ||||||
| chr12:100274442
|
T | C | 1 | a0001c0001t0016g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-29+6650T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274442 | ||||||
| chr12:100274595
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-29+6803A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274595 | ||||||
| chr12:100274820
|
G | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+7028G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274820 | ||||||
| chr12:100274849
|
A | G | 1 | a0001c0001t0007g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-29+7057A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100274849 | ||||||
| chr12:100275022
|
G | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29+7230G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100275022 | ||||||
| chr12:100275541
|
A | C | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-7402A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100275541 | ||||||
| chr12:100275640
|
C | G | 4 | a0001c0002t0004g0193a0001c0002t0004g0194a0001c0002t0004g0195others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-7303C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100275640 | ||||||
| chr12:100275892
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-28-7051A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100275892 | ||||||
| chr12:100275902
|
GTCAGTTT others(4): Show |
G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-7038_-28-7028d others(13): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100275902 | |||||
| chr12:100276030
|
G | A | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-28-6913G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276030 | ||||||
| chr12:100276090
|
G | T | 2 | a0001c0001t0001g0105a0001c0001t0009g0106 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-28-6853G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276090 | ||||||
| chr12:100276374
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-6569G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276374 | ||||||
| chr12:100276418
|
G | T | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28-6525G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276418 | ||||||
| chr12:100276485
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-6458A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276485 | ||||||
| chr12:100276546
|
C | T | 3 | a0001c0006t0003g0003a0001c0006t0003g0019a0001c0018t0003g0020 | 4 | HG02976.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-6397C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276546 | ||||||
| chr12:100276634
|
T | G | 1 | a0001c0002t0004g0193 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-28-6309T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276634 | ||||||
| chr12:100276890
|
A | G | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-6053A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100276890 | ||||||
| chr12:100277082
|
A | C | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-5861A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277082 | ||||||
| chr12:100277146
|
T | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-5797T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277146 | ||||||
| chr12:100277209
|
A | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-5734A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277209 | ||||||
| chr12:100277265
|
A | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28-5678A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277265 | ||||||
| chr12:100277470
|
T | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-5473T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277470 | ||||||
| chr12:100277538
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-5405A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277538 | ||||||
| chr12:100277869
|
T | C | 2 | a0001c0005t0005g0199a0001c0005t0005g0200 | 2 | NA18981.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-28-5074T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100277869 | ||||||
| chr12:100278123
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-4820C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278123 | ||||||
| chr12:100278124
|
G | A | 17 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-4819G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278124 | ||||||
| chr12:100278212
|
G | T | 57 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-4731G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278212 | ||||||
| chr12:100278320
|
C | G | 1 | a0001c0001t0001g0050 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-28-4623C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278320 | ||||||
| chr12:100278376
|
T | G | 1 | a0001c0007t0013g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-28-4567T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278376 | ||||||
| chr12:100278597
|
G | A | 4 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-4346G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278597 | ||||||
| chr12:100278630
|
CT | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-28-4295delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100278630 | |||||
| chr12:100278692
|
T | C | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-28-4251T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278692 | ||||||
| chr12:100278862
|
T | G | 2 | a0001c0007t0013g0168a0001c0007t0014g0169 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-28-4081T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278862 | ||||||
| chr12:100278907
|
C | T | 1 | a0001c0010t0002g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-28-4036C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100278907 | ||||||
| chr12:100279133
|
G | A | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-28-3810G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279133 | ||||||
| chr12:100279139
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-28-3804G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279139 | ||||||
| chr12:100279143
|
A | G | 2 | a0001c0003t0002g0180a0001c0003t0002g0181 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-28-3800A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279143 | ||||||
| chr12:100279179
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-28-3764G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279179 | ||||||
| chr12:100279866
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-28-3077G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279866 | ||||||
| chr12:100279875
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-28-3068C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279875 | ||||||
| chr12:100279909
|
T | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28-3034T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100279909 | ||||||
| chr12:100280148
|
A | C | 57 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-2795A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280148 | ||||||
| chr12:100280188
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-28-2755G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280188 | ||||||
| chr12:100280192
|
G | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-2751G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280192 | ||||||
| chr12:100280457
|
A | G | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-28-2486A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280457 | ||||||
| chr12:100280649
|
C | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-2294C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280649 | ||||||
| chr12:100280810
|
A | G | 1 | a0001c0002t0003g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-28-2133A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280810 | ||||||
| chr12:100280878
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-28-2065A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280878 | ||||||
| chr12:100280988
|
A | G | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-1955A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100280988 | ||||||
| chr12:100281019
|
G | GT | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(63): Show | 69 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-28-1895dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTT | 17 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 17 | HG00140.hp1 HG01175.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-28-1896_-28-1895d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTGTT others(5): Show |
1 | a0001c0002t0003g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-28-1920_-28-1919i others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTGTT others(6): Show |
1 | a0001c0002t0003g0014 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-28-1920_-28-1919i others(15): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTGTT others(7): Show |
4 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1920_-28-1919i others(16): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTGTT others(12): Show |
1 | a0001c0002t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-28-1920_-28-1919i others(21): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTTTT others(5): Show |
1 | a0001c0005t0005g0201 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-28-1906_-28-1895d others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTTTT others(6): Show |
2 | a0001c0005t0005g0198a0001c0005t0005g0202 | 2 | HG00544.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-28-1907_-28-1895d others(15): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTTTT others(7): Show |
4 | a0001c0002t0003g0016a0001c0005t0005g0199a0001c0005t0005g0200others(1): Show | 4 | NA18612.hp2 NA18981.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1908_-28-1895d others(16): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
G | GTTTTTTT others(13): Show |
1 | a0001c0005t0005g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-1914_-28-1895d others(22): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
GTTTTTTT others(3): Show |
G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-1904_-28-1895d others(12): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281019
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28-1906_-28-1895d others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281019 | |||||
| chr12:100281024
|
T | TTTG | 5 | a0001c0003t0002g0165a0001c0003t0002g0178a0001c0003t0002g0179others(2): Show | 5 | HG02602.hp1 HG02647.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1917_-28-1916i others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281024 | |||||
| chr12:100281025
|
T | TTG | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0175others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-1917_-28-1916i others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281025 | |||||
| chr12:100281026
|
T | TG | 3 | a0001c0003t0002g0172a0001c0003t0002g0173a0001c0003t0002g0182 | 3 | HG01074.hp2 HG01256.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.-28-1917_-28-1916i others(3): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281026 | ||||||
| chr12:100281034
|
T | G | 1 | a0001c0003t0002g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-28-1909T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281034 | ||||||
| chr12:100281239
|
G | A | 4 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1704G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281239 | ||||||
| chr12:100281272
|
A | G | 1 | a0001c0002t0004g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28-1671A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281272 | ||||||
| chr12:100281304
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-1639C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281304 | ||||||
| chr12:100281400
|
A | G | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-1543A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281400 | ||||||
| chr12:100281466
|
G | A | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28-1477G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281466 | ||||||
| chr12:100281571
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-1372C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281571 | ||||||
| chr12:100281630
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-28-1313G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281630 | ||||||
| chr12:100281757
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-1186C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281757 | ||||||
| chr12:100281759
|
G | A | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-1184G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281759 | ||||||
| chr12:100281833
|
C | CA | 4 | a0001c0001t0001g0006a0001c0003t0002g0185a0001c0006t0003g0019others(1): Show | 5 | HG00673.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1093dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281833 | |||||
| chr12:100281833
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0134 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-28-1105_-28-1093d others(15): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281833 | |||||
| chr12:100281841
|
A | AAAG | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-1100_-28-1099i others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100281841 | |||||
| chr12:100281935
|
A | G | 1 | a0003c0008t0001g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-28-1008A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100281935 | ||||||
| chr12:100282058
|
C | T | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-28-885C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282058 | ||||||
| chr12:100282117
|
C | T | 16 | a0001c0001t0001g0133a0001c0002t0003g0014a0001c0002t0003g0015others(13): Show | 17 | HG00544.hp2 HG02056.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-826C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282117 | ||||||
| chr12:100282181
|
TGCCTGGC others(294): Show |
T | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-28-743_-28-443del | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100282181 | |||||
| chr12:100282223
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-28-720C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282223 | ||||||
| chr12:100282227
|
A | G | 26 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(23): Show | 27 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.-28-716A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282227 | ||||||
| chr12:100282319
|
C | CT | 21 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0083others(18): Show | 21 | HG00735.hp2 HG01175.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-600dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 100282319 | |||||
