| geneid | 23256 |
|---|---|
| ensemblid | ENSG00000092108.22 |
| hgncid | 20726 |
| symbol | SCFD1 |
| name | sec1 family domain containing 1 |
| refseq_nuc | NM_016106.4 |
| refseq_prot | NP_057190.2 |
| ensembl_nuc | ENST00000458591.7 |
| ensembl_prot | ENSP00000390783.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 30622319 |
| end | 30735850 |
| strand | + |
| ver | v1.2 |
| region | chr14:30622319-30735850 |
| region5000 | chr14:30617319-30740850 |
| regionname0 | SCFD1_chr14_30622319_30735850 |
| regionname5000 | SCFD1_chr14_30617319_30740850 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 642 | 200 | 62 | 27 | 92 | 3 | 16 | 73 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0002 | 1/1 | 642 | 120 | 20 | 29 | 50 | 5 | 14 | 41 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0003 | 0/0 | 643 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0004 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0005 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0006 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1929 | 193 | 60 | 27 | 89 | 3 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0002 | 1/1 | 1929 | 115 | 20 | 29 | 45 | 5 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0003 | 0/0 | 1929 | 5 | 0 | 0 | 5 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0004 | 0/0 | 1932 | 3 | 3 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0005 | 0/0 | 1932 | 2 | 2 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0006 | 0/0 | 1929 | 2 | 0 | 0 | 0 | 0 | 2 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0007 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0008 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0009 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0010 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0011 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0012 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0013 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| c0014 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 262 | 323 | 83 | 56 | 144 | 8 | 30 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| t0002 | 0/0 | 262 | 5 | 5 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1929 | 193 | 60 | 27 | 89 | 3 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0006 | 0/0 | 1929 | 2 | 0 | 0 | 0 | 0 | 2 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0010 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0011 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0012 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0013 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0014 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0002c0002 | 1/1 | 1929 | 115 | 20 | 29 | 45 | 5 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0002c0003 | 0/0 | 1929 | 5 | 0 | 0 | 5 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0003c0004 | 0/0 | 1932 | 3 | 3 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0003c0005 | 0/0 | 1932 | 2 | 2 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0004c0007 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0005c0009 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0006c0008 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2190 | 193 | 60 | 27 | 89 | 3 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0006t0001 | 0/0 | 2190 | 2 | 0 | 0 | 0 | 0 | 2 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0010t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0011t0001 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0012t0001 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0013t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0001c0014t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0002c0002t0001 | 1/1 | 2190 | 115 | 20 | 29 | 45 | 5 | 14 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0002c0003t0001 | 0/0 | 2190 | 5 | 0 | 0 | 5 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0003c0004t0002 | 0/0 | 2193 | 3 | 3 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0003c0005t0002 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0004c0007t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0005c0009t0001 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| a0006c0008t0001 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | copy fasta | chr14 | 30617319 | 30740850 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0010t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0011t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0012t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0013t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0001c0014t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0003c0004t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0003c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0003c0004t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0003c0005t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0003c0005t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0004c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0005c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| a0006c0008t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0263 | EUR | GBR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0302 | EUR | GBR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0322 | EUR | FIN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0325 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0318 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0319 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0310 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0320 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0305 | AMR | CLM | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01884 | hp1 | a0001 | c0011 | t0001 | g0036 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | CDX | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02258 | hp2 | a0003 | c0005 | t0002 | g0146 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0326 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02818 | hp2 | a0003 | c0004 | t0002 | g0148 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02886 | hp2 | a0001 | c0012 | t0001 | g0210 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02965 | hp2 | a0003 | c0004 | t0002 | g0150 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03017 | hp1 | a0001 | c0006 | t0001 | g0073 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03453 | hp2 | a0006 | c0008 | t0001 | g0056 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0306 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0324 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0297 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0260 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0221 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04199 | hp2 | a0001 | c0006 | t0001 | g0092 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0296 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0226 | SAS | STU | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | CHB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18941 | hp1 | a0001 | c0014 | t0001 | g0133 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18967 | hp1 | a0004 | c0007 | t0001 | g0252 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18970 | hp1 | a0001 | c0010 | t0001 | g0051 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18978 | hp2 | a0005 | c0009 | t0001 | g0117 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18979 | hp1 | a0001 | c0013 | t0001 | g0102 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19030 | hp2 | a0003 | c0004 | t0002 | g0149 | AFR | LWK | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | LWK | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA19240 | hp2 | a0003 | c0005 | t0002 | g0147 | AFR | YRI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ASW | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ASW | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0267 | EUR | TSI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0311 | EUR | TSI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0304 | SAS | GIH | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | USA | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0236 | REF | REF | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0237 | REF | REF | SCFD1_chr14_30617319_30740850 | SCFD1 | chr14 | 30617319 | 30740850 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:30622360
|
A | ACAG | 1 | a0003 | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.36_38dupAGC | p.Ala13dup | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/25 | 59/2190 | 39/1929 | 13/642 | INFO_REALIGN_3_PRIME | chr14 | 30622360 | |
| chr14:30630532
|
A | G | 4 | a0001a0003a0005others(1): Show | 207 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(204): Show |
missense_variant | MODERATE | c.188A>G | p.Lys63Arg | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/25 | 208/2190 | 188/1929 | 63/642 | chr14 | 30630532 | ||
| chr14:30639813
|
G | A | 1 | a0006 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.472G>A | p.Asp158Asn | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/25 | 492/2190 | 472/1929 | 158/642 | chr14 | 30639813 | ||
| chr14:30639846
|
G | C | 1 | a0005 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.505G>C | p.Glu169Gln | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/25 | 525/2190 | 505/1929 | 169/642 | chr14 | 30639846 | ||
| chr14:30674986
|
C | T | 1 | a0004 | 1 | NA18967.hp1 | missense_variant&splice_region_variant | MODERATE | c.1163C>T | p.Ser388Phe | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/25 | 1183/2190 | 1163/1929 | 388/642 | chr14 | 30674986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:30638142
|
A | G | 1 | a0001c0014 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.330A>G | p.Leu110Leu | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/25 | 350/2190 | 330/1929 | 110/642 | chr14 | 30638142 | ||
| chr14:30643368
|
T | C | 1 | a0001c0010 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.576T>C | p.Thr192Thr | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/25 | 596/2190 | 576/1929 | 192/642 | chr14 | 30643368 | ||
| chr14:30670300
|
G | A | 1 | a0001c0006 | 2 | HG03017.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.900G>A | p.Val300Val | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/25 | 920/2190 | 900/1929 | 300/642 | chr14 | 30670300 | ||
| chr14:30670381
|
A | G | 1 | a0003c0005 | 2 | HG02258.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.981A>G | p.Gln327Gln | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/25 | 1001/2190 | 981/1929 | 327/642 | chr14 | 30670381 | ||
| chr14:30673260
|
A | G | 1 | a0001c0013 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.999A>G | p.Pro333Pro | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/25 | 1019/2190 | 999/1929 | 333/642 | chr14 | 30673260 | ||
| chr14:30673293
|
A | G | 1 | a0001c0012 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1032A>G | p.Glu344Glu | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/25 | 1052/2190 | 1032/1929 | 344/642 | chr14 | 30673293 | ||
| chr14:30675020
|
T | A | 1 | a0002c0003 | 5 | NA18948.hp1 NA18954.hp1 NA18959.hp2 others(2): Show |
synonymous_variant | LOW | c.1197T>A | p.Ile399Ile | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/25 | 1217/2190 | 1197/1929 | 399/642 | chr14 | 30675020 | ||
| chr14:30702358
|
A | G | 1 | a0001c0011 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1473A>G | p.Gln491Gln | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/25 | 1493/2190 | 1473/1929 | 491/642 | chr14 | 30702358 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:30735632
|
A | G | 2 | a0003c0004t0002a0003c0005t0002 | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*23A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 25/25 | 23 | chr14 | 30735632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:30622466
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.61+67C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622466 | ||||||
| chr14:30622552
|
T | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.61+153T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622552 | ||||||
| chr14:30622625
|
G | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+226G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622625 | ||||||
| chr14:30622741
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.61+342G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622741 | ||||||
| chr14:30622885
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.61+486G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622885 | ||||||
| chr14:30622966
|
T | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.61+567T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30622966 | ||||||
| chr14:30623021
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.61+622A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623021 | ||||||
| chr14:30623154
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0012t0001g0210 | 3 | HG02886.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.61+755A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623154 | ||||||
| chr14:30623155
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.61+756C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623155 | ||||||
| chr14:30623399
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+1000A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623399 | ||||||
| chr14:30623427
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.61+1028A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623427 | ||||||
| chr14:30623672
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61+1273G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623672 | ||||||
| chr14:30623731
|
G | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.61+1332G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623731 | ||||||
| chr14:30623829
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.61+1430G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30623829 | ||||||
| chr14:30624026
|
T | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.61+1627T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624026 | ||||||
| chr14:30624155
|
C | G | 1 | a0002c0002t0001g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61+1756C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624155 | ||||||
| chr14:30624363
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+1964T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624363 | ||||||
| chr14:30624461
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.61+2062G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624461 | ||||||
| chr14:30624476
|
A | C | 1 | a0002c0002t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.61+2077A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624476 | ||||||
| chr14:30624629
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.61+2230T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624629 | ||||||
| chr14:30624773
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.61+2374T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624773 | ||||||
| chr14:30624974
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.61+2575T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30624974 | ||||||
| chr14:30625071
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+2672T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625071 | ||||||
| chr14:30625227
|
G | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.61+2828G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625227 | ||||||
| chr14:30625230
|
T | TAGTA | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(192): Show |
intron_variant | MODIFIER | c.61+2834_61+2835ins others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625230 | |||||
| chr14:30625274
|
G | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0151a0001c0001t0001g0152others(15): Show | 18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+2875G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625274 | ||||||
| chr14:30625309
|
C | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.62-2900C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625309 | ||||||
| chr14:30625418
|
G | T | 1 | a0002c0002t0001g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-2791G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625418 | ||||||
| chr14:30625546
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.62-2663G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625546 | ||||||
| chr14:30625584
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-2625A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625584 | ||||||
| chr14:30625599
|
TTATAGGT others(13): Show |
T | 6 | a0002c0002t0001g0318a0002c0002t0001g0319a0002c0002t0001g0320others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-2593_62-2574del others(20): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625599 | |||||
| chr14:30625605
|
G | GTATAGGT others(29): Show |
1 | a0002c0002t0001g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.62-2533_62-2498dup others(36): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625605
|
G | GTATAGGT others(9): Show |
39 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0098others(36): Show | 39 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.62-2594_62-2593ins others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625605
|
G | GTATAGGT others(45): Show |
73 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 73 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.62-2594_62-2593ins others(52): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625605
|
G | GTATAGGT others(81): Show |
14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG01074.hp1 HG01099.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-2594_62-2593ins others(88): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625605
|
G | GTATAGGT others(117): Show |
1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62-2594_62-2593ins others(124): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625605
|
GTATAGGT others(29): Show |
G | 1 | a0002c0002t0001g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.62-2533_62-2498del others(36): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625605 | |||||
| chr14:30625688
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-2521C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625688 | ||||||
| chr14:30625712
|
T | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 94 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.62-2497T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625712 | ||||||
| chr14:30625719
|
GTA | G | 123 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(120): Show | 123 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-2485_62-2484del others(2): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625719 | |||||
| chr14:30625721
|
A | ATACCTAT others(19): Show |
1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62-2486_62-2485ins others(26): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625721 | |||||
| chr14:30625721
|
A | ATACCTAT others(135): Show |
10 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0020others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2486_62-2485ins others(142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625721 | |||||
| chr14:30625721
|
A | ATACCTAT others(99): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0208others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-2486_62-2485ins others(106): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625721 | |||||
| chr14:30625721
|
A | ATACCTAT others(63): Show |
71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 72 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.62-2486_62-2485ins others(70): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625721 | |||||
| chr14:30625721
|
A | ATACCTAT others(27): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0098others(2): Show | 5 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-2486_62-2485ins others(34): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30625721 | |||||
| chr14:30625927
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.62-2282A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30625927 | ||||||
| chr14:30626101
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-2108C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626101 | ||||||
| chr14:30626336
|
C | G | 151 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 151 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.62-1873C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626336 | ||||||
| chr14:30626349
|
T | A | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02129.hp2 HG02523.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-1860T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626349 | ||||||
| chr14:30626529
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.62-1680A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626529 | ||||||
| chr14:30626682
|
C | T | 2 | a0002c0002t0001g0315a0002c0002t0001g0316 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.62-1527C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626682 | ||||||
| chr14:30626732
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-1477C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626732 | ||||||
| chr14:30626783
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-1426A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626783 | ||||||
| chr14:30626835
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62-1374A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626835 | ||||||
| chr14:30626938
|
T | G | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(4): Show | 7 | HG00544.hp2 NA18612.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-1271T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626938 | ||||||
| chr14:30626988
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.62-1221C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30626988 | ||||||
| chr14:30627009
|
G | A | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.62-1200G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627009 | ||||||
| chr14:30627039
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.62-1170T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627039 | ||||||
| chr14:30627151
|
A | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-1058A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627151 | ||||||
| chr14:30627179
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.62-1030A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627179 | ||||||
| chr14:30627418
|
C | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.62-791C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627418 | ||||||
| chr14:30627468
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-741C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627468 | ||||||
| chr14:30627484
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.62-725C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627484 | ||||||
| chr14:30627485
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.62-724G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627485 | ||||||
| chr14:30627586
|
G | A | 11 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0034others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-623G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627586 | ||||||
| chr14:30627605
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.62-604G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627605 | ||||||
| chr14:30627658
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-551G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627658 | ||||||
| chr14:30627672
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.62-537G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627672 | ||||||
| chr14:30627699
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-510C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627699 | ||||||
| chr14:30627730
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-479C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627730 | ||||||
| chr14:30627745
|
GA | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.62-442delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30627745 | |||||
| chr14:30627745
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.62-452_62-442delAA others(9): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30627745 | |||||
| chr14:30627760
|
A | G | 77 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(74): Show | 77 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.62-449A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627760 | ||||||
| chr14:30627764
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 159 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.62-445A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30627764 | ||||||
| chr14:30627856
|
T | TA | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(10): Show | 13 | HG01243.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-335dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30627856 | |||||
| chr14:30627856
|
TA | T | 20 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0114others(17): Show | 20 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-335delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 30627856 | |||||
| chr14:30628037
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.62-172G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628037 | ||||||
| chr14:30628051
|
A | G | 4 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0305others(1): Show | 4 | HG00642.hp1 HG01496.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-158A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628051 | ||||||
| chr14:30628090
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-119G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628090 | ||||||
| chr14:30628094
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.62-115A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628094 | ||||||
| chr14:30628139
|
G | A | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.62-70G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628139 | ||||||
| chr14:30628188
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.62-21G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 1/24 | chr14 | 30628188 | ||||||
| chr14:30628332
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.132+53G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628332 | ||||||
| chr14:30628391
|
A | G | 1 | a0002c0002t0001g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.132+112A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628391 | ||||||
| chr14:30628547
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.132+268T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628547 | ||||||
| chr14:30628588
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.132+309A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628588 | ||||||
| chr14:30628598
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(6): Show | 9 | HG01891.hp1 HG01993.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+319G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628598 | ||||||
| chr14:30628725
|
A | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+446A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30628725 | ||||||
| chr14:30629220
|
G | T | 2 | a0001c0001t0001g0022a0001c0011t0001g0036 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.132+941G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629220 | ||||||
| chr14:30629319
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | NA19001.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.132+1040A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629319 | ||||||
| chr14:30629492
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133-985C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629492 | ||||||
| chr14:30629533
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.133-944T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629533 | ||||||
| chr14:30629533
|
TGTATTTG others(24): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.133-943_133-913del others(31): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629533 | ||||||
| chr14:30629565
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.133-912T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629565 | ||||||
| chr14:30629567
|
T | C | 1 | a0002c0002t0001g0222 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.133-910T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629567 | ||||||
| chr14:30629577
|
A | AT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG01074.hp2 HG01884.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.133-881dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 30629577 | |||||
| chr14:30629577
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-900A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629577 | ||||||
| chr14:30629577
|
AT | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-881delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 30629577 | |||||
| chr14:30629639
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.133-838G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629639 | ||||||
| chr14:30629641
|
A | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.133-836A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629641 | ||||||
| chr14:30629788
|
G | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.133-689G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629788 | ||||||
| chr14:30629819
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133-658G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629819 | ||||||
| chr14:30629934
|
AT | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.133-537delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 30629934 | |||||
| chr14:30629970
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.133-507G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30629970 | ||||||
| chr14:30630048
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.133-429C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30630048 | ||||||
| chr14:30630101
|
CTA | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-374_133-373del others(2): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 30630101 | |||||
| chr14:30630397
|
A | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.133-80A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 2/24 | chr14 | 30630397 | ||||||
| chr14:30630654
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+89T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30630654 | ||||||
| chr14:30630888
|
A | G | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(123): Show | 126 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.221+323A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30630888 | ||||||
| chr14:30630955
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.221+390C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30630955 | ||||||
| chr14:30631054
|
T | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+489T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631054 | ||||||
| chr14:30631229
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.221+664C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631229 | ||||||
| chr14:30631277
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.221+712C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631277 | ||||||
| chr14:30631282
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.221+717G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631282 | ||||||
| chr14:30631360
|
A | T | 1 | a0002c0002t0001g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.221+795A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631360 | ||||||
| chr14:30631467
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.221+902A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631467 | ||||||
| chr14:30631479
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 215 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.221+914T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631479 | ||||||
| chr14:30631514
|
A | G | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.221+949A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631514 | ||||||
| chr14:30631565
|
A | T | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(29): Show | 32 | HG01243.hp1 HG01243.hp2 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.221+1000A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631565 | ||||||
| chr14:30631794
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.221+1229C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631794 | ||||||
| chr14:30631812
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.221+1247C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30631812 | ||||||
| chr14:30632046
|
GAA | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0152a0002c0002t0001g0019others(7): Show | 10 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+1505_221+1506d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 30632046 | |||||
| chr14:30632046
|
GAAA | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 78 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.221+1504_221+1506d others(5): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 30632046 | |||||
| chr14:30632046
|
GAAAA | G | 122 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(119): Show | 122 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.221+1503_221+1506d others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 30632046 | |||||
| chr14:30632047
|
A | G | 1 | a0002c0003t0001g0313 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.221+1482A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632047 | ||||||
| chr14:30632051
|
A | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0052others(4): Show | 7 | HG02015.hp2 NA18612.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1486A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632051 | ||||||
| chr14:30632052
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.221+1487A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632052 | ||||||
| chr14:30632137
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.221+1572A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632137 | ||||||
| chr14:30632167
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.221+1602T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632167 | ||||||
| chr14:30632474
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.222-1473G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632474 | ||||||
| chr14:30632690
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.222-1257G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30632690 | ||||||
| chr14:30633223
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.222-724T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633223 | ||||||
| chr14:30633314
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.222-633G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633314 | ||||||
| chr14:30633370
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.222-577T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633370 | ||||||
| chr14:30633538
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.222-409G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633538 | ||||||
| chr14:30633599
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.222-348C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633599 | ||||||
| chr14:30633673
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-274A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633673 | ||||||
| chr14:30633782
|
TAAC | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-160_222-158del others(3): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 30633782 | |||||
| chr14:30633806
|
A | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.222-141A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633806 | ||||||
| chr14:30633810
|
G | A | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG01106.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-137G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 3/24 | chr14 | 30633810 | ||||||
| chr14:30634134
|
C | G | 1 | a0002c0002t0001g0295 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.312+97C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634134 | ||||||
| chr14:30634142
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.312+105T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634142 | ||||||
| chr14:30634219
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.312+182G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634219 | ||||||
| chr14:30634228
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 207 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.312+191A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634228 | ||||||
| chr14:30634329
|
A | G | 82 | a0002c0002t0001g0217a0002c0002t0001g0220a0002c0002t0001g0221others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.312+292A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634329 | ||||||
| chr14:30634432
|
G | A | 1 | a0002c0002t0001g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.312+395G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634432 | ||||||
| chr14:30634469
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.312+432A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634469 | ||||||
| chr14:30634501
|
T | C | 1 | a0002c0002t0001g0295 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.312+464T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634501 | ||||||
| chr14:30634584
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.312+547T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634584 | ||||||
| chr14:30634665
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.312+628G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634665 | ||||||
| chr14:30634685
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.312+648A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634685 | ||||||
| chr14:30634984
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.312+947T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634984 | ||||||
| chr14:30634994
|
T | C | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312+957T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30634994 | ||||||
| chr14:30635128
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.312+1091T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635128 | ||||||
| chr14:30635173
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+1136G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635173 | ||||||
| chr14:30635175
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.312+1138G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635175 | ||||||
| chr14:30635577
|
C | G | 1 | a0002c0002t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.312+1540C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635577 | ||||||
| chr14:30635635
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.312+1598G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635635 | ||||||
| chr14:30635635
|
G | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.312+1598G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635635 | ||||||
| chr14:30635691
|
G | A | 1 | a0002c0002t0001g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.312+1654G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635691 | ||||||
| chr14:30635749
|
C | G | 1 | a0002c0002t0001g0293 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.312+1712C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635749 | ||||||
| chr14:30635757
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.312+1720T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635757 | ||||||
| chr14:30635840
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.312+1803G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30635840 | ||||||
| chr14:30636145
|
G | A | 4 | a0002c0002t0001g0218a0002c0002t0001g0227a0002c0002t0001g0296others(1): Show | 4 | HG00642.hp2 HG02004.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-1980G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636145 | ||||||
| chr14:30636264
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.313-1861C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636264 | ||||||
| chr14:30636485
|
A | G | 2 | a0002c0002t0001g0246a0002c0002t0001g0309 | 2 | NA18947.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.313-1640A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636485 | ||||||
| chr14:30636588
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.313-1537T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636588 | ||||||
| chr14:30636638
|
G | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.313-1487G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636638 | ||||||
| chr14:30636872
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG00558.hp1 HG00673.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.313-1253G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30636872 | ||||||
| chr14:30637187
|
A | G | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(123): Show | 126 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.313-938A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30637187 | ||||||
| chr14:30637580
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.313-545A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30637580 | ||||||
| chr14:30638010
|
G | T | 1 | a0002c0002t0001g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313-115G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 4/24 | chr14 | 30638010 | ||||||
| chr14:30638311
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(27): Show | 31 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.435+64C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638311 | ||||||
| chr14:30638358
|
T | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.435+111T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638358 | ||||||
| chr14:30638371
|
A | G | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.435+124A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638371 | ||||||
| chr14:30638563
|
A | G | 1 | a0002c0002t0001g0305 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.435+316A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638563 | ||||||
| chr14:30638677
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.435+430A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638677 | ||||||
| chr14:30638710
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.435+463A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638710 | ||||||
| chr14:30638802
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.435+555A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638802 | ||||||
| chr14:30638874
|
C | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+627C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30638874 | ||||||
| chr14:30639397
|
C | A | 14 | a0002c0002t0001g0222a0002c0002t0001g0223a0002c0002t0001g0249others(11): Show | 14 | HG03927.hp1 NA18946.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.436-380C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30639397 | ||||||
| chr14:30639771
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(142): Show |
splice_region_variant&intron_variant | LOW | c.436-6T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 5/24 | chr14 | 30639771 | ||||||
| chr14:30640009
|
A | C | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+145A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640009 | ||||||
| chr14:30640069
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.523+205T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640069 | ||||||
| chr14:30640379
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+515C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640379 | ||||||
| chr14:30640383
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 39 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.523+519T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640383 | ||||||
| chr14:30640397
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.523+533A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640397 | ||||||
| chr14:30640664
|
A | C | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.523+800A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640664 | ||||||
| chr14:30640668
|
T | A | 1 | a0001c0006t0001g0073 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.523+804T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640668 | ||||||
| chr14:30640683
|
G | GT | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.523+828dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 30640683 | |||||
| chr14:30640983
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.523+1119G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30640983 | ||||||
| chr14:30641099
|
A | AG | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+1236dupG | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 30641099 | |||||
| chr14:30641282
|
A | G | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1418A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30641282 | ||||||
| chr14:30641789
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.524-1527A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30641789 | ||||||
| chr14:30641794
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.524-1522G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30641794 | ||||||
| chr14:30641820
|
A | C | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG03927.hp1 NA18965.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.524-1496A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30641820 | ||||||
| chr14:30642006
|
T | G | 99 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(96): Show | 99 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.524-1310T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642006 | ||||||
| chr14:30642136
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.524-1180G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642136 | ||||||
| chr14:30642170
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18965.hp2 NA18967.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-1146C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642170 | ||||||
| chr14:30642280
|
G | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-1036G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642280 | ||||||
| chr14:30642339
|
C | T | 1 | a0002c0002t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.524-977C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642339 | ||||||
| chr14:30642513
|
A | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0101a0001c0001t0001g0103others(2): Show | 5 | HG01496.hp1 HG02083.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-803A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642513 | ||||||
| chr14:30642654
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 38 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.524-662G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642654 | ||||||
| chr14:30642757
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.524-559C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642757 | ||||||
| chr14:30642891
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | NA19057.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.524-425G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30642891 | ||||||
| chr14:30643033
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.524-283C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30643033 | ||||||
| chr14:30643121
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.524-195C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 6/24 | chr14 | 30643121 | ||||||
| chr14:30643444
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+39A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643444 | ||||||
| chr14:30643513
|
A | G | 11 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0034others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+108A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643513 | ||||||
| chr14:30643612
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+207T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643612 | ||||||
| chr14:30643623
|
G | A | 82 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(79): Show | 82 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.613+218G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643623 | ||||||
| chr14:30643721
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.613+316G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643721 | ||||||
| chr14:30643830
|
A | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.613+425A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30643830 | ||||||
| chr14:30644029
|
A | G | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.613+624A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644029 | ||||||
| chr14:30644042
|
T | A | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.613+637T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644042 | ||||||
| chr14:30644104
|
G | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.613+699G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644104 | ||||||
| chr14:30644196
|
C | T | 1 | a0002c0002t0001g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.613+791C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644196 | ||||||
| chr14:30644209
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0151others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+804A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644209 | ||||||
| chr14:30644384
|
C | T | 1 | a0002c0002t0001g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.613+979C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644384 | ||||||
| chr14:30644461
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.613+1056T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644461 | ||||||
| chr14:30644500
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+1095C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644500 | ||||||
| chr14:30644758
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.613+1353C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644758 | ||||||
| chr14:30644759
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+1354G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644759 | ||||||
| chr14:30644842
|
G | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(40): Show | 44 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(41): Show |
intron_variant | MODIFIER | c.613+1437G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644842 | ||||||
| chr14:30644876
|
T | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1471T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644876 | ||||||
| chr14:30644902
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.613+1497C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644902 | ||||||
| chr14:30644991
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.613+1586T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30644991 | ||||||
| chr14:30645046
|
G | A | 1 | a0002c0002t0001g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.613+1641G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645046 | ||||||
| chr14:30645120
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.613+1715T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645120 | ||||||
| chr14:30645203
|
G | C | 1 | a0002c0002t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.613+1798G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645203 | ||||||