| chr12:100282394
|
T | C | 26 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(23): Show | 27 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.-28-549T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282394 | ||||||
| chr12:100282561
|
G | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-382G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282561 | ||||||
| chr12:100282567
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-376C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282567 | ||||||
| chr12:100282629
|
C | G | 4 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-314C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282629 | ||||||
| chr12:100282772
|
G | A | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-28-171G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282772 | ||||||
| chr12:100282928
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-28-15C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 1/17 | chr12 | 100282928 | ||||||
| chr12:100283182
|
C | A | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.177+35C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283182 | ||||||
| chr12:100283209
|
G | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+62G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283209 | ||||||
| chr12:100283233
|
G | A | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+86G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283233 | ||||||
| chr12:100283269
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.177+122T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283269 | ||||||
| chr12:100283550
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.177+403G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283550 | ||||||
| chr12:100283569
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+422G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283569 | ||||||
| chr12:100283575
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.177+428G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283575 | ||||||
| chr12:100283655
|
G | C | 21 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.177+508G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283655 | ||||||
| chr12:100283947
|
A | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.177+800A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283947 | ||||||
| chr12:100283973
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.177+826A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283973 | ||||||
| chr12:100283999
|
T | A | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.177+852T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100283999 | ||||||
| chr12:100284022
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.177+875T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284022 | ||||||
| chr12:100284460
|
A | G | 1 | a0001c0002t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+1313A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284460 | ||||||
| chr12:100284567
|
A | G | 1 | a0001c0007t0013g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.177+1420A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284567 | ||||||
| chr12:100284752
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.177+1605C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284752 | ||||||
| chr12:100284852
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.177+1705T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284852 | ||||||
| chr12:100284879
|
A | G | 2 | a0002c0004t0001g0041a0002c0004t0001g0049 | 2 | NA18961.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.177+1732A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284879 | ||||||
| chr12:100284889
|
C | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+1742C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284889 | ||||||
| chr12:100284985
|
A | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1838A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100284985 | ||||||
| chr12:100285039
|
T | C | 2 | a0001c0001t0001g0005a0001c0017t0001g0005 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.177+1892T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285039 | ||||||
| chr12:100285092
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.177+1945A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285092 | ||||||
| chr12:100285103
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.177+1956A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285103 | ||||||
| chr12:100285256
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.177+2109A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285256 | ||||||
| chr12:100285338
|
T | A | 1 | a0001c0002t0004g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.177+2191T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285338 | ||||||
| chr12:100285446
|
G | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+2299G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285446 | ||||||
| chr12:100285512
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(27): Show | 31 | HG00544.hp1 HG00558.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.177+2365A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100285512 | ||||||
| chr12:100286053
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+2906G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100286053 | ||||||
| chr12:100286144
|
T | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+2997T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100286144 | ||||||
| chr12:100286543
|
G | T | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.177+3396G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100286543 | ||||||
| chr12:100287184
|
A | G | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.177+4037A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287184 | ||||||
| chr12:100287206
|
T | C | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.177+4059T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287206 | ||||||
| chr12:100287238
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+4091C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287238 | ||||||
| chr12:100287240
|
A | G | 1 | a0001c0003t0002g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.177+4093A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287240 | ||||||
| chr12:100287336
|
G | A | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-4167G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287336 | ||||||
| chr12:100287507
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.178-3996A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287507 | ||||||
| chr12:100287510
|
C | T | 16 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-3993C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287510 | ||||||
| chr12:100287578
|
A | G | 1 | a0001c0003t0010g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.178-3925A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287578 | ||||||
| chr12:100287840
|
A | T | 8 | a0002c0004t0001g0021a0002c0004t0001g0039a0002c0004t0001g0040others(5): Show | 8 | HG02080.hp2 NA18947.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-3663A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100287840 | ||||||
| chr12:100288302
|
G | GT | 7 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0017others(4): Show | 8 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-3192dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 100288302 | |||||
| chr12:100288371
|
C | A | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178-3132C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288371 | ||||||
| chr12:100288407
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-3096C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288407 | ||||||
| chr12:100288682
|
A | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.178-2821A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288682 | ||||||
| chr12:100288729
|
C | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.178-2774C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288729 | ||||||
| chr12:100288844
|
G | GA | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0082others(3): Show | 6 | HG00738.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-2647dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 100288844 | |||||
| chr12:100288908
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.178-2595A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288908 | ||||||
| chr12:100288919
|
C | T | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178-2584C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288919 | ||||||
| chr12:100288982
|
C | T | 3 | a0001c0001t0002g0064a0001c0001t0002g0094a0006c0014t0002g0065 | 3 | HG02615.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.178-2521C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100288982 | ||||||
| chr12:100289055
|
C | T | 1 | a0001c0001t0017g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178-2448C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100289055 | ||||||
| chr12:100289342
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.178-2161A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100289342 | ||||||
| chr12:100289449
|
G | A | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-2054G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100289449 | ||||||
| chr12:100289507
|
A | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-1996A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100289507 | ||||||
| chr12:100289890
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-1613T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100289890 | ||||||
| chr12:100290151
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.178-1352T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290151 | ||||||
| chr12:100290326
|
C | T | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-1177C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290326 | ||||||
| chr12:100290330
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1173G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290330 | ||||||
| chr12:100290412
|
A | G | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-1091A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290412 | ||||||
| chr12:100290529
|
A | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.178-974A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290529 | ||||||
| chr12:100290716
|
A | T | 2 | a0001c0009t0001g0081a0001c0009t0001g0131 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.178-787A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290716 | ||||||
| chr12:100290799
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178-704G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290799 | ||||||
| chr12:100290893
|
G | C | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0011g0110 | 3 | HG01515.hp2 HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.178-610G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100290893 | ||||||
| chr12:100291089
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.178-414C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100291089 | ||||||
| chr12:100291127
|
A | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.178-376A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100291127 | ||||||
| chr12:100291157
|
T | C | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-346T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 2/17 | chr12 | 100291157 | ||||||
| chr12:100291772
|
G | A | 3 | a0001c0006t0003g0003a0001c0006t0003g0019a0001c0018t0003g0020 | 4 | HG02976.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+112G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100291772 | ||||||
| chr12:100291904
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.335+244A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100291904 | ||||||
| chr12:100292074
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.335+414A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100292074 | ||||||
| chr12:100292533
|
G | A | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.335+873G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100292533 | ||||||
| chr12:100292714
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.335+1054G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100292714 | ||||||
| chr12:100292740
|
A | AT | 4 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0151others(1): Show | 4 | HG00738.hp2 HG03491.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+1084dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100292740 | |||||
| chr12:100292811
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.335+1151T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100292811 | ||||||
| chr12:100292850
|
C | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.335+1190C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100292850 | ||||||
| chr12:100293047
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.335+1387G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293047 | ||||||
| chr12:100293067
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.335+1407C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293067 | ||||||
| chr12:100293162
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.335+1502G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293162 | ||||||
| chr12:100293276
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.335+1616A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293276 | ||||||
| chr12:100293458
|
C | T | 24 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(21): Show | 25 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.335+1798C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293458 | ||||||
| chr12:100293519
|
GT | G | 15 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(12): Show | 16 | HG00544.hp2 HG02056.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.335+1869delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100293519 | |||||
| chr12:100293520
|
T | G | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.335+1860T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293520 | ||||||
| chr12:100293529
|
T | A | 1 | a0001c0001t0016g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.335+1869T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293529 | ||||||
| chr12:100293625
|
C | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.335+1965C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293625 | ||||||
| chr12:100293712
|
T | C | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.335+2052T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293712 | ||||||
| chr12:100293714