| chr14:30645282
|
T | C | 1 | a0002c0002t0001g0224 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.613+1877T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645282 | ||||||
| chr14:30645345
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.613+1940A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645345 | ||||||
| chr14:30645376
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.613+1971G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645376 | ||||||
| chr14:30645440
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.613+2035A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645440 | ||||||
| chr14:30645504
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG01106.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+2099C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645504 | ||||||
| chr14:30645588
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.613+2183A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645588 | ||||||
| chr14:30645644
|
T | G | 1 | a0002c0002t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.613+2239T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645644 | ||||||
| chr14:30645780
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.613+2375G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645780 | ||||||
| chr14:30645811
|
T | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.613+2406T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645811 | ||||||
| chr14:30645846
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+2441C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645846 | ||||||
| chr14:30645912
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613+2507C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30645912 | ||||||
| chr14:30646129
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.613+2724A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646129 | ||||||
| chr14:30646235
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.613+2830A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646235 | ||||||
| chr14:30646312
|
C | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+2907C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646312 | ||||||
| chr14:30646401
|
T | TTTTAGTT others(328): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0033 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.613+3009_613+3010i others(337): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 30646401 | |||||
| chr14:30646401
|
T | TTTTAGTT others(335): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.613+3009_613+3010i others(344): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 30646401 | |||||
| chr14:30646401
|
T | TTTTAGTT others(342): Show |
1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.613+3009_613+3010i others(351): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 30646401 | |||||
| chr14:30646637
|
A | G | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.614-2891A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646637 | ||||||
| chr14:30646640
|
A | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-2888A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646640 | ||||||
| chr14:30646642
|
A | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.614-2886A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646642 | ||||||
| chr14:30646762
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.614-2766G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646762 | ||||||
| chr14:30646806
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.614-2722T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646806 | ||||||
| chr14:30646848
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(40): Show | 44 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(41): Show |
intron_variant | MODIFIER | c.614-2680T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646848 | ||||||
| chr14:30646924
|
C | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.614-2604C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30646924 | ||||||
| chr14:30647108
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.614-2420C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647108 | ||||||
| chr14:30647152
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.614-2376A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647152 | ||||||
| chr14:30647227
|
A | G | 1 | a0002c0002t0001g0312 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.614-2301A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647227 | ||||||
| chr14:30647692
|
C | G | 1 | a0002c0002t0001g0257 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.614-1836C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647692 | ||||||
| chr14:30647887
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.614-1641G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647887 | ||||||
| chr14:30647898
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.614-1630G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647898 | ||||||
| chr14:30647932
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp2 HG01993.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-1596T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647932 | ||||||
| chr14:30647975
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.614-1553A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647975 | ||||||
| chr14:30647980
|
A | G | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.614-1548A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30647980 | ||||||
| chr14:30648183
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.614-1345C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648183 | ||||||
| chr14:30648349
|
A | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 46 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.614-1179A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648349 | ||||||
| chr14:30648540
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.614-988G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648540 | ||||||
| chr14:30648542
|
A | G | 125 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(122): Show | 125 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.614-986A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648542 | ||||||
| chr14:30648610
|
T | G | 1 | a0002c0002t0001g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.614-918T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648610 | ||||||
| chr14:30648773
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.614-755A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648773 | ||||||
| chr14:30648836
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.614-692T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648836 | ||||||
| chr14:30648855
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.614-673T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30648855 | ||||||
| chr14:30648975
|
C | CA | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 163 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.614-537dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 30648975 | |||||
| chr14:30649062
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.614-466T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649062 | ||||||
| chr14:30649088
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.614-440A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649088 | ||||||
| chr14:30649131
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.614-397G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649131 | ||||||
| chr14:30649148
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.614-380A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649148 | ||||||
| chr14:30649270
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.614-258C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649270 | ||||||
| chr14:30649344
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.614-184C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | chr14 | 30649344 | ||||||
| chr14:30649430
|
G | GT | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-97dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 30649430 | |||||
| chr14:30649761
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 192 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.669+178T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30649761 | ||||||
| chr14:30649793
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+210G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30649793 | ||||||
| chr14:30649812
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.669+229A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30649812 | ||||||
| chr14:30650050
|
A | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+467A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30650050 | ||||||
| chr14:30650154
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | NA18967.hp2 NA18982.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.670-411C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30650154 | ||||||
| chr14:30650218
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(27): Show | 31 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.670-347C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30650218 | ||||||
| chr14:30650271
|
AGT | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.670-290_670-289del others(2): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr14 | 30650271 | |||||
| chr14:30650353
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.670-212C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30650353 | ||||||
| chr14:30650528
|
A | C | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-37A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 8/24 | chr14 | 30650528 | ||||||
| chr14:30650657
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.755+7C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30650657 | ||||||
| chr14:30650945
|
T | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+295T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30650945 | ||||||
| chr14:30650990
|
A | G | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | NA18942.hp2 NA18954.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+340A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30650990 | ||||||
| chr14:30651197
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.755+547C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651197 | ||||||
| chr14:30651299
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.755+649G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651299 | ||||||
| chr14:30651425
|
C | CT | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.755+776dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr14 | 30651425 | |||||
| chr14:30651567
|
C | CT | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.755+930dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr14 | 30651567 | |||||
| chr14:30651605
|
TCTTA | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.755+960_755+963del others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr14 | 30651605 | |||||
| chr14:30651615
|
T | C | 1 | a0002c0002t0001g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.755+965T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651615 | ||||||
| chr14:30651638
|
G | T | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.755+988G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651638 | ||||||
| chr14:30651742
|
G | C | 1 | a0002c0002t0001g0225 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.755+1092G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651742 | ||||||
| chr14:30651827
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.755+1177G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651827 | ||||||
| chr14:30651851
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.755+1201G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651851 | ||||||
| chr14:30651906
|
A | G | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+1256A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651906 | ||||||
| chr14:30651909
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+1259T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651909 | ||||||
| chr14:30651959
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.755+1309T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30651959 | ||||||
| chr14:30652116
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.756-1373C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30652116 | ||||||
| chr14:30652245
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-1244T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30652245 | ||||||
| chr14:30652655
|
T | C | 1 | a0002c0002t0001g0298 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.756-834T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30652655 | ||||||
| chr14:30652718
|
G | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 40 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.756-771G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30652718 | ||||||
| chr14:30652834
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0012t0001g0210 | 3 | HG02886.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.756-655C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30652834 | ||||||
| chr14:30653004
|
A | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.756-485A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30653004 | ||||||
| chr14:30653027
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.756-462A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30653027 | ||||||
| chr14:30653127
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.756-362G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 9/24 | chr14 | 30653127 | ||||||
| chr14:30653616
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.855+28C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30653616 | ||||||
| chr14:30653737
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.855+149A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30653737 | ||||||
| chr14:30653869
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.855+281T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30653869 | ||||||
| chr14:30653894
|
C | T | 12 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0020others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.855+306C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30653894 | ||||||
| chr14:30653980
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.855+392G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30653980 | ||||||
| chr14:30653982
|
TA | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+404delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30653982 | |||||
| chr14:30654131
|
G | C | 33 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0108others(30): Show | 33 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.855+543G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654131 | ||||||
| chr14:30654140
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+552C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654140 | ||||||
| chr14:30654141
|
G | A | 124 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(121): Show | 124 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.855+553G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654141 | ||||||
| chr14:30654495
|
G | A | 1 | a0002c0002t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.855+907G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654495 | ||||||
| chr14:30654551
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.855+963G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654551 | ||||||
| chr14:30654572
|
GCTGAGGC others(55): Show |
G | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.855+988_855+1049de others(63): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30654572 | |||||
| chr14:30654641
|
T | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+1053T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654641 | ||||||
| chr14:30654673
|
C | CA | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 58 | HG01081.hp2 HG01106.hp2 HG01928.hp2 others(55): Show |
intron_variant | MODIFIER | c.855+1101dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30654673 | |||||
| chr14:30654694
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 40 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.855+1106A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654694 | ||||||
| chr14:30654811
|
A | G | 1 | a0002c0002t0001g0223 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.855+1223A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654811 | ||||||
| chr14:30654945
|
G | A | 14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG01074.hp1 HG01099.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.855+1357G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30654945 | ||||||
| chr14:30655259
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.855+1671A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655259 | ||||||
| chr14:30655296
|
T | C | 2 | a0002c0002t0001g0247a0002c0002t0001g0263 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.855+1708T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655296 | ||||||
| chr14:30655322
|
A | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+1734A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655322 | ||||||
| chr14:30655403
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+1815G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655403 | ||||||
| chr14:30655429
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.855+1841T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655429 | ||||||
| chr14:30655497
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.855+1909T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655497 | ||||||
| chr14:30655538
|
G | T | 77 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0040others(74): Show | 77 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.855+1950G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30655538 | ||||||
| chr14:30656046
|
T | C | 1 | a0002c0002t0001g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.855+2458T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30656046 | ||||||
| chr14:30656539
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.855+2951T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30656539 | ||||||
| chr14:30656545
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG01106.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+2957C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30656545 | ||||||
| chr14:30657074
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.855+3486A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657074 | ||||||
| chr14:30657211
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(127): Show | 130 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.855+3623G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657211 | ||||||
| chr14:30657223
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+3635A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657223 | ||||||
| chr14:30657442
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.855+3854G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657442 | ||||||
| chr14:30657473
|
T | A | 1 | a0002c0002t0001g0306 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.855+3885T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657473 | ||||||
| chr14:30657516
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+3928G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657516 | ||||||
| chr14:30657532
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.855+3944T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657532 | ||||||
| chr14:30657653
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.855+4065T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657653 | ||||||
| chr14:30657719
|
A | G | 1 | a0002c0002t0001g0292 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.855+4131A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657719 | ||||||
| chr14:30657961
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.855+4373A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30657961 | ||||||
| chr14:30658000
|
T | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 47 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.855+4412T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658000 | ||||||
| chr14:30658134
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.855+4546G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658134 | ||||||
| chr14:30658190
|
G | C | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.855+4602G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658190 | ||||||
| chr14:30658378
|
T | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+4790T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658378 | ||||||
| chr14:30658445
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.855+4857T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658445 | ||||||
| chr14:30658887
|
C | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.855+5299C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658887 | ||||||
| chr14:30658911
|
G | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(27): Show | 31 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.855+5323G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658911 | ||||||
| chr14:30658967
|
T | C | 75 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.855+5379T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30658967 | ||||||
| chr14:30659040
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.855+5452C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659040 | ||||||
| chr14:30659139
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.855+5551T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659139 | ||||||
| chr14:30659173
|
G | GT | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0099others(12): Show | 15 | HG01261.hp1 HG01496.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.855+5602dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30659173 | |||||
| chr14:30659173
|
GT | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.855+5602delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30659173 | |||||
| chr14:30659257
|
A | G | 75 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(72): Show | 75 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.855+5669A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659257 | ||||||
| chr14:30659342
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.855+5754G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659342 | ||||||
| chr14:30659353
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.855+5765A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659353 | ||||||
| chr14:30659440
|
T | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+5852T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659440 | ||||||
| chr14:30659445
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.855+5857G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659445 | ||||||
| chr14:30659602
|
G | A | 1 | a0002c0002t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.855+6014G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659602 | ||||||
| chr14:30659622
|
TAAACAGC others(13): Show |
T | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.855+6038_855+6057d others(22): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30659622 | |||||
| chr14:30659767
|
AT | A | 76 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(73): Show | 76 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.855+6188delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30659767 | |||||
| chr14:30659796
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.855+6208G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30659796 | ||||||
| chr14:30659982
|
AATACTTC others(7): Show |
A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+6397_855+6410d others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30659982 | |||||
| chr14:30660023
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.855+6435C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660023 | ||||||
| chr14:30660067
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0012t0001g0210 | 3 | HG02886.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.855+6479T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660067 | ||||||
| chr14:30660235
|
A | G | 1 | a0002c0002t0001g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.855+6647A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660235 | ||||||
| chr14:30660275
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.855+6687T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660275 | ||||||
| chr14:30660287
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0197others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+6699G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660287 | ||||||
| chr14:30660302
|
CTAAT | C | 3 | a0002c0002t0001g0241a0002c0002t0001g0246a0002c0002t0001g0309 | 3 | NA18947.hp2 NA18993.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.855+6716_855+6719d others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30660302 | |||||
| chr14:30660327
|
A | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 36 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.855+6739A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660327 | ||||||
| chr14:30660336
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.855+6748A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660336 | ||||||
| chr14:30660370
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+6782T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660370 | ||||||
| chr14:30660509
|
G | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.855+6921G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660509 | ||||||
| chr14:30660555
|
A | G | 1 | a0002c0002t0001g0291 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.855+6967A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660555 | ||||||
| chr14:30660591
|
C | G | 1 | a0002c0002t0001g0291 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.855+7003C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660591 | ||||||
| chr14:30660744
|
T | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+7156T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660744 | ||||||
| chr14:30660844
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+7256A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30660844 | ||||||
| chr14:30661014
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.855+7426A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661014 | ||||||
| chr14:30661128
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.855+7540A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661128 | ||||||
| chr14:30661184
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 47 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.855+7596A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661184 | ||||||
| chr14:30661201
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.855+7613A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661201 | ||||||
| chr14:30661305
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.855+7717A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661305 | ||||||
| chr14:30661560
|
G | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.855+7972G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661560 | ||||||
| chr14:30661628
|
G | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 47 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.855+8040G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661628 | ||||||
| chr14:30661799
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.855+8211G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30661799 | ||||||
| chr14:30662209
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-8047C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30662209 | ||||||
| chr14:30662505
|
CTT | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-7750_856-7749d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30662505 | ||||||
| chr14:30662802
|
C | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-7454C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30662802 | ||||||
| chr14:30662938
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.856-7318G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30662938 | ||||||
| chr14:30663039
|
T | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-7217T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663039 | ||||||
| chr14:30663042
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.856-7214T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663042 | ||||||
| chr14:30663195
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-7061A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663195 | ||||||
| chr14:30663425
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.856-6831G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663425 | ||||||
| chr14:30663483
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.856-6773C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663483 | ||||||
| chr14:30663539
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.856-6717T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663539 | ||||||
| chr14:30663953
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.856-6303T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30663953 | ||||||
| chr14:30664150
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.856-6106C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664150 | ||||||
| chr14:30664236
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(6): Show | 9 | HG01243.hp2 HG01358.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-6020C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664236 | ||||||
| chr14:30664261
|
G | A | 11 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0034others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.856-5995G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664261 | ||||||
| chr14:30664388
|
C | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.856-5868C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664388 | ||||||
| chr14:30664483
|
G | A | 6 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-5773G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664483 | ||||||
| chr14:30664544
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.856-5712A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664544 | ||||||
| chr14:30664588
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-5668A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664588 | ||||||
| chr14:30664723
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-5533A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664723 | ||||||
| chr14:30664729
|
C | T | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-5527C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664729 | ||||||
| chr14:30664742
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.856-5514A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664742 | ||||||
| chr14:30664788
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 219 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.856-5468A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664788 | ||||||
| chr14:30664810
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.856-5446A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664810 | ||||||
| chr14:30664858
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.856-5398A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30664858 | ||||||
| chr14:30665056
|
A | G | 1 | a0002c0002t0001g0290 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.856-5200A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665056 | ||||||
| chr14:30665056
|
A | T | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.856-5200A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665056 | ||||||
| chr14:30665096
|
T | C | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.856-5160T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665096 | ||||||
| chr14:30665104
|
G | C | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-5152G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665104 | ||||||
| chr14:30665116
|
G | GA | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-5134dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30665116 | |||||
| chr14:30665169
|
G | C | 2 | a0002c0002t0001g0223a0002c0002t0001g0251 | 2 | NA18946.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.856-5087G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665169 | ||||||
| chr14:30665230
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.856-5026G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665230 | ||||||
| chr14:30665281
|
A | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-4975A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665281 | ||||||
| chr14:30665303
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.856-4953G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665303 | ||||||
| chr14:30665358
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.856-4898T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665358 | ||||||
| chr14:30665456
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.856-4800C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665456 | ||||||
| chr14:30665508
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 219 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.856-4748T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665508 | ||||||
| chr14:30665651
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 56 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.856-4605A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665651 | ||||||
| chr14:30665761
|
GACTTTAA | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-4492_856-4486d others(9): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30665761 | |||||
| chr14:30665788
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.856-4468G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665788 | ||||||
| chr14:30665973
|
T | A | 1 | a0002c0002t0001g0318 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.856-4283T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30665973 | ||||||
| chr14:30666315
|
T | A | 2 | a0002c0002t0001g0247a0002c0002t0001g0263 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-3941T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666315 | ||||||
| chr14:30666408
|
G | A | 1 | a0002c0002t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.856-3848G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666408 | ||||||
| chr14:30666527
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.856-3729G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666527 | ||||||
| chr14:30666677
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.856-3579A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666677 | ||||||
| chr14:30666695
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.856-3561C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666695 | ||||||
| chr14:30666696
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 39 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.856-3560G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666696 | ||||||
| chr14:30666736
|
C | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-3520C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666736 | ||||||
| chr14:30666769
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.856-3487A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666769 | ||||||
| chr14:30666842
|
A | G | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-3414A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666842 | ||||||
| chr14:30666902
|
A | G | 1 | a0002c0002t0001g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.856-3354A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666902 | ||||||
| chr14:30666931
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-3325A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666931 | ||||||
| chr14:30666933
|
A | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp2 HG01993.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-3323A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30666933 | ||||||
| chr14:30667215
|
G | T | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.856-3041G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667215 | ||||||
| chr14:30667582
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.856-2674A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667582 | ||||||
| chr14:30667733
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-2523A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667733 | ||||||
| chr14:30667865
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.856-2391A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667865 | ||||||
| chr14:30667880
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.856-2376C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667880 | ||||||
| chr14:30667886
|
C | T | 129 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(126): Show | 129 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.856-2370C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667886 | ||||||
| chr14:30667888
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.856-2368C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667888 | ||||||
| chr14:30667906
|
C | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp2 HG01993.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-2350C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667906 | ||||||
| chr14:30667968
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.856-2288C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667968 | ||||||
| chr14:30667991
|
A | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-2265A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30667991 | ||||||
| chr14:30668015
|
C | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-2241C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668015 | ||||||
| chr14:30668028
|
T | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(127): Show | 130 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.856-2228T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668028 | ||||||
| chr14:30668059
|
A | G | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-2197A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668059 | ||||||
| chr14:30668166
|
A | AACCAAAA others(15): Show |
1 | a0001c0001t0001g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.856-2088_856-2087i others(24): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30668166 | |||||
| chr14:30668169
|
G | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.856-2087G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668169 | ||||||
| chr14:30668340
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.856-1916A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668340 | ||||||
| chr14:30668452
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.856-1804G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668452 | ||||||
| chr14:30668565
|
A | G | 1 | a0002c0002t0001g0243 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.856-1691A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668565 | ||||||
| chr14:30668627
|
A | T | 1 | a0002c0002t0001g0232 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.856-1629A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668627 | ||||||
| chr14:30668782
|
C | G | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-1474C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668782 | ||||||
| chr14:30668871
|
A | G | 11 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0034others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.856-1385A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668871 | ||||||
| chr14:30668943
|
A | G | 1 | a0001c0012t0001g0210 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856-1313A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668943 | ||||||
| chr14:30668952
|
G | T | 1 | a0002c0002t0001g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.856-1304G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668952 | ||||||
| chr14:30668953
|
G | T | 1 | a0002c0002t0001g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.856-1303G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30668953 | ||||||
| chr14:30669013
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.856-1243A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669013 | ||||||
| chr14:30669018
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | NA18612.hp1 NA19067.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.856-1238A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669018 | ||||||
| chr14:30669172
|
G | A | 21 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0074others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.856-1084G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669172 | ||||||
| chr14:30669422
|
C | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-834C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669422 | ||||||
| chr14:30669478
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.856-778T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669478 | ||||||
| chr14:30669516
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.856-740T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669516 | ||||||
| chr14:30669544
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.856-712G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669544 | ||||||
| chr14:30669553
|
G | GT | 41 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 42 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(39): Show |
intron_variant | MODIFIER | c.856-695dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30669553 | |||||
| chr14:30669561
|
T | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-695T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669561 | ||||||
| chr14:30669628
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0192 | 2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.856-628C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30669628 | ||||||
| chr14:30669965
|
AAAATT | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-288_856-284del others(5): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 30669965 | |||||
| chr14:30670003
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-253A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670003 | ||||||
| chr14:30670022
|
C | T | 7 | a0002c0002t0001g0230a0002c0002t0001g0231a0002c0002t0001g0232others(4): Show | 7 | HG00558.hp2 HG02027.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-234C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670022 | ||||||
| chr14:30670088
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.856-168A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670088 | ||||||
| chr14:30670129
|
G | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00323.hp1 HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.856-127G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670129 | ||||||
| chr14:30670143
|
G | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.856-113G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670143 | ||||||
| chr14:30670162
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.856-94T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670162 | ||||||
| chr14:30670191
|
C | A | 3 | a0003c0004t0002g0148a0003c0005t0002g0146a0003c0005t0002g0147 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.856-65C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 10/24 | chr14 | 30670191 | ||||||
| chr14:30670559
|
T | G | 2 | a0002c0002t0001g0205a0002c0002t0001g0207 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.995+164T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670559 | ||||||
| chr14:30670665
|
C | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 46 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.995+270C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670665 | ||||||
| chr14:30670677
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.995+282A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670677 | ||||||
| chr14:30670714
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.995+319C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670714 | ||||||
| chr14:30670728
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.995+333G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670728 | ||||||
| chr14:30670771
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.995+376C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670771 | ||||||
| chr14:30670797
|
G | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.995+402G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670797 | ||||||
| chr14:30670874
|
A | G | 1 | a0002c0002t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.995+479A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670874 | ||||||
| chr14:30670996
|
C | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 216 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.995+601C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30670996 | ||||||
| chr14:30671848
|
A | G | 1 | a0002c0002t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.996-1409A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30671848 | ||||||
| chr14:30672014
|
T | TA | 41 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(38): Show | 41 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.996-1229dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 30672014 | |||||
| chr14:30672014
|
T | TAA | 11 | a0001c0001t0001g0118a0001c0001t0001g0143a0001c0001t0001g0160others(8): Show | 11 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.996-1230_996-1229d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 30672014 | |||||
| chr14:30672028
|
A | G | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.996-1229A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672028 | ||||||
| chr14:30672028
|
AG | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0097others(5): Show | 8 | HG00558.hp1 HG01168.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.996-1228delG | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672028 | ||||||
| chr14:30672029
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(205): Show |
intron_variant | MODIFIER | c.996-1228G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672029 | ||||||
| chr14:30672318
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.996-939A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672318 | ||||||
| chr14:30672493
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.996-764T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672493 | ||||||
| chr14:30672527
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.996-730G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672527 | ||||||
| chr14:30672538
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.996-719A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672538 | ||||||
| chr14:30672857
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.996-400C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672857 | ||||||
| chr14:30672869
|
C | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.996-388C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672869 | ||||||
| chr14:30672956
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.996-301T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672956 | ||||||
| chr14:30672972
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.996-285G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30672972 | ||||||
| chr14:30673049
|
A | C | 1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.996-208A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30673049 | ||||||
| chr14:30673211
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.996-46G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 11/24 | chr14 | 30673211 | ||||||
| chr14:30673417
|
G | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1086+70G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673417 | ||||||
| chr14:30673436
|
T | A | 1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1086+89T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673436 | ||||||
| chr14:30673633
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1086+286G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673633 | ||||||
| chr14:30673637
|
A | C | 1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087-287A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673637 | ||||||
| chr14:30673647
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1087-277G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673647 | ||||||
| chr14:30673659
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1087-265G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673659 | ||||||
| chr14:30673726
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1087-198C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673726 | ||||||
| chr14:30673734
|
A | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1087-190A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673734 | ||||||
| chr14:30673750
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1087-174A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673750 | ||||||
| chr14:30673859
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1087-65G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 12/24 | chr14 | 30673859 | ||||||
| chr14:30674007
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1160+10C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674007 | ||||||
| chr14:30674052
|
T | A | 2 | a0002c0002t0001g0233a0002c0002t0001g0267 | 2 | HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1160+55T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674052 | ||||||
| chr14:30674139
|
G | A | 1 | a0002c0002t0001g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1160+142G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674139 | ||||||
| chr14:30674172
|
C | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1160+175C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674172 | ||||||
| chr14:30674185
|
A | C | 1 | a0002c0002t0001g0226 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1160+188A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674185 | ||||||
| chr14:30674230
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1160+233T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674230 | ||||||
| chr14:30674273
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1160+276C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674273 | ||||||
| chr14:30674336
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1160+339T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674336 | ||||||
| chr14:30674368
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160+371C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674368 | ||||||
| chr14:30674413
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1160+416C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674413 | ||||||
| chr14:30674425
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1160+428A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674425 | ||||||
| chr14:30674551
|
G | T | 1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1161-433G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674551 | ||||||
| chr14:30674643
|
C | CA | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 47 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1161-333dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr14 | 30674643 | |||||