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.335+2054G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293714 | ||||||
| chr12:100293780
|
G | A | 2 | a0001c0001t0007g0056a0001c0001t0007g0057 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.335+2120G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293780 | ||||||
| chr12:100293783
|
G | T | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.335+2123G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293783 | ||||||
| chr12:100293834
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.335+2174C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100293834 | ||||||
| chr12:100294064
|
G | C | 1 | a0001c0002t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.335+2404G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294064 | ||||||
| chr12:100294102
|
C | T | 4 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+2442C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294102 | ||||||
| chr12:100294106
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.335+2446C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294106 | ||||||
| chr12:100294120
|
C | CCTCACCT others(6): Show |
15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.335+2462_335+2474d others(15): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294120 | |||||
| chr12:100294130
|
C | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.335+2470C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294130 | ||||||
| chr12:100294132
|
G | A | 3 | a0003c0008t0001g0086a0004c0011t0001g0087a0004c0011t0001g0098 | 3 | HG00140.hp1 HG02004.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.335+2472G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294132 | ||||||
| chr12:100294158
|
CTGACTCC others(42): Show |
C | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.335+2503_335+2551d others(51): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294158 | |||||
| chr12:100294161
|
A | AC | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.335+2502dupC | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294161 | |||||
| chr12:100294163
|
T | C | 56 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.335+2503T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294163 | ||||||
| chr12:100294194
|
G | C | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.335+2534G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294194 | ||||||
| chr12:100294201
|
G | C | 21 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.335+2541G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294201 | ||||||
| chr12:100294232
|
T | A | 8 | a0002c0004t0001g0021a0002c0004t0001g0039a0002c0004t0001g0040others(5): Show | 8 | HG02080.hp2 NA18947.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.335+2572T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294232 | ||||||
| chr12:100294246
|
A | G | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.335+2586A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294246 | ||||||
| chr12:100294266
|
A | C | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.335+2606A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294266 | ||||||
| chr12:100294271
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.335+2611C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294271 | ||||||
| chr12:100294278
|
GGACGGGG others(71): Show |
G | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.335+2639_335+2716d others(80): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294278 | |||||
| chr12:100294281
|
C | T | 2 | a0001c0002t0001g0104a0001c0003t0002g0165 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.335+2621C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294281 | ||||||
| chr12:100294342
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0116 | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.335+2682G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294342 | ||||||
| chr12:100294349
|
A | ACCTCCCA others(190): Show |
3 | a0001c0001t0002g0064a0001c0001t0002g0094a0001c0001t0007g0057 | 3 | HG02615.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294349 | |||||
| chr12:100294349
|
A | ACCTCCCA others(141): Show |
1 | a0001c0001t0001g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.335+2715_335+2716i others(150): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294349 | |||||
| chr12:100294358
|
A | G | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+2698A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294358 | ||||||
| chr12:100294365
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.335+2705G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294365 | ||||||
| chr12:100294373
|
G | C | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.335+2713G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294373 | ||||||
| chr12:100294383
|
C | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028 | 3 | HG01884.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.335+2723C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294383 | ||||||
| chr12:100294410
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0002g0064a0001c0001t0002g0094others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.335+2750G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294410 | ||||||
| chr12:100294412
|
G | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(16): Show | 20 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.335+2752G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294412 | ||||||
| chr12:100294414
|
G | A | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.335+2754G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294414 | ||||||
| chr12:100294426
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0002g0064a0001c0001t0002g0094others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.335+2766G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294426 | ||||||
| chr12:100294428
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0002g0064a0001c0001t0002g0094others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.335+2768G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294428 | ||||||
| chr12:100294428
|
G | GGGGCTGA others(141): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028 | 3 | HG01884.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.335+2771_335+2772i others(150): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGGTG others(191): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0120a0001c0001t0001g0136 | 3 | HG00438.hp2 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(200): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGGTG others(192): Show |
1 | a0001c0001t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(201): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGGTG others(193): Show |
1 | a0001c0005t0005g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.335+2772_335+2773i others(202): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGGTG others(192): Show |
1 | a0001c0001t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(201): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGGTG others(193): Show |
1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(202): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(240): Show |
3 | a0001c0006t0003g0003a0001c0006t0003g0019a0001c0018t0003g0020 | 4 | HG02976.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(249): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(289): Show |
4 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(1): Show | 4 | HG02615.hp2 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(298): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
1 | a0001c0010t0002g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(119): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(702): Show |
1 | a0001c0001t0001g0134 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(711): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(141): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0055 | 3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(150): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(288): Show |
1 | a0001c0002t0004g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.335+2772_335+2773i others(297): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(288): Show |
7 | a0001c0002t0004g0190a0001c0002t0004g0191a0001c0002t0004g0192others(4): Show | 7 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(297): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(289): Show |
1 | a0001c0002t0004g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(298): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
29 | a0001c0002t0003g0014a0001c0003t0002g0165a0001c0003t0002g0170others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(191): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0097a0002c0004t0001g0159 | 3 | HG01175.hp2 HG04199.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(200): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
2 | a0002c0004t0001g0041a0002c0004t0001g0049 | 2 | NA18961.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(191): Show |
3 | a0001c0001t0001g0130a0001c0001t0016g0061a0003c0008t0001g0101 | 3 | HG00741.hp1 HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(200): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(142): Show |
1 | a0001c0001t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.335+2772_335+2773i others(151): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(191): Show |
1 | a0001c0003t0002g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.335+2772_335+2773i others(200): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(140): Show |
8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+2772_335+2773i others(149): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294428
|
G | GGGGGTGA others(190): Show |
2 | a0001c0009t0001g0081a0001c0009t0001g0131 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.335+2772_335+2773i others(199): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294428 | |||||
| chr12:100294440
|
C | G | 1 | a0001c0001t0001g0048 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.335+2780C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294440 | ||||||
| chr12:100294458
|
C | T | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2798C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294458 | ||||||
| chr12:100294482
|
A | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2822A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294482 | ||||||
| chr12:100294483
|
G | A | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2823G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294483 | ||||||
| chr12:100294486
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2826T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294486 | ||||||
| chr12:100294500
|
A | G | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2840A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294500 | ||||||
| chr12:100294507
|
GGGCTGAC others(7): Show |
G | 41 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.335+2862_335+2875d others(16): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294507 | |||||
| chr12:100294515
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2855T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294515 | ||||||
| chr12:100294521
|
A | ACCTCCCT others(127): Show |
9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.335+2861_335+2862i others(136): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294521 | ||||||
| chr12:100294521
|
A | ACCTCCCT others(128): Show |
1 | a0001c0002t0003g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.335+2861_335+2862i others(137): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294521 | ||||||
| chr12:100294521
|
A | ACCTCCCT others(127): Show |
6 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0006t0003g0003others(3): Show | 7 | HG02976.hp1 HG03139.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.335+2861_335+2862i others(136): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294521 | ||||||
| chr12:100294529
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2869T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294529 | ||||||
| chr12:100294546
|
A | G | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2886A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294546 | ||||||
| chr12:100294550
|
C | G | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2890C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294550 | ||||||
| chr12:100294550
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG00735.hp1 HG01258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.335+2890C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294550 | ||||||
| chr12:100294551
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.335+2891G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294551 | ||||||
| chr12:100294566
|
C | CG | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2911dupG | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294566 | |||||
| chr12:100294575
|
A | AC | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2921dupC | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294575 | |||||
| chr12:100294592
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2932T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294592 | ||||||
| chr12:100294597
|
A | G | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2937A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294597 | ||||||
| chr12:100294598
|
G | A | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2938G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294598 | ||||||
| chr12:100294601
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2941T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294601 | ||||||
| chr12:100294610
|
G | A | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.335+2950G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294610 | ||||||
| chr12:100294621
|
C | T | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.335+2961C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294621 | ||||||
| chr12:100294642
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0002g0064others(55): Show | 59 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(56): Show |
intron_variant | MODIFIER | c.335+2982T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294642 | ||||||
| chr12:100294646
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2986T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294646 | ||||||
| chr12:100294657
|
A | G | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+2997A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294657 | ||||||
| chr12:100294670
|
C | A | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3010C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294670 | ||||||
| chr12:100294674
|
C | T | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3014C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294674 | ||||||
| chr12:100294679
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3019T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294679 | ||||||
| chr12:100294688
|
G | A | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3028G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294688 | ||||||
| chr12:100294691
|
CGGGGGGC others(42): Show |
C | 2 | a0001c0002t0003g0014a0001c0003t0002g0172 | 2 | HG01928.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.335+3068_335+3116d others(51): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294691 | |||||
| chr12:100294703
|
C | T | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3043C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294703 | ||||||
| chr12:100294713
|
C | CCCTCCCA others(118): Show |
16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3059_335+3060i others(127): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294713 | |||||
| chr12:100294720
|
G | A | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.335+3060G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294720 | ||||||
| chr12:100294728
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(173): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.335+3068T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294728 | ||||||
| chr12:100294736
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.335+3076C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294736 | ||||||
| chr12:100294740
|
T | C | 16 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(13): Show | 17 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+3080T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294740 | ||||||
| chr12:100294768
|
C | T | 2 | a0001c0001t0001g0120a0002c0004t0001g0021 | 2 | HG01169.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.335+3108C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294768 | ||||||
| chr12:100294776
|
G | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.335+3116G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294776 | ||||||
| chr12:100294777
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.335+3117C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294777 | ||||||
| chr12:100294789
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.335+3129C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294789 | ||||||
| chr12:100294801
|
C | T | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.335+3141C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294801 | ||||||
| chr12:100294818
|
G | C | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.335+3158G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294818 | ||||||
| chr12:100294818
|
G | GGACGGGG others(33): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG00735.hp1 HG01258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.335+3173_336-3159d others(42): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294818 | |||||
| chr12:100294818
|
GGACGGGG others(33): Show |
G | 1 | a0001c0003t0002g0180 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.335+3173_336-3159d others(42): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100294818 | |||||
| chr12:100294833
|
T | C | 48 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(45): Show | 49 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.335+3173T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294833 | ||||||
| chr12:100294840
|
A | C | 14 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.335+3180A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294840 | ||||||
| chr12:100294844
|
G | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.335+3184G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294844 | ||||||
| chr12:100294873
|
C | T | 2 | a0001c0009t0001g0081a0001c0009t0001g0131 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.336-3158C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294873 | ||||||
| chr12:100294902
|
G | A | 4 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-3129G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294902 | ||||||
| chr12:100294906
|
C | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.336-3125C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294906 | ||||||
| chr12:100294918
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.336-3113G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294918 | ||||||
| chr12:100294941
|
C | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.336-3090C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294941 | ||||||
| chr12:100294941
|
C | T | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.336-3090C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100294941 | ||||||
| chr12:100295009
|
C | A | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0011g0110 | 3 | HG01515.hp2 HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.336-3022C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295009 | ||||||
| chr12:100295018
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.336-3013C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295018 | ||||||
| chr12:100295047
|
C | G | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.336-2984C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295047 | ||||||
| chr12:100295048
|
A | C | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.336-2983A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295048 | ||||||
| chr12:100295066
|
C | T | 5 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-2965C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295066 | ||||||
| chr12:100295156
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.336-2875C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295156 | ||||||
| chr12:100295251
|
C | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.336-2780C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295251 | ||||||
| chr12:100295273
|
G | A | 1 | a0001c0002t0004g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.336-2758G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295273 | ||||||
| chr12:100295303
|
G | A | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-2728G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295303 | ||||||
| chr12:100295374
|
C | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.336-2657C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295374 | ||||||
| chr12:100295408
|
A | G | 1 | a0001c0002t0003g0014 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.336-2623A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295408 | ||||||
| chr12:100295425
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.336-2606C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295425 | ||||||
| chr12:100295426
|
G | A | 1 | a0001c0002t0004g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.336-2605G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295426 | ||||||
| chr12:100295450
|
C | T | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.336-2581C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295450 | ||||||
| chr12:100295452
|
T | C | 22 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(19): Show | 22 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.336-2579T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295452 | ||||||
| chr12:100295592
|
G | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0151others(1): Show | 4 | HG00738.hp2 HG03491.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.336-2439G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295592 | ||||||
| chr12:100295629
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.336-2402A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295629 | ||||||
| chr12:100295656
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.336-2375C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295656 | ||||||
| chr12:100295673
|
TGAGAGGG others(18): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.336-2341_336-2317d others(27): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100295673 | |||||
| chr12:100295770
|
CGGGAGA | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.336-2235_336-2230d others(8): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 100295770 | |||||
| chr12:100295799
|
G | C | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.336-2232G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295799 | ||||||
| chr12:100295867
|
G | T | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.336-2164G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295867 | ||||||
| chr12:100295883
|
C | T | 8 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-2148C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100295883 | ||||||
| chr12:100296360
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.336-1671A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100296360 | ||||||
| chr12:100296534
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.336-1497A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100296534 | ||||||
| chr12:100296587
|
A | G | 3 | a0001c0001t0002g0064a0001c0001t0002g0094a0006c0014t0002g0065 | 3 | HG02615.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.336-1444A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100296587 | ||||||
| chr12:100296591
|
A | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.336-1440A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100296591 | ||||||
| chr12:100296911
|
T | A | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-1120T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100296911 | ||||||
| chr12:100297089
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.336-942G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297089 | ||||||
| chr12:100297255
|
A | G | 1 | a0001c0002t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.336-776A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297255 | ||||||
| chr12:100297318
|
ACAGCACA others(9): Show |
A | 4 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114others(1): Show | 4 | HG02015.hp2 HG02080.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.336-712_336-697del others(16): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297318 | ||||||
| chr12:100297336
|
GGGAC | G | 4 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114others(1): Show | 4 | HG02015.hp2 HG02080.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.336-694_336-691del others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297336 | ||||||
| chr12:100297554
|
A | G | 1 | a0001c0002t0004g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.336-477A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297554 | ||||||
| chr12:100297558
|
G | A | 1 | a0001c0001t0006g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.336-473G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297558 | ||||||
| chr12:100297607
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.336-424A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297607 | ||||||
| chr12:100297749
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0094a0006c0014t0002g0065 | 3 | HG02615.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.336-282G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297749 | ||||||
| chr12:100297871
|
T | A | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.336-160T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100297871 | ||||||
| chr12:100298012
|
T | A | 1 | a0001c0005t0005g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.336-19T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 3/17 | chr12 | 100298012 | ||||||
| chr12:100298462
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.480+287A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298462 | ||||||
| chr12:100298571
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.480+396C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298571 | ||||||
| chr12:100298572
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0082others(3): Show | 6 | HG00738.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+397G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298572 | ||||||
| chr12:100298606
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.480+431A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298606 | ||||||
| chr12:100298635
|
C | T | 1 | a0001c0003t0010g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.480+460C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298635 | ||||||
| chr12:100298637
|
C | CCTCCCTG others(10): Show |
7 | a0001c0001t0002g0064a0001c0001t0002g0094a0001c0001t0007g0056others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+474_480+490dup others(17): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100298637 | |||||
| chr12:100298857
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.480+682C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100298857 | ||||||
| chr12:100299096
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(27): Show | 31 | HG00544.hp1 HG00558.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.480+921A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299096 | ||||||
| chr12:100299239
|
AAAC | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(3): Show | 7 | NA18950.hp1 NA18966.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+1079_480+1081d others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100299239 | |||||
| chr12:100299272
|
T | C | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.480+1097T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299272 | ||||||
| chr12:100299273
|
G | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.480+1098G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299273 | ||||||
| chr12:100299291
|
A | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.480+1116A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299291 | ||||||
| chr12:100299336
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.480+1161G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299336 | ||||||
| chr12:100299458
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.480+1283T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299458 | ||||||
| chr12:100299627
|
T | A | 17 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.480+1452T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299627 | ||||||
| chr12:100299656
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.480+1481A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299656 | ||||||
| chr12:100299820
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.480+1645C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299820 | ||||||