| chr14:30674689
|
C | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 47 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1161-295C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 13/24 | chr14 | 30674689 | ||||||
| chr14:30675544
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1242+479G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30675544 | ||||||
| chr14:30675640
|
CTAT | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0197others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1242+580_1242+582d others(5): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30675640 | |||||
| chr14:30675751
|
T | G | 1 | a0002c0002t0001g0269 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1242+686T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30675751 | ||||||
| chr14:30675849
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1242+784A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30675849 | ||||||
| chr14:30675985
|
C | T | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1242+920C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30675985 | ||||||
| chr14:30676522
|
G | A | 1 | a0002c0002t0001g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1242+1457G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30676522 | ||||||
| chr14:30676531
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+1466G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30676531 | ||||||
| chr14:30676893
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1242+1828C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30676893 | ||||||
| chr14:30677030
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1242+1965A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677030 | ||||||
| chr14:30677077
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1242+2012G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677077 | ||||||
| chr14:30677336
|
A | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.1242+2271A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677336 | ||||||
| chr14:30677398
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1242+2333G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677398 | ||||||
| chr14:30677488
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(56): Show | 60 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(57): Show |
intron_variant | MODIFIER | c.1242+2423A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677488 | ||||||
| chr14:30677572
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1242+2507G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677572 | ||||||
| chr14:30677618
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1242+2553C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677618 | ||||||
| chr14:30677623
|
T | TTTC | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 147 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1242+2561_1242+256 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677623 | |||||
| chr14:30677699
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1242+2634G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677699 | ||||||
| chr14:30677709
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA19067.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1242+2644G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677709 | ||||||
| chr14:30677716
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1242+2651G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677716 | ||||||
| chr14:30677800
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1242+2735C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677800 | ||||||
| chr14:30677827
|
C | CT | 118 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(115): Show | 118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1242+2793dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
C | CTT | 40 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0041others(37): Show | 41 | HG00673.hp2 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1242+2792_1242+279 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
C | CTTT | 10 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242+2791_1242+279 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1242+2774_1242+279 others(24): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
CT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1242+2793delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1242+2781_1242+279 others(17): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677827
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1242+2780_1242+279 others(18): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30677827 | |||||
| chr14:30677893
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1242+2828G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677893 | ||||||
| chr14:30677901
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+2836A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677901 | ||||||
| chr14:30677989
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1242+2924A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30677989 | ||||||
| chr14:30678050
|
G | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0034others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242+2985G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678050 | ||||||
| chr14:30678058
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1242+2993A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678058 | ||||||
| chr14:30678120
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1242+3055G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678120 | ||||||
| chr14:30678129
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1242+3064C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678129 | ||||||
| chr14:30678212
|
A | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 39 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.1242+3147A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678212 | ||||||
| chr14:30678271
|
G | A | 6 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0202others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1242+3206G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678271 | ||||||
| chr14:30678292
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 207 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.1242+3227C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678292 | ||||||
| chr14:30678324
|
T | A | 1 | a0002c0002t0001g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1242+3259T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678324 | ||||||
| chr14:30678370
|
T | A | 1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1242+3305T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678370 | ||||||
| chr14:30678388
|
T | C | 32 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0095others(29): Show | 32 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1242+3323T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678388 | ||||||
| chr14:30678435
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1242+3370A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678435 | ||||||
| chr14:30678611
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02015.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1242+3546T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678611 | ||||||
| chr14:30678617
|
A | G | 1 | a0002c0002t0001g0250 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1242+3552A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678617 | ||||||
| chr14:30678671
|
GC | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1242+3608delC | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30678671 | |||||
| chr14:30678898
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1242+3833T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678898 | ||||||
| chr14:30678907
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0115 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1242+3842T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678907 | ||||||
| chr14:30678980
|
C | A | 15 | a0001c0001t0001g0025a0001c0001t0001g0151a0001c0001t0001g0152others(12): Show | 15 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1242+3915C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30678980 | ||||||
| chr14:30679065
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242+4000C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679065 | ||||||
| chr14:30679228
|
A | AT | 35 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0061others(32): Show | 35 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1242+4176dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30679228 | |||||
| chr14:30679228
|
AT | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01243.hp2 HG01358.hp2 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1242+4176delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30679228 | |||||
| chr14:30679509
|
T | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1242+4444T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679509 | ||||||
| chr14:30679679
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1242+4614C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679679 | ||||||
| chr14:30679683
|
CT | C | 130 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0032others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1242+4633delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30679683 | |||||
| chr14:30679683
|
CTT | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0151others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1242+4632_1242+463 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30679683 | |||||
| chr14:30679745
|
A | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0151others(14): Show | 17 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1242+4680A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679745 | ||||||
| chr14:30679820
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1242+4755C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679820 | ||||||
| chr14:30679855
|
A | C | 2 | a0002c0002t0001g0220a0002c0002t0001g0289 | 2 | HG00544.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.1242+4790A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679855 | ||||||
| chr14:30679858
|
A | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+4793A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679858 | ||||||
| chr14:30679873
|
C | G | 86 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(83): Show | 86 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1242+4808C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679873 | ||||||
| chr14:30679970
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1242+4905A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30679970 | ||||||
| chr14:30680077
|
T | G | 2 | a0002c0002t0001g0226a0002c0002t0001g0308 | 2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1242+5012T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680077 | ||||||
| chr14:30680144
|
C | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1242+5079C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680144 | ||||||
| chr14:30680398
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1242+5333A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680398 | ||||||
| chr14:30680424
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242+5359A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680424 | ||||||
| chr14:30680550
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0011 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1242+5485A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680550 | ||||||
| chr14:30680705
|
A | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242+5640A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680705 | ||||||
| chr14:30680960
|
C | T | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1242+5895C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680960 | ||||||
| chr14:30680987
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242+5922C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30680987 | ||||||
| chr14:30681096
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1242+6031G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681096 | ||||||
| chr14:30681214
|
C | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+6149C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681214 | ||||||
| chr14:30681220
|
C | CA | 122 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(119): Show | 122 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1242+6170dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681220 | |||||
| chr14:30681220
|
C | CAA | 6 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0111others(3): Show | 6 | HG01175.hp1 HG02055.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1242+6169_1242+617 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681220 | |||||
| chr14:30681350
|
C | T | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1242+6285C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681350 | ||||||
| chr14:30681489
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1242+6424A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681489 | ||||||
| chr14:30681521
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+6456A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681521 | ||||||
| chr14:30681602
|
G | GCTCAATA others(6130): Show |
1 | a0002c0002t0001g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6141): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6130): Show |
1 | a0002c0002t0001g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6141): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6095): Show |
1 | a0002c0002t0001g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6106): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6095): Show |
1 | a0002c0003t0001g0313 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6106): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6095): Show |
1 | a0002c0002t0001g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6106): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6096): Show |
1 | a0002c0002t0001g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6107): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6096): Show |
7 | a0002c0002t0001g0310a0002c0002t0001g0311a0002c0002t0001g0318others(4): Show | 7 | HG00733.hp2 HG01081.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1242+6555_1242+655 others(6107): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6097): Show |
1 | a0002c0002t0001g0321 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6108): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6097): Show |
1 | a0002c0002t0001g0257 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6108): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6097): Show |
1 | a0002c0002t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6108): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6098): Show |
1 | a0002c0002t0001g0289 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6109): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
1 | a0002c0002t0001g0269 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
2 | a0002c0002t0001g0253a0002c0002t0001g0254 | 2 | NA18990.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6129): Show |
1 | a0002c0002t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6140): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6103): Show |
1 | a0002c0002t0001g0260 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6114): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6129): Show |
2 | a0001c0001t0001g0216a0002c0002t0001g0251 | 2 | NA18946.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1242+6555_1242+655 others(6140): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6129): Show |
1 | a0002c0002t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6140): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6129): Show |
1 | a0002c0002t0001g0223 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6140): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6130): Show |
1 | a0002c0002t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6141): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6130): Show |
1 | a0002c0002t0001g0224 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6141): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
1 | a0002c0002t0001g0301 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
2 | a0002c0002t0001g0222a0002c0002t0001g0249 | 2 | NA18983.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
1 | a0002c0002t0001g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6131): Show |
1 | a0002c0002t0001g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6142): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6132): Show |
1 | a0002c0002t0001g0256 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6143): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6132): Show |
1 | a0002c0002t0001g0225 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6143): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6132): Show |
1 | a0002c0002t0001g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6143): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6133): Show |
1 | a0004c0007t0001g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6144): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6132): Show |
1 | a0002c0002t0001g0258 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6143): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6132): Show |
1 | a0002c0002t0001g0259 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6143): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681602
|
G | GCTCAATA others(6133): Show |
1 | a0002c0002t0001g0250 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1242+6555_1242+655 others(6144): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30681602 | |||||
| chr14:30681613
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1242+6548A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681613 | ||||||
| chr14:30681614
|
T | C | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1242+6549T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681614 | ||||||
| chr14:30681651
|
C | A | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1242+6586C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30681651 | ||||||
| chr14:30682018
|
T | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+6953T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682018 | ||||||
| chr14:30682106
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1242+7041A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682106 | ||||||
| chr14:30682117
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1242+7052G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682117 | ||||||
| chr14:30682192
|
A | G | 1 | a0002c0002t0001g0321 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1242+7127A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682192 | ||||||
| chr14:30682243
|
T | C | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(123): Show | 126 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1242+7178T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682243 | ||||||
| chr14:30682542
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1242+7477G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682542 | ||||||
| chr14:30682560
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1242+7495A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682560 | ||||||
| chr14:30682741
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242+7676A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30682741 | ||||||
| chr14:30683016
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 154 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1242+7951C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683016 | ||||||
| chr14:30683037
|
A | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242+7972A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683037 | ||||||
| chr14:30683305
|
A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242+8240A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683305 | ||||||
| chr14:30683371
|
A | G | 1 | a0001c0010t0001g0051 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1242+8306A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683371 | ||||||
| chr14:30683467
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1242+8402T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683467 | ||||||
| chr14:30683529
|
A | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+8464A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683529 | ||||||
| chr14:30683620
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1242+8555A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683620 | ||||||
| chr14:30683924
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1242+8859G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683924 | ||||||
| chr14:30683984
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 159 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1242+8919G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683984 | ||||||
| chr14:30683993
|
A | G | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.1242+8928A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30683993 | ||||||
| chr14:30684078
|
A | G | 1 | a0002c0002t0001g0224 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1242+9013A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684078 | ||||||
| chr14:30684117
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(40): Show | 44 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(41): Show |
intron_variant | MODIFIER | c.1242+9052C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684117 | ||||||
| chr14:30684160
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1242+9095G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684160 | ||||||
| chr14:30684213
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1242+9148G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684213 | ||||||
| chr14:30684223
|
C | T | 2 | a0002c0002t0001g0226a0002c0002t0001g0308 | 2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1242+9158C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684223 | ||||||
| chr14:30684276
|
G | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+9211G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684276 | ||||||
| chr14:30684462
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242+9397G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684462 | ||||||
| chr14:30684474
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1242+9409T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684474 | ||||||
| chr14:30684547
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1242+9482G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684547 | ||||||
| chr14:30684559
|
G | A | 1 | a0002c0002t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1242+9494G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684559 | ||||||
| chr14:30684586
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1242+9521T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684586 | ||||||
| chr14:30684728
|
C | CT | 41 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0030others(38): Show | 42 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1242+9682dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684728 | |||||
| chr14:30684728
|
CT | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1242+9682delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684728 | |||||
| chr14:30684803
|
C | CT | 9 | a0001c0001t0001g0168a0002c0002t0001g0020a0002c0002t0001g0202others(6): Show | 9 | HG01169.hp2 HG01884.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1242+9757dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684803 | |||||
| chr14:30684803
|
C | CTT | 45 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0030others(42): Show | 46 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1242+9756_1242+975 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684803 | |||||
| chr14:30684803
|
C | CTTT | 52 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(49): Show | 52 | HG00558.hp1 HG00733.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1242+9755_1242+975 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684803 | |||||
| chr14:30684803
|
C | CTTTT | 95 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 95 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1242+9754_1242+975 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684803 | |||||
| chr14:30684803
|
C | CTTTTT | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(14): Show | 17 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1242+9753_1242+975 others(9): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30684803 | |||||
| chr14:30684967
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-9806A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684967 | ||||||
| chr14:30684970
|
C | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-9803C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30684970 | ||||||
| chr14:30685033
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1243-9740T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685033 | ||||||
| chr14:30685036
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1243-9737C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685036 | ||||||
| chr14:30685079
|
C | T | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1243-9694C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685079 | ||||||
| chr14:30685081
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1243-9692A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685081 | ||||||
| chr14:30685203
|