| chr12:100299946
|
A | G | 1 | a0001c0002t0002g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.480+1771A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100299946 | ||||||
| chr12:100300043
|
A | T | 3 | a0001c0001t0001g0133a0001c0009t0001g0081a0001c0009t0001g0131 | 3 | HG00323.hp1 HG00323.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.480+1868A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300043 | ||||||
| chr12:100300189
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.480+2014C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300189 | ||||||
| chr12:100300341
|
C | A | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.480+2166C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300341 | ||||||
| chr12:100300615
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.480+2440A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300615 | ||||||
| chr12:100300868
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0044 | 2 | NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.480+2693T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300868 | ||||||
| chr12:100300983
|
C | T | 1 | a0001c0003t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.480+2808C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100300983 | ||||||
| chr12:100301127
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.480+2952G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100301127 | ||||||
| chr12:100301485
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.480+3310C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100301485 | ||||||
| chr12:100301491
|
G | C | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.480+3316G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100301491 | ||||||
| chr12:100301502
|
G | A | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.480+3327G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100301502 | ||||||
| chr12:100302303
|
A | C | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+4128A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100302303 | ||||||
| chr12:100302466
|
C | T | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.480+4291C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100302466 | ||||||
| chr12:100302475
|
T | C | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+4300T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100302475 | ||||||
| chr12:100302747
|
A | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+4572A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100302747 | ||||||
| chr12:100302916
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.480+4741A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100302916 | ||||||
| chr12:100303023
|
T | G | 3 | a0001c0007t0002g0162a0001c0007t0013g0168a0001c0007t0014g0169 | 3 | HG01884.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.480+4848T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303023 | ||||||
| chr12:100303038
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.480+4863C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303038 | ||||||
| chr12:100303251
|
A | G | 1 | a0001c0002t0003g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.480+5076A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303251 | ||||||
| chr12:100303359
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(163): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.480+5184A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303359 | ||||||
| chr12:100303418
|
T | C | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.480+5243T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303418 | ||||||
| chr12:100303607
|
T | C | 14 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.480+5432T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303607 | ||||||
| chr12:100303726
|
G | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.480+5551G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303726 | ||||||
| chr12:100303763
|
G | C | 1 | a0001c0001t0006g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.480+5588G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303763 | ||||||
| chr12:100303801
|
G | A | 1 | a0001c0002t0002g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.480+5626G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303801 | ||||||
| chr12:100303877
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0116 | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+5702A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303877 | ||||||
| chr12:100303988
|
T | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+5813T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100303988 | ||||||
| chr12:100304277
|
G | A | 4 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+6102G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304277 | ||||||
| chr12:100304342
|
A | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+6167A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304342 | ||||||
| chr12:100304368
|
C | T | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.480+6193C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304368 | ||||||
| chr12:100304483
|
G | A | 1 | a0001c0003t0010g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.480+6308G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304483 | ||||||
| chr12:100304560
|
G | A | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.480+6385G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304560 | ||||||
| chr12:100304666
|
G | A | 1 | a0002c0004t0001g0039 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.481-6378G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304666 | ||||||
| chr12:100304716
|
G | A | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-6328G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304716 | ||||||
| chr12:100304741
|
T | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.481-6303T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304741 | ||||||
| chr12:100304829
|
A | C | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-6215A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100304829 | ||||||
| chr12:100305068
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.481-5976G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100305068 | ||||||
| chr12:100305235
|
A | C | 3 | a0001c0002t0004g0190a0001c0002t0004g0191a0001c0002t0004g0192 | 3 | HG02922.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.481-5809A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100305235 | ||||||
| chr12:100305306
|
C | T | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-5738C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100305306 | ||||||
| chr12:100305716
|
G | GT | 13 | a0001c0001t0001g0026a0001c0001t0001g0073a0001c0001t0001g0082others(10): Show | 13 | HG00738.hp1 HG00738.hp2 HG03130.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-5307dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100305716 | |||||
| chr12:100305716
|
GT | G | 4 | a0001c0002t0003g0016a0001c0006t0003g0003a0001c0006t0003g0018others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-5307delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100305716 | |||||
| chr12:100305716
|
GTT | G | 27 | a0001c0001t0001g0072a0001c0002t0002g0112a0001c0002t0008g0207others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.481-5308_481-5307d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100305716 | |||||
| chr12:100305716
|
GTTT | G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-5309_481-5307d others(5): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100305716 | |||||
| chr12:100305716
|
GTTTT | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-5310_481-5307d others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100305716 | |||||
| chr12:100305752
|
T | C | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.481-5292T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100305752 | ||||||
| chr12:100305857
|
A | G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-5187A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100305857 | ||||||
| chr12:100306028
|
G | A | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-5016G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306028 | ||||||
| chr12:100306036
|
C | T | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-5008C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306036 | ||||||
| chr12:100306306
|
T | C | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.481-4738T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306306 | ||||||
| chr12:100306315
|
C | T | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.481-4729C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306315 | ||||||
| chr12:100306661
|
A | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-4383A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306661 | ||||||
| chr12:100306715
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.481-4329T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306715 | ||||||
| chr12:100306752
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-4292C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306752 | ||||||
| chr12:100306853
|
GACAA | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-4187_481-4184d others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100306853 | |||||
| chr12:100306905
|
G | A | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.481-4139G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100306905 | ||||||
| chr12:100307113
|
C | T | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.481-3931C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307113 | ||||||
| chr12:100307297
|
C | T | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.481-3747C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307297 | ||||||
| chr12:100307347
|
T | A | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.481-3697T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307347 | ||||||
| chr12:100307660
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.481-3384A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307660 | ||||||
| chr12:100307702
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-3342C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307702 | ||||||
| chr12:100307737
|
T | C | 1 | a0001c0001t0015g0088 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.481-3307T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307737 | ||||||
| chr12:100307825
|
C | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-3219C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307825 | ||||||
| chr12:100307826
|
G | A | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-3218G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307826 | ||||||
| chr12:100307966
|
A | G | 1 | a0002c0004t0018g0161 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.481-3078A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100307966 | ||||||
| chr12:100308061
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.481-2983A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308061 | ||||||
| chr12:100308088
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481-2956C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308088 | ||||||
| chr12:100308140
|
A | G | 1 | a0005c0015t0001g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.481-2904A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308140 | ||||||
| chr12:100308284
|
A | G | 1 | a0001c0003t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.481-2760A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308284 | ||||||
| chr12:100308364
|
A | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-2680A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308364 | ||||||
| chr12:100308377
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.481-2667T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308377 | ||||||
| chr12:100308395
|
C | T | 17 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.481-2649C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308395 | ||||||
| chr12:100308402
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.481-2642C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308402 | ||||||
| chr12:100308404
|
G | A | 8 | a0001c0001t0001g0103a0001c0005t0005g0198a0001c0005t0005g0199others(5): Show | 8 | HG00544.hp2 HG02056.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-2640G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100308404 | ||||||
| chr12:100309024
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481-2020G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309024 | ||||||
| chr12:100309096
|
G | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(196): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.481-1948G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309096 | ||||||
| chr12:100309106
|
T | TTG | 17 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0054others(14): Show | 18 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.481-1911_481-1910d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
T | TTGTG | 6 | a0001c0001t0001g0184a0001c0003t0002g0165a0001c0003t0002g0180others(3): Show | 6 | HG01516.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-1913_481-1910d others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
T | TTGTGTG | 11 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-1915_481-1910d others(8): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
T | TTGTGTGT others(1): Show |
3 | a0001c0003t0002g0175a0001c0003t0002g0179a0001c0003t0002g0185 | 3 | HG00673.hp1 HG01515.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.481-1917_481-1910d others(10): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
TTG | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG00735.hp1 HG01258.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-1911_481-1910d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
TTGTG | T | 4 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0002t0002g0108others(1): Show | 4 | HG01515.hp2 HG01516.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-1913_481-1910d others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309106
|
TTGTGTG | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1915_481-1910d others(8): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309106 | |||||
| chr12:100309131
|
T | C | 4 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114others(1): Show | 4 | HG02015.hp2 HG02080.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1913T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309131 | ||||||
| chr12:100309133
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0116others(15): Show | 20 | HG00099.hp1 HG00544.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.481-1911T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309133 | ||||||