A | T | 15 | a0001c0001t0001g0216a0002c0002t0001g0222a0002c0002t0001g0223others(12): Show | 15 | HG03927.hp1 NA18946.hp1 NA18953.hp2 others(12): Show |
intron_variant | MODIFIER | c.1243-9570A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685203 | ||||||
| chr14:30685259
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1243-9514C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685259 | ||||||
| chr14:30685411
|
C | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1243-9362C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685411 | ||||||
| chr14:30685454
|
A | G | 1 | a0002c0002t0001g0224 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1243-9319A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685454 | ||||||
| chr14:30685458
|
C | T | 1 | a0002c0002t0001g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1243-9315C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685458 | ||||||
| chr14:30685518
|
T | C | 1 | a0002c0002t0001g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1243-9255T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685518 | ||||||
| chr14:30685528
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1243-9245T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685528 | ||||||
| chr14:30685638
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-9135G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685638 | ||||||
| chr14:30685736
|
G | A | 2 | a0001c0001t0001g0091a0002c0002t0001g0245 | 2 | HG01261.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1243-9037G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685736 | ||||||
| chr14:30685757
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1243-9016A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685757 | ||||||
| chr14:30685762
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1243-9011G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685762 | ||||||
| chr14:30685808
|
G | T | 1 | a0002c0002t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1243-8965G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685808 | ||||||
| chr14:30685816
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1243-8957T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685816 | ||||||
| chr14:30685855
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-8918C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685855 | ||||||
| chr14:30685945
|
G | A | 1 | a0002c0002t0001g0312 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1243-8828G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685945 | ||||||
| chr14:30685952
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1243-8821G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30685952 | ||||||
| chr14:30686004
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-8769G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686004 | ||||||
| chr14:30686062
|
T | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1243-8711T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686062 | ||||||
| chr14:30686070
|
T | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1243-8703T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686070 | ||||||
| chr14:30686078
|
C | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(27): Show | 31 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.1243-8695C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686078 | ||||||
| chr14:30686130
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1243-8643A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686130 | ||||||
| chr14:30686219
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1243-8554G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686219 | ||||||
| chr14:30686243
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1243-8530T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686243 | ||||||
| chr14:30686270
|
T | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1243-8503T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686270 | ||||||
| chr14:30686293
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1243-8480G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686293 | ||||||
| chr14:30686460
|
C | A | 2 | a0002c0002t0001g0244a0002c0002t0001g0326 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1243-8313C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686460 | ||||||
| chr14:30686569
|
A | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-8204A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686569 | ||||||
| chr14:30686593
|
C | T | 21 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0074others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1243-8180C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686593 | ||||||
| chr14:30686596
|
T | C | 1 | a0002c0002t0001g0299 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1243-8177T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686596 | ||||||
| chr14:30686702
|
G | C | 1 | a0002c0002t0001g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1243-8071G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686702 | ||||||
| chr14:30686717
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1243-8056G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686717 | ||||||
| chr14:30686719
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1243-8054C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686719 | ||||||
| chr14:30686720
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0159 | 3 | HG02257.hp2 HG02735.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1243-8053G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686720 | ||||||
| chr14:30686750
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0186 | 2 | NA18978.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1243-8023G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686750 | ||||||
| chr14:30686847
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0001g0123 | 3 | NA18968.hp1 NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1243-7926A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686847 | ||||||
| chr14:30686870
|
A | T | 1 | a0002c0002t0001g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1243-7903A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686870 | ||||||
| chr14:30686873
|
G | A | 1 | a0002c0002t0001g0265 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1243-7900G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686873 | ||||||
| chr14:30686881
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1243-7892G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686881 | ||||||
| chr14:30686891
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1243-7882A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30686891 | ||||||
| chr14:30687024
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1243-7749G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687024 | ||||||
| chr14:30687116
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1243-7657T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687116 | ||||||
| chr14:30687127
|
G | A | 3 | a0001c0001t0001g0039a0003c0004t0002g0149a0003c0004t0002g0150 | 3 | HG02647.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1243-7646G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687127 | ||||||
| chr14:30687150
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1243-7623C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687150 | ||||||
| chr14:30687208
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-7565G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687208 | ||||||
| chr14:30687272
|
C | T | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1243-7501C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687272 | ||||||
| chr14:30687281
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1243-7492G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687281 | ||||||
| chr14:30687464
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG00673.hp2 HG02129.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-7309A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687464 | ||||||
| chr14:30687490
|
A | C | 1 | a0002c0002t0001g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1243-7283A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687490 | ||||||
| chr14:30687491
|
G | T | 1 | a0002c0002t0001g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1243-7282G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687491 | ||||||
| chr14:30687547
|
T | A | 2 | a0002c0002t0001g0233a0002c0002t0001g0267 | 2 | HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1243-7226T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687547 | ||||||
| chr14:30687548
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1243-7225G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687548 | ||||||
| chr14:30687650
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1243-7123A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687650 | ||||||
| chr14:30687807
|
A | G | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243-6966A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30687807 | ||||||
| chr14:30688025
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1243-6748G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688025 | ||||||
| chr14:30688053
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243-6720G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688053 | ||||||
| chr14:30688120
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1243-6653G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688120 | ||||||
| chr14:30688216
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-6557G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688216 | ||||||
| chr14:30688232
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1243-6541A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688232 | ||||||
| chr14:30688234
|
C | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0145others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1243-6539C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688234 | ||||||
| chr14:30688384
|
T | C | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-6389T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688384 | ||||||
| chr14:30688514
|
A | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0197others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-6259A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688514 | ||||||
| chr14:30688522
|
G | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0197others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-6251G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688522 | ||||||
| chr14:30688523
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0197others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-6250G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688523 | ||||||
| chr14:30688582
|
C | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1243-6191C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688582 | ||||||
| chr14:30688603
|
T | TA | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(52): Show | 56 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.1243-6168dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30688603 | |||||
| chr14:30688610
|
G | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-6163G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688610 | ||||||
| chr14:30688615
|
A | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(10): Show | 13 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243-6158A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688615 | ||||||
| chr14:30688619
|
G | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-6154G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688619 | ||||||
| chr14:30688648
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1243-6125T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688648 | ||||||
| chr14:30688715
|
G | A | 140 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(137): Show | 140 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.1243-6058G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688715 | ||||||
| chr14:30688766
|
C | T | 125 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(122): Show | 125 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1243-6007C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688766 | ||||||
| chr14:30688857
|
G | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1243-5916G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688857 | ||||||
| chr14:30688894
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1243-5879A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688894 | ||||||
| chr14:30688907
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1243-5866C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688907 | ||||||
| chr14:30688928
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1243-5845G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688928 | ||||||
| chr14:30688930
|
A | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-5843A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688930 | ||||||
| chr14:30688943
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02145.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243-5830G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688943 | ||||||
| chr14:30688952
|
C | T | 2 | a0001c0001t0001g0022a0001c0011t0001g0036 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1243-5821C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688952 | ||||||
| chr14:30688953
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1243-5820G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30688953 | ||||||
| chr14:30689094
|
A | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-5679A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689094 | ||||||
| chr14:30689116
|
T | G | 1 | a0002c0002t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1243-5657T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689116 | ||||||
| chr14:30689203
|
C | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-5570C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689203 | ||||||
| chr14:30689239
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1243-5534C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689239 | ||||||
| chr14:30689297
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18954.hp2 NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1243-5476G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689297 | ||||||
| chr14:30689309
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-5464G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689309 | ||||||
| chr14:30689336
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1243-5437A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689336 | ||||||
| chr14:30689461
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1243-5312T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689461 | ||||||
| chr14:30689540
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1243-5233C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689540 | ||||||
| chr14:30689642
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-5131C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689642 | ||||||
| chr14:30689693
|
G | T | 1 | a0003c0005t0002g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1243-5080G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689693 | ||||||
| chr14:30689790
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1243-4983G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689790 | ||||||
| chr14:30689798
|
C | CCTT | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-4972_1243-497 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30689798 | |||||
| chr14:30689862
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1243-4911G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689862 | ||||||
| chr14:30689869
|
TGGA | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-4896_1243-489 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30689869 | |||||
| chr14:30689891
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1243-4882G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689891 | ||||||
| chr14:30689915
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1243-4858T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689915 | ||||||
| chr14:30689953
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1243-4820T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30689953 | ||||||
| chr14:30690016
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1243-4757T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690016 | ||||||
| chr14:30690069
|
C | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-4704C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690069 | ||||||
| chr14:30690069
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1243-4704C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690069 | ||||||
| chr14:30690070
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1243-4703G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690070 | ||||||
| chr14:30690151
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0141others(3): Show | 6 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243-4622G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690151 | ||||||
| chr14:30690165
|
C | G | 7 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0141others(4): Show | 7 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-4608C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690165 | ||||||
| chr14:30690207
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0191 | 2 | HG01891.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1243-4566T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690207 | ||||||
| chr14:30690218
|
G | A | 41 | a0001c0001t0001g0191a0002c0002t0001g0220a0002c0002t0001g0226others(38): Show | 41 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1243-4555G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690218 | ||||||
| chr14:30690232
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1243-4541C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690232 | ||||||
| chr14:30690354
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0066others(10): Show | 13 | HG00544.hp1 HG00735.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243-4419T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690354 | ||||||
| chr14:30690393
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1243-4380G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690393 | ||||||
| chr14:30690405
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG01106.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243-4368C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690405 | ||||||
| chr14:30690414
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.1243-4359C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690414 | ||||||
| chr14:30690418
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-4355C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690418 | ||||||
| chr14:30690420
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1243-4353C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690420 | ||||||
| chr14:30690436
|
C | CA | 4 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0069others(1): Show | 4 | HG02155.hp1 NA18971.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243-4336dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30690436 | |||||
| chr14:30690441
|
T | C | 1 | a0002c0002t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1243-4332T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690441 | ||||||
| chr14:30690524
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1243-4249C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690524 | ||||||
| chr14:30690547
|
A | G | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1243-4226A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690547 | ||||||
| chr14:30690559
|
A | G | 3 | a0001c0001t0001g0042a0002c0002t0001g0034a0002c0002t0001g0035 | 3 | HG01243.hp1 HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-4214A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690559 | ||||||
| chr14:30690597
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1243-4176T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690597 | ||||||
| chr14:30690666
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 154 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1243-4107G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690666 | ||||||
| chr14:30690668
|
C | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-4105C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690668 | ||||||
| chr14:30690684
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1243-4089A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690684 | ||||||
| chr14:30690708
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 40 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.1243-4065T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690708 | ||||||
| chr14:30690714
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0087a0003c0004t0002g0148others(4): Show | 7 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1243-4059G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690714 | ||||||
| chr14:30690735
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-4038G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690735 | ||||||
| chr14:30690740
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1243-4033T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690740 | ||||||
| chr14:30690777
|
C | G | 2 | a0002c0002t0001g0236a0002c0002t0001g0268 | 2 | HG01070.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1243-3996C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690777 | ||||||
| chr14:30690800
|
C | T | 2 | a0002c0002t0001g0246a0002c0002t0001g0309 | 2 | NA18947.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1243-3973C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690800 | ||||||
| chr14:30690817
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1243-3956G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30690817 | ||||||
| chr14:30691011
|
G | A | 2 | a0002c0002t0001g0242a0002c0002t0001g0243 | 2 | NA19012.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1243-3762G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691011 | ||||||
| chr14:30691251
|
T | C | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1243-3522T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691251 | ||||||
| chr14:30691491
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1243-3282A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691491 | ||||||
| chr14:30691586
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1243-3187C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691586 | ||||||
| chr14:30691773
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243-3000A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691773 | ||||||
| chr14:30691839
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-2934C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691839 | ||||||
| chr14:30691932
|
C | CTTTA | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1243-2807_1243-280 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
C | CTTTATTT others(1): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 108 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.1243-2811_1243-280 others(12): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
C | CTTTATTT others(5): Show |
34 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0061others(31): Show | 34 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1243-2815_1243-280 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
C | CTTTATTT others(9): Show |
4 | a0001c0001t0001g0028a0001c0001t0001g0121a0001c0001t0001g0136others(1): Show | 4 | HG00544.hp2 HG00741.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243-2819_1243-280 others(20): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
CTTTA | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0215a0002c0002t0001g0019 | 3 | HG02523.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1243-2807_1243-280 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
CTTTATTT others(1): Show |
C | 9 | a0002c0002t0001g0020a0002c0002t0001g0201a0002c0002t0001g0202others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1243-2811_1243-280 others(12): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691932
|
CTTTATTT others(5): Show |
C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG00639.hp2 HG00735.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1243-2815_1243-280 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 30691932 | |||||
| chr14:30691982
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-2791A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30691982 | ||||||
| chr14:30692056
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-2717G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692056 | ||||||
| chr14:30692086
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1243-2687A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692086 | ||||||
| chr14:30692129
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1243-2644A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692129 | ||||||
| chr14:30692185
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1243-2588A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692185 | ||||||
| chr14:30692211
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1243-2562A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692211 | ||||||
| chr14:30692365
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1243-2408T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692365 | ||||||
| chr14:30692720
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1243-2053G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692720 | ||||||
| chr14:30692957