| chr12:100309133
|
T | TGTGTGTG others(5): Show |
1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.481-1910_481-1909i others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100309133 | |||||
| chr12:100309136
|
G | A | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-1908G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309136 | ||||||
| chr12:100309179
|
G | T | 2 | a0004c0011t0001g0087a0004c0011t0001g0098 | 2 | HG00140.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.481-1865G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309179 | ||||||
| chr12:100309181
|
A | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.481-1863A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309181 | ||||||
| chr12:100309267
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1777C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309267 | ||||||
| chr12:100309269
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.481-1775T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309269 | ||||||
| chr12:100309385
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.481-1659C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309385 | ||||||
| chr12:100309420
|
G | A | 4 | a0001c0001t0007g0056a0001c0001t0007g0057a0001c0001t0007g0058others(1): Show | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1624G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309420 | ||||||
| chr12:100309518
|
G | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1526G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309518 | ||||||
| chr12:100309621
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-1423A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309621 | ||||||
| chr12:100309755
|
C | T | 1 | a0001c0002t0004g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.481-1289C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100309755 | ||||||
| chr12:100310006
|
G | GT | 6 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0201others(3): Show | 6 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1029dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100310006 | |||||
| chr12:100310006
|
G | GTT | 18 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(15): Show | 19 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-1030_481-1029d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 100310006 | |||||
| chr12:100310033
|
G | C | 24 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(21): Show | 25 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1011G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310033 | ||||||
| chr12:100310156
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0105a0001c0001t0009g0007 | 3 | HG02258.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.481-888G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310156 | ||||||
| chr12:100310231
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481-813T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310231 | ||||||
| chr12:100310695
|
G | C | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-349G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310695 | ||||||
| chr12:100310844
|
A | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-200A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310844 | ||||||
| chr12:100310955
|
G | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0130 | 3 | HG00741.hp1 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.481-89G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 4/17 | chr12 | 100310955 | ||||||
| chr12:100311433
|
G | GT | 9 | a0001c0001t0001g0078a0001c0005t0005g0198a0001c0005t0005g0199others(6): Show | 9 | HG00544.hp2 HG01099.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+251dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 100311433 | |||||
| chr12:100311562
|
A | G | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.630+369A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100311562 | ||||||
| chr12:100311657
|
C | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+464C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100311657 | ||||||
| chr12:100311849
|
G | A | 23 | a0001c0003t0002g0165a0001c0003t0002g0170a0001c0003t0002g0171others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.631-583G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100311849 | ||||||
| chr12:100312071
|
A | G | 4 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-361A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100312071 | ||||||
| chr12:100312115
|
T | A | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.631-317T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100312115 | ||||||
| chr12:100312118
|
C | CG | 2 | a0001c0001t0001g0005a0001c0017t0001g0005 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.631-314_631-313ins others(1): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100312118 | ||||||
| chr12:100312119
|
T | C | 2 | a0001c0001t0001g0005a0001c0017t0001g0005 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.631-313T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100312119 | ||||||
| chr12:100312309
|
A | G | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.631-123A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 5/17 | chr12 | 100312309 | ||||||
| chr12:100312838
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.852+185C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 6/17 | chr12 | 100312838 | ||||||
| chr12:100313741
|
C | T | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.969+203C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100313741 | ||||||
| chr12:100313755
|
C | T | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.969+217C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100313755 | ||||||
| chr12:100313880
|
A | AT | 5 | a0001c0001t0001g0055a0001c0001t0001g0146a0001c0007t0013g0168others(2): Show | 5 | HG01884.hp2 HG01928.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+361dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 100313880 | |||||
| chr12:100313886
|
T | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 40 | HG00544.hp1 HG00558.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.969+348T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100313886 | ||||||
| chr12:100314099
|
T | G | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.970-390T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100314099 | ||||||
| chr12:100314171
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.970-318C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100314171 | ||||||
| chr12:100314276
|
C | T | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.970-213C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 7/17 | chr12 | 100314276 | ||||||
| chr12:100314667
|
T | A | 3 | a0001c0002t0004g0190a0001c0002t0004g0191a0001c0002t0004g0192 | 3 | HG02922.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1095+53T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100314667 | ||||||
| chr12:100314749
|
A | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1095+135A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100314749 | ||||||
| chr12:100314802
|
G | C | 1 | a0001c0007t0013g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1095+188G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100314802 | ||||||
| chr12:100314905
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+291A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100314905 | ||||||
| chr12:100314930
|
A | C | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1095+316A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100314930 | ||||||
| chr12:100315036
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1095+422C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315036 | ||||||
| chr12:100315176
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1096-382C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315176 | ||||||
| chr12:100315285
|
C | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1096-273C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315285 | ||||||
| chr12:100315345
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1096-213C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315345 | ||||||
| chr12:100315365
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-193C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315365 | ||||||
| chr12:100315535
|
T | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0062others(38): Show | 42 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1096-23T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315535 | ||||||
| chr12:100315536
|
A | T | 5 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(2): Show | 6 | HG02647.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-22A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 8/17 | chr12 | 100315536 | ||||||
| chr12:100315762
|
ATCTACTG others(11): Show |
A | 6 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0177others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272+30_1272+47del others(18): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 100315762 | |||||
| chr12:100315839
|
G | A | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1272+105G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100315839 | ||||||
| chr12:100316001
|
GTTCT | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1272+270_1272+273d others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 100316001 | |||||
| chr12:100316286
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1272+552A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316286 | ||||||
| chr12:100316358
|
TACTTGAA others(5): Show |
T | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1272+630_1272+641d others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 100316358 | |||||
| chr12:100316380
|
G | A | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+646G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316380 | ||||||
| chr12:100316424
|
G | C | 1 | a0001c0003t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1272+690G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316424 | ||||||
| chr12:100316480
|
G | C | 24 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(21): Show | 25 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.1272+746G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316480 | ||||||
| chr12:100316594
|
G | A | 1 | a0001c0003t0002g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1272+860G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316594 | ||||||
| chr12:100316839
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1273-964C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316839 | ||||||
| chr12:100316940
|
A | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00735.hp1 HG01258.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273-863A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316940 | ||||||
| chr12:100316948
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1273-855C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100316948 | ||||||
| chr12:100317125
|
C | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273-678C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317125 | ||||||
| chr12:100317320
|
C | T | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1273-483C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317320 | ||||||
| chr12:100317528
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0062others(13): Show | 17 | HG01070.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273-275G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317528 | ||||||
| chr12:100317669
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1273-134C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317669 | ||||||
| chr12:100317675
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1273-128A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317675 | ||||||
| chr12:100317755
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1273-48C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 9/17 | chr12 | 100317755 | ||||||
| chr12:100318036
|
A | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0127 | 2 | NA18964.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1395+111A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318036 | ||||||
| chr12:100318165
|
A | T | 25 | a0001c0002t0008g0207a0001c0002t0008g0208a0001c0003t0002g0165others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1395+240A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318165 | ||||||
| chr12:100318270
|
T | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1395+345T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318270 | ||||||
| chr12:100318279
|
A | T | 25 | a0001c0002t0008g0207a0001c0002t0008g0208a0001c0003t0002g0165others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1395+354A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318279 | ||||||
| chr12:100318329
|
C | CT | 31 | a0001c0001t0001g0010a0001c0001t0001g0137a0001c0001t0001g0149others(28): Show | 33 | HG00438.hp1 HG00735.hp2 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1395+423dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100318329 | |||||
| chr12:100318329
|
CT | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0128others(3): Show | 6 | HG01099.hp2 HG01515.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395+423delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100318329 | |||||
| chr12:100318333
|
T | C | 7 | a0001c0001t0002g0064a0001c0001t0002g0094a0001c0001t0007g0056others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+408T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318333 | ||||||
| chr12:100318370
|
G | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(27): Show | 31 | HG00544.hp1 HG00558.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1395+445G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318370 | ||||||
| chr12:100318371
|
C | T | 3 | a0001c0001t0002g0064a0001c0001t0002g0094a0006c0014t0002g0065 | 3 | HG02615.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1395+446C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318371 | ||||||
| chr12:100318528
|
C | T | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395+603C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318528 | ||||||
| chr12:100318564
|
T | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0151others(1): Show | 4 | HG00738.hp2 HG03491.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+639T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318564 | ||||||
| chr12:100318620
|
T | C | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1395+695T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318620 | ||||||
| chr12:100318827
|
T | G | 1 | a0001c0002t0002g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1395+902T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318827 | ||||||
| chr12:100318907
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02523.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1395+982T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318907 | ||||||
| chr12:100318981
|
T | C | 25 | a0001c0002t0008g0207a0001c0002t0008g0208a0001c0003t0002g0165others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1395+1056T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100318981 | ||||||
| chr12:100319324
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1395+1399A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319324 | ||||||
| chr12:100319335
|
T | C | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1395+1410T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319335 | ||||||
| chr12:100319379
|
T | C | 1 | a0001c0005t0005g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1395+1454T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319379 | ||||||
| chr12:100319399
|
A | T | 1 | a0001c0003t0010g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1395+1474A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319399 | ||||||
| chr12:100319447
|
T | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1395+1522T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319447 | ||||||
| chr12:100319626
|
T | A | 4 | a0001c0001t0007g0056a0001c0001t0007g0057a0001c0001t0007g0058others(1): Show | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+1701T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100319626 | ||||||
| chr12:100320272
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1395+2347C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320272 | ||||||
| chr12:100320462
|
G | T | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1395+2537G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320462 | ||||||
| chr12:100320526
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1395+2601C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320526 | ||||||
| chr12:100320542
|
C | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2617C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320542 | ||||||
| chr12:100320544
|
T | C | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395+2619T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320544 | ||||||
| chr12:100320549
|
A | AAAAT | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.1395+2668_1395+267 others(8): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
A | AAAATAAA others(1): Show |
25 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0053others(22): Show | 26 | HG00438.hp1 HG00738.hp1 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.1395+2664_1395+267 others(12): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
AAAAT | A | 17 | a0001c0001t0001g0038a0001c0001t0001g0129a0001c0003t0002g0170others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1395+2668_1395+267 others(8): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0002t0003g0014others(4): Show | 7 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+2664_1395+267 others(12): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
AAAATAAA others(5): Show |
A | 8 | a0001c0001t0001g0074a0001c0002t0002g0108a0001c0002t0002g0109others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395+2660_1395+267 others(16): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
AAAATAAA others(13): Show |
A | 2 | a0001c0001t0007g0056a0001c0001t0007g0057 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1395+2652_1395+267 others(24): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320549
|
AAAATAAA others(17): Show |
A | 2 | a0001c0001t0007g0058a0001c0001t0007g0059 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+2648_1395+267 others(28): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320549 | |||||
| chr12:100320620
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1395+2695G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320620 | ||||||
| chr12:100320725
|
A | G | 22 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(19): Show | 22 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1395+2800A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320725 | ||||||
| chr12:100320781
|
T | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1396-2744T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100320781 | ||||||
| chr12:100320829
|
GGGAACAT others(1): Show |
G | 13 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0033others(10): Show | 13 | HG00558.hp1 HG01261.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1396-2686_1396-267 others(12): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100320829 | |||||
| chr12:100321024
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0017t0001g0005 | 3 | HG02647.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1396-2501G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321024 | ||||||
| chr12:100321206
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1396-2319G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321206 | ||||||
| chr12:100321233
|
T | A | 4 | a0001c0001t0007g0056a0001c0001t0007g0057a0001c0001t0007g0058others(1): Show | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2292T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321233 | ||||||
| chr12:100321659
|
G | T | 25 | a0001c0002t0008g0207a0001c0002t0008g0208a0001c0003t0002g0165others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1396-1866G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321659 | ||||||
| chr12:100321708
|
T | A | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1396-1817T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321708 | ||||||
| chr12:100321783
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1396-1742C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100321783 | ||||||
| chr12:100322044
|
CA | C | 44 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0017others(41): Show | 45 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1396-1465delA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322044 | |||||
| chr12:100322060
|
A | G | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1396-1465A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322060 | ||||||
| chr12:100322061
|
G | A | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1396-1464G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322061 | ||||||
| chr12:100322065
|
A | G | 8 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-1460A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322065 | ||||||
| chr12:100322110
|
C | T | 1 | a0001c0003t0002g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1396-1415C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322110 | ||||||
| chr12:100322111
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1396-1414G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322111 | ||||||
| chr12:100322143
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1396-1382C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322143 | ||||||
| chr12:100322162
|
G | C | 1 | a0001c0002t0002g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1396-1363G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322162 | ||||||
| chr12:100322232
|
G | T | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1396-1293G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322232 | ||||||
| chr12:100322261
|
T | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1264T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322261 | ||||||
| chr12:100322261
|
TAC | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-1263_1396-126 others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322261 | ||||||
| chr12:100322305
|
G | A | 1 | a0001c0005t0005g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396-1220G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322305 | ||||||
| chr12:100322327
|
C | T | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1198C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322327 | ||||||
| chr12:100322368
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1157G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322368 | ||||||
| chr12:100322372
|
C | CA | 12 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0089others(9): Show | 12 | HG00099.hp2 HG01175.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-1132dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322372 | |||||
| chr12:100322372
|
CA | C | 34 | a0001c0001t0001g0096a0001c0001t0002g0064a0001c0001t0002g0094others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1396-1132delA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322372 | |||||
| chr12:100322372
|
CAA | C | 16 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(13): Show | 17 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1396-1133_1396-113 others(6): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322372 | |||||
| chr12:100322475
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1050G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322475 | ||||||
| chr12:100322612
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1396-913C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322612 | ||||||
| chr12:100322675
|
A | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1396-850A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322675 | ||||||
| chr12:100322856
|
G | A | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1396-669G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322856 | ||||||
| chr12:100322860
|
C | CA | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0149others(3): Show | 6 | HG00735.hp2 HG01515.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-647dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322860 | |||||
| chr12:100322860
|
CA | C | 13 | a0001c0001t0001g0129a0001c0002t0002g0112a0001c0002t0002g0113others(10): Show | 13 | HG00544.hp2 HG02015.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.1396-647delA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 100322860 | |||||
| chr12:100322904
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1396-621T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100322904 | ||||||
| chr12:100323049
|
A | G | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1396-476A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100323049 | ||||||
| chr12:100323263
|
G | A | 1 | a0001c0006t0003g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1396-262G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100323263 | ||||||
| chr12:100323482
|
A | T | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1396-43A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100323482 | ||||||
| chr12:100323520
|
T | G | 24 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(21): Show | 25 | HG00544.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.1396-5T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 10/17 | chr12 | 100323520 | ||||||
| chr12:100323946
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+308G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100323946 | ||||||
| chr12:100324052
|
C | T | 4 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+414C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324052 | ||||||
| chr12:100324166
|
A | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+528A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324166 | ||||||
| chr12:100324397
|
A | G | 3 | a0001c0006t0003g0003a0001c0006t0003g0019a0001c0018t0003g0020 | 4 | HG02976.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+759A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324397 | ||||||
| chr12:100324416
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1509+778C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324416 | ||||||
| chr12:100324594
|
G | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+956G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324594 | ||||||
| chr12:100324735
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1509+1097G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324735 | ||||||
| chr12:100324766
|
G | C | 2 | a0001c0003t0010g0166a0001c0003t0010g0167 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1509+1128G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324766 | ||||||
| chr12:100324952
|
C | T | 1 | a0001c0001t0017g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1509+1314C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100324952 | ||||||
| chr12:100325127
|
G | T | 1 | a0001c0003t0002g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1509+1489G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325127 | ||||||
| chr12:100325495
|
C | G | 1 | a0008c0013t0001g0148 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1510-1127C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325495 | ||||||
| chr12:100325555
|
T | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(3): Show | 6 | HG00735.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-1067T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325555 | ||||||
| chr12:100325606
|
T | C | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1510-1016T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325606 | ||||||
| chr12:100325669
|
G | A | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1510-953G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325669 | ||||||
| chr12:100325803
|
T | G | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1510-819T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325803 | ||||||
| chr12:100325819
|
G | A | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1510-803G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100325819 | ||||||
| chr12:100326009
|
A | G | 1 | a0001c0003t0002g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1510-613A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100326009 | ||||||
| chr12:100326263
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1510-359A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100326263 | ||||||
| chr12:100326504
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510-118A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 11/17 | chr12 | 100326504 | ||||||
| chr12:100326839
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1642+85G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100326839 | ||||||
| chr12:100327263
|
T | C | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1642+509T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327263 | ||||||
| chr12:100327356