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1243-1816C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30692957 | ||||||
| chr14:30693123
|
G | T | 1 | a0002c0002t0001g0309 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1243-1650G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693123 | ||||||
| chr14:30693138
|
A | G | 1 | a0002c0002t0001g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1243-1635A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693138 | ||||||
| chr14:30693244
|
G | A | 1 | a0001c0010t0001g0051 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1243-1529G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693244 | ||||||
| chr14:30693499
|
G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1243-1274G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693499 | ||||||
| chr14:30693854
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(28): Show | 32 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1243-919T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693854 | ||||||
| chr14:30693972
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-801G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30693972 | ||||||
| chr14:30694161
|
T | G | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1243-612T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694161 | ||||||
| chr14:30694207
|
T | A | 76 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(73): Show | 76 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1243-566T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694207 | ||||||
| chr14:30694207
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1243-566T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694207 | ||||||
| chr14:30694309
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1243-464T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694309 | ||||||
| chr14:30694339
|
T | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1243-434T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694339 | ||||||
| chr14:30694669
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18965.hp2 NA18967.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243-104A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694669 | ||||||
| chr14:30694708
|
G | A | 1 | a0002c0002t0001g0241 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1243-65G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 14/24 | chr14 | 30694708 | ||||||
| chr14:30694914
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339+45G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30694914 | ||||||
| chr14:30695102
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1339+233T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695102 | ||||||
| chr14:30695138
|
A | G | 5 | a0002c0002t0001g0310a0002c0002t0001g0311a0002c0002t0001g0314others(2): Show | 5 | HG01081.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339+269A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695138 | ||||||
| chr14:30695231
|
A | G | 1 | a0002c0002t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1339+362A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695231 | ||||||
| chr14:30695242
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1339+373A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695242 | ||||||
| chr14:30695243
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1339+374G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695243 | ||||||
| chr14:30695244
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1339+375A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695244 | ||||||
| chr14:30695413
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1339+544C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695413 | ||||||
| chr14:30695707
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1339+838C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695707 | ||||||
| chr14:30695760
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1339+891T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695760 | ||||||
| chr14:30695970
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0066others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339+1101C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695970 | ||||||
| chr14:30695985
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1339+1116T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30695985 | ||||||
| chr14:30696073
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0062others(32): Show | 35 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1339+1204G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696073 | ||||||
| chr14:30696399
|
A | C | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1339+1530A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696399 | ||||||
| chr14:30696425
|
A | T | 1 | a0002c0002t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1339+1556A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696425 | ||||||
| chr14:30696460
|
GATTTATC others(9): Show |
G | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1339+1597_1339+161 others(20): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr14 | 30696460 | |||||
| chr14:30696587
|
C | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1339+1718C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696587 | ||||||
| chr14:30696607
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339+1738A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696607 | ||||||
| chr14:30696626
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1339+1757G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696626 | ||||||
| chr14:30696754
|
G | A | 1 | a0002c0002t0001g0280 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1339+1885G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696754 | ||||||
| chr14:30696826
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1339+1957A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30696826 | ||||||
| chr14:30697045
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1339+2176G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697045 | ||||||
| chr14:30697074
|
G | T | 1 | a0002c0002t0001g0312 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1339+2205G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697074 | ||||||
| chr14:30697516
|
G | A | 2 | a0001c0001t0001g0072a0001c0010t0001g0051 | 2 | NA18944.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1339+2647G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697516 | ||||||
| chr14:30697529
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1340-2659G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697529 | ||||||
| chr14:30697529
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1340-2659G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697529 | ||||||
| chr14:30697735
|
T | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1340-2453T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30697735 | ||||||
| chr14:30698014
|
TA | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1340-2172delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr14 | 30698014 | |||||
| chr14:30698169
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1340-2019A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698169 | ||||||
| chr14:30698182
|
G | A | 32 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0095others(29): Show | 32 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1340-2006G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698182 | ||||||
| chr14:30698224
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1340-1964G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698224 | ||||||
| chr14:30698228
|
G | A | 124 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(121): Show | 124 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1340-1960G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698228 | ||||||
| chr14:30698434
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0011 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1340-1754T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698434 | ||||||
| chr14:30698666
|
TAGTTGCG others(15): Show |
T | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1340-1518_1340-149 others(26): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr14 | 30698666 | |||||
| chr14:30698862
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1340-1326A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698862 | ||||||
| chr14:30698907
|
G | A | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1340-1281G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30698907 | ||||||
| chr14:30699039
|
C | T | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1340-1149C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699039 | ||||||
| chr14:30699140
|
C | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(42): Show | 46 | HG01106.hp2 HG01358.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.1340-1048C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699140 | ||||||
| chr14:30699174
|
T | G | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1340-1014T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699174 | ||||||
| chr14:30699241
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1340-947G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699241 | ||||||
| chr14:30699303
|
A | G | 1 | a0002c0002t0001g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1340-885A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699303 | ||||||
| chr14:30699434
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0129 | 2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1340-754A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699434 | ||||||
| chr14:30699440
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1340-748C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699440 | ||||||
| chr14:30699728
|
G | A | 125 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(122): Show | 125 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1340-460G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699728 | ||||||
| chr14:30699861
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1340-327T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30699861 | ||||||
| chr14:30700058
|
G | A | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1340-130G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 15/24 | chr14 | 30700058 | ||||||
| chr14:30700366
|
T | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0095others(3): Show | 6 | NA18939.hp1 NA18941.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1410+108T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30700366 | ||||||
| chr14:30700472
|
G | A | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1410+214G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30700472 | ||||||
| chr14:30700525
|
T | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1410+267T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30700525 | ||||||
| chr14:30700661
|
A | C | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1410+403A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30700661 | ||||||
| chr14:30700799
|
T | C | 2 | a0002c0002t0001g0224a0002c0002t0001g0302 | 2 | HG00099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1410+541T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30700799 | ||||||
| chr14:30701001
|
G | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1410+743G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30701001 | ||||||
| chr14:30701591
|
C | CTATATAT | 4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG00558.hp1 HG00673.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-704_1411-698d others(9): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr14 | 30701591 | |||||
| chr14:30701606
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 220 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.1411-690T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30701606 | ||||||
| chr14:30701708
|
G | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411-588G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30701708 | ||||||
| chr14:30701958
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1411-338G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30701958 | ||||||
| chr14:30702027
|
A | G | 3 | a0002c0003t0001g0285a0002c0003t0001g0286a0002c0003t0001g0287 | 3 | NA18948.hp1 NA18959.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1411-269A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30702027 | ||||||
| chr14:30702036
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0212 | 2 | HG00673.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1411-260G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 16/24 | chr14 | 30702036 | ||||||
| chr14:30702521
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1490+146G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30702521 | ||||||
| chr14:30702624
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1490+249C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30702624 | ||||||
| chr14:30703042
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1490+667C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703042 | ||||||
| chr14:30703047
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.1490+672T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703047 | ||||||
| chr14:30703057
|
TA | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(10): Show | 13 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1490+696delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703057 | |||||
| chr14:30703376
|
C | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0115 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1490+1001C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703376 | ||||||
| chr14:30703558
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1490+1183A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703558 | ||||||
| chr14:30703638
|
CAAG | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1490+1265_1490+126 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703638 | |||||
| chr14:30703643
|
G | T | 4 | a0002c0002t0001g0218a0002c0002t0001g0227a0002c0002t0001g0296others(1): Show | 4 | HG00642.hp2 HG02004.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1490+1268G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703643 | ||||||
| chr14:30703910
|
C | CAT | 15 | a0001c0001t0001g0052a0001c0001t0001g0084a0002c0002t0001g0217others(12): Show | 15 | HG00323.hp1 HG00544.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1490+1587_1490+158 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
C | CATAT | 8 | a0002c0002t0001g0241a0002c0002t0001g0274a0002c0002t0001g0277others(5): Show | 8 | HG00323.hp2 HG00642.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490+1585_1490+158 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
C | CATATAT | 4 | a0002c0002t0001g0221a0002c0002t0001g0233a0002c0002t0001g0282others(1): Show | 4 | HG01070.hp2 HG03942.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1490+1583_1490+158 others(10): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
C | CATATATA others(1): Show |
5 | a0002c0002t0001g0219a0002c0002t0001g0246a0002c0002t0001g0297others(2): Show | 5 | HG02809.hp2 HG03710.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1490+1581_1490+158 others(12): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
C | CATATATA others(5): Show |
1 | a0002c0002t0001g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1490+1577_1490+158 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
C | CATATATA others(7): Show |
2 | a0002c0002t0001g0272a0002c0002t0001g0283 | 2 | HG02155.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1490+1575_1490+158 others(18): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CAT | C | 13 | a0001c0001t0001g0189a0002c0002t0001g0226a0002c0002t0001g0228others(10): Show | 13 | HG00099.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1490+1587_1490+158 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATAT | C | 11 | a0002c0002t0001g0224a0002c0002t0001g0234a0002c0002t0001g0238others(8): Show | 11 | HG00738.hp2 HG01106.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1490+1585_1490+158 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATAT | C | 4 | a0002c0002t0001g0239a0002c0002t0001g0269a0002c0002t0001g0270others(1): Show | 4 | HG00735.hp2 HG02083.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490+1583_1490+158 others(10): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(3): Show |
C | 2 | a0002c0002t0001g0225a0002c0002t0001g0311 | 2 | HG01975.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1490+1579_1490+158 others(14): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(5): Show |
C | 1 | a0002c0002t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1490+1577_1490+158 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(13): Show |
C | 2 | a0002c0002t0001g0227a0002c0002t0001g0267 | 2 | HG02004.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1490+1569_1490+158 others(24): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(19): Show |
C | 6 | a0002c0002t0001g0245a0002c0002t0001g0262a0002c0002t0001g0280others(3): Show | 6 | HG00741.hp2 HG01261.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1490+1563_1490+158 others(30): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(21): Show |
C | 17 | a0001c0001t0001g0216a0002c0002t0001g0222a0002c0002t0001g0223others(14): Show | 17 | HG03927.hp1 NA18946.hp1 NA18952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1490+1561_1490+158 others(32): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(23): Show |
C | 1 | a0002c0002t0001g0268 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1490+1559_1490+158 others(34): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(27): Show |
C | 3 | a0002c0002t0001g0230a0002c0002t0001g0231a0002c0002t0001g0232 | 3 | HG00558.hp2 HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1490+1555_1490+158 others(38): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(29): Show |
C | 1 | a0002c0002t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1490+1553_1490+158 others(40): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703910
|
CATATATA others(31): Show |
C | 1 | a0002c0002t0001g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1490+1551_1490+158 others(42): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703910 | |||||
| chr14:30703922
|
TATATATA others(35): Show |
T | 11 | a0001c0001t0001g0101a0001c0001t0001g0103a0002c0002t0001g0019others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1490+1551_1490+159 others(46): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703922 | |||||
| chr14:30703928
|
TATATATA others(29): Show |
T | 2 | a0001c0001t0001g0014a0001c0001t0001g0038 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1490+1557_1490+159 others(40): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703928 | |||||
| chr14:30703930
|
TATATATA others(27): Show |
T | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(11): Show | 14 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1490+1559_1490+159 others(38): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703930 | |||||
| chr14:30703934
|
TATATATA others(23): Show |
T | 4 | a0001c0001t0001g0171a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG02109.hp1 HG03669.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490+1563_1490+159 others(34): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703934 | |||||
| chr14:30703936
|
TATATATA others(21): Show |
T | 36 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(33): Show | 36 | HG00673.hp1 HG01168.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.1490+1565_1490+159 others(32): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703936 | |||||
| chr14:30703938
|
TATATATA others(19): Show |
T | 25 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(22): Show | 26 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1490+1567_1490+159 others(30): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703938 | |||||
| chr14:30703940
|
T | A | 1 | a0002c0002t0001g0309 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1490+1565T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703940 | ||||||
| chr14:30703940
|
TATATATA others(17): Show |
T | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 21 | HG00558.hp1 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1490+1569_1490+159 others(28): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703940 | |||||
| chr14:30703942
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0001g0153a0001c0001t0001g0200 | 2 | HG01243.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1490+1571_1490+159 others(26): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703942 | |||||
| chr14:30703944
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0193 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1490+1573_1490+159 others(24): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703944 | |||||
| chr14:30703946
|
TATATATA others(10): Show |
T | 1 | a0002c0002t0001g0312 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1490+1573_1490+158 others(21): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703946 | |||||
| chr14:30703946
|
TATATATA others(11): Show |
T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02015.hp1 HG02027.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1490+1575_1490+159 others(22): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703946 | |||||
| chr14:30703948
|
TATATATA others(9): Show |
T | 13 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0118others(10): Show | 13 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1490+1577_1490+159 others(20): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703948 | |||||
| chr14:30703950
|
TATATATA others(7): Show |
T | 8 | a0001c0001t0001g0132a0001c0001t0001g0163a0001c0001t0001g0211others(5): Show | 8 | HG01109.hp1 HG02129.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490+1579_1490+159 others(18): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703950 | |||||
| chr14:30703952
|
TATATATA others(5): Show |
T | 9 | a0001c0001t0001g0049a0001c0001t0001g0081a0001c0001t0001g0083others(6): Show | 9 | HG01175.hp1 HG01975.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1490+1581_1490+159 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703952 | |||||
| chr14:30703954
|
TATATATA others(3): Show |
T | 20 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0043others(17): Show | 20 | HG01074.hp2 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1490+1583_1490+159 others(14): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703954 | |||||
| chr14:30703956
|
TATATATA others(1): Show |
T | 13 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1490+1585_1490+159 others(12): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703956 | |||||
| chr14:30703958
|
TATATAA | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0053others(2): Show | 5 | HG01934.hp1 HG02148.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1490+1587_1490+159 others(10): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703958 | |||||
| chr14:30703960
|
TATAA | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0124others(6): Show | 9 | HG02293.hp2 HG02886.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1490+1590_1490+159 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703960 | |||||
| chr14:30703962
|
TAA | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG00733.hp1 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1490+1589_1490+159 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703962 | |||||
| chr14:30703964
|
A | T | 15 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0074others(12): Show | 15 | HG00323.hp1 HG01358.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1490+1589A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703964 | ||||||
| chr14:30703966
|
T | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1490+1591T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30703966 | ||||||
| chr14:30703966
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1490+1592_1490+159 others(16): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703966 | |||||
| chr14:30703966
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1490+1592_1490+159 others(20): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 30703966 | |||||
| chr14:30704028
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1490+1653C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704028 | ||||||
| chr14:30704238
|
C | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0171a0001c0001t0001g0172others(20): Show | 24 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.1491-1585C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704238 | ||||||
| chr14:30704335
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1491-1488A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704335 | ||||||
| chr14:30704455
|
A | G | 1 | a0002c0002t0001g0234 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1491-1368A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704455 | ||||||
| chr14:30704497
|
A | G | 1 | a0005c0009t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1491-1326A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704497 | ||||||
| chr14:30704498
|
G | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1491-1325G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704498 | ||||||
| chr14:30704511
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1491-1312G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704511 | ||||||
| chr14:30704707
|
C | G | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1491-1116C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704707 | ||||||
| chr14:30704860
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491-963G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704860 | ||||||