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1642+602C>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327356 | ||||||
| chr12:100327518
|
A | AT | 5 | a0001c0002t0008g0207a0001c0006t0003g0003a0001c0006t0003g0018others(2): Show | 6 | HG02965.hp2 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1642+778dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 100327518 | |||||
| chr12:100327670
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1642+916C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327670 | ||||||
| chr12:100327739
|
C | G | 6 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0125others(3): Show | 6 | HG00438.hp1 HG02027.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1642+985C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327739 | ||||||
| chr12:100327791
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1642+1037G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327791 | ||||||
| chr12:100327795
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1642+1041G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327795 | ||||||
| chr12:100327851
|
C | G | 4 | a0001c0006t0003g0003a0001c0006t0003g0018a0001c0006t0003g0019others(1): Show | 5 | HG02976.hp1 HG03195.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1642+1097C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100327851 | ||||||
| chr12:100328005
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1643-1196C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328005 | ||||||
| chr12:100328013
|
G | A | 4 | a0001c0002t0004g0193a0001c0002t0004g0194a0001c0002t0004g0195others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1643-1188G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328013 | ||||||
| chr12:100328191
|
T | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(1): Show | 4 | HG00735.hp2 HG01346.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1643-1010T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328191 | ||||||
| chr12:100328277
|
T | TA | 49 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1643-915dupA | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr12 | 100328277 | |||||
| chr12:100328320
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1643-881T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328320 | ||||||
| chr12:100328544
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1643-657G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328544 | ||||||
| chr12:100328660
|
G | T | 1 | a0001c0003t0010g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1643-541G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328660 | ||||||
| chr12:100328833
|
A | G | 1 | a0001c0003t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1643-368A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100328833 | ||||||
| chr12:100329196
|
A | G | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.1643-5A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 12/17 | chr12 | 100329196 | ||||||
| chr12:100329642
|
A | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(3): Show | 6 | HG00735.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761+323A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100329642 | ||||||
| chr12:100329814
|
G | T | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1761+495G>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100329814 | ||||||
| chr12:100329845
|
G | C | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1761+526G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100329845 | ||||||
| chr12:100330169
|
A | T | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1761+850A>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330169 | ||||||
| chr12:100330386
|
T | G | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1761+1067T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330386 | ||||||
| chr12:100330474
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(3): Show | 7 | NA18950.hp1 NA18966.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.1761+1155A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330474 | ||||||
| chr12:100330715
|
T | A | 5 | a0001c0001t0001g0037a0001c0002t0002g0111a0001c0002t0002g0112others(2): Show | 5 | HG02015.hp2 HG02080.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+1396T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330715 | ||||||
| chr12:100330736
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1761+1417G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330736 | ||||||
| chr12:100330830
|
CT | C | 50 | a0001c0001t0001g0186a0001c0001t0002g0064a0001c0001t0002g0094others(47): Show | 51 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(48): Show |
intron_variant | MODIFIER | c.1761+1527delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 100330830 | |||||
| chr12:100330987
|
C | G | 1 | a0001c0002t0003g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1761+1668C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100330987 | ||||||
| chr12:100331379
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1761+2060A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331379 | ||||||
| chr12:100331484
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1761+2165G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331484 | ||||||
| chr12:100331622
|
ATGT | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1761+2307_1761+230 others(7): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 100331622 | |||||
| chr12:100331660
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1761+2341T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331660 | ||||||
| chr12:100331687
|
C | T | 8 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761+2368C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331687 | ||||||
| chr12:100331772
|
G | C | 1 | a0001c0002t0008g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1762-2394G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331772 | ||||||
| chr12:100331863
|
A | C | 8 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-2303A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331863 | ||||||
| chr12:100331899
|
C | G | 1 | a0001c0002t0002g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1762-2267C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331899 | ||||||
| chr12:100331905
|
C | T | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1762-2261C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100331905 | ||||||
| chr12:100332074
|
G | A | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1762-2092G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332074 | ||||||
| chr12:100332199
|
A | G | 15 | a0001c0003t0002g0170a0001c0003t0002g0171a0001c0003t0002g0172others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1762-1967A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332199 | ||||||
| chr12:100332294
|
A | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1762-1872A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332294 | ||||||
| chr12:100332296
|
G | A | 58 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0002g0109others(55): Show | 59 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1762-1870G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332296 | ||||||
| chr12:100332438
|
G | A | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1762-1728G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332438 | ||||||
| chr12:100332444
|
A | C | 5 | a0001c0001t0001g0090a0001c0001t0006g0154a0001c0001t0006g0155others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1762-1722A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332444 | ||||||
| chr12:100332659
|
G | A | 1 | a0001c0001t0006g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1762-1507G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332659 | ||||||
| chr12:100332685
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0116 | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1762-1481C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100332685 | ||||||
| chr12:100332718
|
G | GT | 26 | a0001c0001t0001g0123a0001c0002t0002g0112a0001c0002t0002g0114others(23): Show | 26 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1762-1434dupT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 100332718 | |||||
| chr12:100332718
|
GT | G | 8 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-1434delT | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 100332718 | |||||
| chr12:100333119
|
T | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1762-1047T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333119 | ||||||
| chr12:100333320
|
G | A | 1 | a0001c0001t0007g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1762-846G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333320 | ||||||
| chr12:100333383
|
T | A | 1 | a0001c0007t0002g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1762-783T>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333383 | ||||||
| chr12:100333716
|
T | C | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1762-450T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333716 | ||||||
| chr12:100333722
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1762-444T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333722 | ||||||
| chr12:100333757
|
G | A | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1762-409G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100333757 | ||||||
| chr12:100334036
|
C | T | 1 | a0001c0002t0002g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1762-130C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100334036 | ||||||
| chr12:100334128
|
T | C | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1762-38T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 13/17 | chr12 | 100334128 | ||||||
| chr12:100334594
|
C | G | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1862+328C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100334594 | ||||||
| chr12:100334829
|
C | T | 1 | a0001c0003t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1862+563C>T | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100334829 | ||||||
| chr12:100335035
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1863-590G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100335035 | ||||||
| chr12:100335083
|
T | C | 7 | a0001c0005t0005g0198a0001c0005t0005g0199a0001c0005t0005g0200others(4): Show | 7 | HG00544.hp2 HG02056.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1863-542T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100335083 | ||||||
| chr12:100335371
|
TTGACTGG others(5): Show |
T | 4 | a0001c0001t0007g0056a0001c0001t0007g0057a0001c0001t0007g0058others(1): Show | 4 | HG02486.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1863-249_1863-238d others(14): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 100335371 | |||||
| chr12:100335407
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1863-218G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100335407 | ||||||
| chr12:100335471
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0045 | 2 | HG02027.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1863-154G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 14/17 | chr12 | 100335471 | ||||||
| chr12:100335706
|
A | G | 2 | a0001c0010t0002g0163a0001c0010t0002g0164 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1929+15A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 15/17 | chr12 | 100335706 | ||||||
| chr12:100336081
|
A | G | 17 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2025+175A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100336081 | ||||||
| chr12:100336221
|
T | C | 1 | a0001c0007t0014g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2025+315T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100336221 | ||||||
| chr12:100336414
|
C | CCA | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2025+509_2025+510d others(4): Show |
SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 100336414 | |||||
| chr12:100336635
|
G | C | 8 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0111others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2025+729G>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100336635 | ||||||
| chr12:100336992
|
C | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2026-395C>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100336992 | ||||||
| chr12:100337029
|
A | G | 2 | a0001c0001t0001g0005a0001c0017t0001g0005 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2026-358A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100337029 | ||||||
| chr12:100337238
|
A | C | 1 | a0001c0002t0008g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2026-149A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100337238 | ||||||
| chr12:100337256
|
A | G | 9 | a0001c0002t0004g0189a0001c0002t0004g0190a0001c0002t0004g0191others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2026-131A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100337256 | ||||||
| chr12:100337313
|
G | A | 1 | a0001c0003t0010g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2026-74G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 16/17 | chr12 | 100337313 | ||||||
| chr12:100337950
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0078others(7): Show | 11 | HG01070.hp1 HG01099.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.2145+444T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100337950 | ||||||
| chr12:100337993
|
T | G | 1 | a0001c0002t0004g0193 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2145+487T>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100337993 | ||||||
| chr12:100338001
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2145+495G>A | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338001 | ||||||
| chr12:100338052
|
A | C | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2146-476A>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338052 | ||||||
| chr12:100338085
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(5): Show | 9 | HG02257.hp1 HG02615.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2146-443A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338085 | ||||||
| chr12:100338105
|
T | C | 1 | a0001c0001t0015g0088 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2146-423T>C | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338105 | ||||||
| chr12:100338153
|
A | G | 2 | a0001c0002t0008g0207a0001c0002t0008g0208 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2146-375A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338153 | ||||||
| chr12:100338347
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2146-181A>G | SCYL2 | ENSG00000136021.19 | transcript | ENST00000360820.7 | protein_coding | 17/17 | chr12 | 100338347 |