| chr14:30704887
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1491-936C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704887 | ||||||
| chr14:30704948
|
T | G | 6 | a0002c0002t0001g0238a0002c0002t0001g0318a0002c0002t0001g0320others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491-875T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30704948 | ||||||
| chr14:30705031
|
A | C | 1 | a0002c0002t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1491-792A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30705031 | ||||||
| chr14:30705345
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1491-478A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30705345 | ||||||
| chr14:30705401
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG00733.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1491-422A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 17/24 | chr14 | 30705401 | ||||||
| chr14:30705944
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1553+59A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30705944 | ||||||
| chr14:30706031
|
G | GT | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1553+156dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr14 | 30706031 | |||||
| chr14:30706367
|
G | A | 6 | a0002c0002t0001g0238a0002c0002t0001g0318a0002c0002t0001g0320others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1553+482G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706367 | ||||||
| chr14:30706541
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0136 | 2 | HG00741.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1553+656G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706541 | ||||||
| chr14:30706563
|
T | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1553+678T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706563 | ||||||
| chr14:30706669
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 45 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.1553+784A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706669 | ||||||
| chr14:30706790
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1553+905A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706790 | ||||||
| chr14:30706933
|
A | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1553+1048A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30706933 | ||||||
| chr14:30707291
|
C | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1554-699C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30707291 | ||||||
| chr14:30707403
|
T | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1554-587T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30707403 | ||||||
| chr14:30707442
|
T | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1554-548T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30707442 | ||||||
| chr14:30707682
|
CA | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1554-298delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr14 | 30707682 | |||||
| chr14:30707721
|
T | G | 1 | a0002c0002t0001g0283 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1554-269T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 18/24 | chr14 | 30707721 | ||||||
| chr14:30708257
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1629+192G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708257 | ||||||
| chr14:30708278
|
G | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(33): Show | 36 | HG01106.hp2 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.1629+213G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708278 | ||||||
| chr14:30708343
|
C | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(15): Show | 18 | HG00639.hp2 HG00735.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1629+278C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708343 | ||||||
| chr14:30708360
|
T | C | 2 | a0001c0001t0001g0022a0001c0011t0001g0036 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1629+295T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708360 | ||||||
| chr14:30708389
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1629+324T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708389 | ||||||
| chr14:30708491
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1629+426T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708491 | ||||||
| chr14:30708494
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1629+429A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708494 | ||||||
| chr14:30708530
|
TA | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 215 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.1629+474delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30708530 | |||||
| chr14:30708606
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1629+541C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708606 | ||||||
| chr14:30708624
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1629+559A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708624 | ||||||
| chr14:30708683
|
A | C | 1 | a0002c0002t0001g0310 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1629+618A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708683 | ||||||
| chr14:30708686
|
CAG | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.1629+625_1629+626d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30708686 | |||||
| chr14:30708746
|
CAA | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1629+684_1629+685d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30708746 | |||||
| chr14:30708821
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1629+756C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708821 | ||||||
| chr14:30708826
|
A | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1629+761A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708826 | ||||||
| chr14:30708833
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+768A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708833 | ||||||
| chr14:30708880
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.1629+815T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30708880 | ||||||
| chr14:30708935
|
ATTTG | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0091others(3): Show | 6 | NA18747.hp2 NA18948.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629+874_1629+877d others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30708935 | |||||
| chr14:30709011
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 214 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.1629+946G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709011 | ||||||
| chr14:30709130
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+1065T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709130 | ||||||
| chr14:30709381
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1629+1316C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709381 | ||||||
| chr14:30709472
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1629+1407A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709472 | ||||||
| chr14:30709507
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1629+1442C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709507 | ||||||
| chr14:30709712
|
A | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+1647A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709712 | ||||||
| chr14:30709747
|
C | T | 1 | a0002c0002t0001g0233 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1629+1682C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709747 | ||||||
| chr14:30709761
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1629+1696C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709761 | ||||||
| chr14:30709919
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1629+1854A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709919 | ||||||
| chr14:30709989
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1629+1924G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30709989 | ||||||
| chr14:30710023
|
G | T | 1 | a0002c0002t0001g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1629+1958G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710023 | ||||||
| chr14:30710073
|
C | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+2008C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710073 | ||||||
| chr14:30710166
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1629+2101A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710166 | ||||||
| chr14:30710332
|
T | TA | 122 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(119): Show | 123 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1629+2290dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710332 | |||||
| chr14:30710332
|
T | TAA | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG01169.hp1 HG01243.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.1629+2289_1629+229 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710332 | |||||
| chr14:30710332
|
TA | T | 11 | a0001c0001t0001g0099a0002c0002t0001g0034a0002c0002t0001g0035others(8): Show | 11 | HG01070.hp2 HG01243.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1629+2290delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710332 | |||||
| chr14:30710332
|
TAAA | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+2288_1629+229 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710332 | |||||
| chr14:30710332
|
TAAAAAA | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0052others(6): Show | 9 | HG02615.hp1 HG02965.hp2 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+2285_1629+229 others(10): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710332 | |||||
| chr14:30710388
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1629+2323G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710388 | ||||||
| chr14:30710395
|
A | G | 1 | a0002c0002t0001g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1629+2330A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710395 | ||||||
| chr14:30710416
|
T | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1629+2351T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710416 | ||||||
| chr14:30710450
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1629+2385A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710450 | ||||||
| chr14:30710457
|
C | CT | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629+2400dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30710457 | |||||
| chr14:30710606
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1629+2541C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710606 | ||||||
| chr14:30710614
|
A | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0091others(3): Show | 6 | NA18747.hp2 NA18948.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629+2549A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710614 | ||||||
| chr14:30710700
|
G | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1629+2635G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710700 | ||||||
| chr14:30710731
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1629+2666A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710731 | ||||||
| chr14:30710816
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1629+2751A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710816 | ||||||
| chr14:30710864
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+2799G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710864 | ||||||
| chr14:30710864
|
G | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629+2799G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30710864 | ||||||
| chr14:30711028
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1629+2963A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711028 | ||||||
| chr14:30711097
|
A | G | 1 | a0002c0002t0001g0310 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1629+3032A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711097 | ||||||
| chr14:30711153
|
ACT | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp2 HG01993.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+3093_1629+309 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30711153 | |||||
| chr14:30711325
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1629+3260A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711325 | ||||||
| chr14:30711351
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 38 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1629+3286T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711351 | ||||||
| chr14:30711476
|
T | C | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+3411T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711476 | ||||||
| chr14:30711498
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+3433T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711498 | ||||||
| chr14:30711514
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1629+3449C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711514 | ||||||
| chr14:30711627
|
T | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 38 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1629+3562T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711627 | ||||||
| chr14:30711660
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1629+3595G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711660 | ||||||
| chr14:30711682
|
C | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0153others(6): Show | 9 | HG01243.hp2 HG01993.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1629+3617C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711682 | ||||||
| chr14:30711692
|
T | C | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1629+3627T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711692 | ||||||
| chr14:30711941
|
G | A | 1 | a0002c0002t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1629+3876G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711941 | ||||||
| chr14:30711973
|
T | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1629+3908T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711973 | ||||||
| chr14:30711998
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1630-3926G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30711998 | ||||||
| chr14:30712058
|
T | TCTGGTTT others(309): Show |
1 | a0001c0001t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(320): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(312): Show |
1 | a0001c0001t0001g0174 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(323): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(313): Show |
1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(324): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(327): Show |
1 | a0001c0001t0001g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(338): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(328): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0182a0001c0001t0001g0184others(1): Show | 4 | NA18612.hp2 NA18942.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-3851_1630-385 others(339): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(329): Show |
13 | a0001c0001t0001g0026a0001c0001t0001g0122a0001c0001t0001g0125others(10): Show | 13 | HG02015.hp1 HG02027.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1630-3851_1630-385 others(340): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(330): Show |
12 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0119others(9): Show | 12 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1630-3851_1630-385 others(341): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(331): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0132 | 2 | HG03688.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1630-3851_1630-385 others(342): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(333): Show |
1 | a0001c0001t0001g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(344): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(334): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0215 | 2 | HG02523.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1630-3851_1630-385 others(345): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712058
|
T | TCTGGTTT others(335): Show |
1 | a0001c0001t0001g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1630-3851_1630-385 others(346): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30712058 | |||||
| chr14:30712159
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0094 | 3 | HG02155.hp1 NA18988.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1630-3765C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712159 | ||||||
| chr14:30712194
|
C | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-3730C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712194 | ||||||
| chr14:30712320
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630-3604A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712320 | ||||||
| chr14:30712463
|
C | A | 1 | a0002c0002t0001g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1630-3461C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712463 | ||||||
| chr14:30712480
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1630-3444A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712480 | ||||||
| chr14:30712618
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1630-3306T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712618 | ||||||
| chr14:30712685
|
C | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-3239C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712685 | ||||||
| chr14:30712933
|
A | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630-2991A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30712933 | ||||||
| chr14:30713044
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1630-2880C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30713044 | ||||||
| chr14:30713356
|
TAAAAACC others(30): Show |
T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1630-2530_1630-249 others(41): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30713356 | |||||
| chr14:30713466
|
A | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(21): Show | 25 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1630-2458A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30713466 | ||||||
| chr14:30713595
|
C | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18965.hp2 NA18967.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-2329C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30713595 | ||||||
| chr14:30713783
|
C | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.1630-2141C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30713783 | ||||||
| chr14:30713962
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.1630-1962A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30713962 | ||||||
| chr14:30714191
|
C | CA | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.1630-1720dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30714191 | |||||
| chr14:30714191
|
C | CAA | 12 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0209others(9): Show | 12 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1630-1721_1630-172 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30714191 | |||||
| chr14:30714217
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-1707A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714217 | ||||||
| chr14:30714356
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1630-1568G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714356 | ||||||
| chr14:30714360
|
C | CA | 9 | a0001c0001t0001g0109a0002c0002t0001g0019a0002c0002t0001g0020others(6): Show | 9 | HG02040.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1630-1548dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30714360 | |||||
| chr14:30714360
|
CA | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00323.hp1 HG00544.hp2 HG00673.hp2 others(142): Show |
intron_variant | MODIFIER | c.1630-1548delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30714360 | |||||
| chr14:30714383
|
A | AT | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-1537dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30714383 | |||||
| chr14:30714480
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1630-1444C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714480 | ||||||
| chr14:30714555
|
C | A | 1 | a0002c0002t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1630-1369C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714555 | ||||||
| chr14:30714703
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG00741.hp1 HG01074.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1630-1221A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714703 | ||||||
| chr14:30714736
|
T | G | 1 | a0002c0002t0001g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1630-1188T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714736 | ||||||
| chr14:30714840
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630-1084G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714840 | ||||||
| chr14:30714929
|
A | G | 14 | a0002c0002t0001g0222a0002c0002t0001g0223a0002c0002t0001g0249others(11): Show | 14 | HG03927.hp1 NA18946.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.1630-995A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30714929 | ||||||
| chr14:30715090
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1630-834T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30715090 | ||||||
| chr14:30715291
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1630-633G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30715291 | ||||||
| chr14:30715400
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1630-524G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30715400 | ||||||
| chr14:30715568
|
C | CA | 136 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 136 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1630-340dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30715568 | |||||
| chr14:30715568
|
C | CAA | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0063others(5): Show | 8 | HG00621.hp2 HG01975.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-341_1630-340d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30715568 | |||||
| chr14:30715763
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1630-161A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30715763 | ||||||
| chr14:30715778
|
A | C | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1630-146A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | chr14 | 30715778 | ||||||
| chr14:30715792
|
TCA | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(10): Show | 13 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1630-129_1630-128d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 30715792 | |||||
| chr14:30716303
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1683+326A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716303 | ||||||
| chr14:30716346
|
A | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1683+369A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716346 | ||||||
| chr14:30716471
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1683+494G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716471 | ||||||
| chr14:30716581
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1683+604G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716581 | ||||||
| chr14:30716591
|
G | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1683+614G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716591 | ||||||
| chr14:30716611
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1683+634T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716611 | ||||||
| chr14:30716676
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1683+699A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716676 | ||||||
| chr14:30716765
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1683+788T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30716765 | ||||||
| chr14:30716827
|
CAA | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0208others(3): Show | 6 | HG02886.hp2 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1683+852_1683+853d others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 30716827 | |||||
| chr14:30717278
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1683+1301C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717278 | ||||||
| chr14:30717291
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1683+1314T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717291 | ||||||
| chr14:30717468
|
C | A | 9 | a0002c0002t0001g0248a0002c0002t0001g0261a0002c0002t0001g0265others(6): Show | 9 | HG02129.hp1 NA18944.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1683+1491C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717468 | ||||||
| chr14:30717505
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1683+1528T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717505 | ||||||
| chr14:30717582
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1683+1605T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717582 | ||||||
| chr14:30717622
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(20): Show | 24 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1683+1645T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717622 | ||||||
| chr14:30717625
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1683+1648T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717625 | ||||||
| chr14:30717701
|
G | A | 2 | a0003c0005t0002g0146a0003c0005t0002g0147 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1684-1624G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717701 | ||||||
| chr14:30717750
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1684-1575G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717750 | ||||||
| chr14:30717889
|
A | AAAG | 7 | a0002c0002t0001g0019a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1684-1433_1684-143 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 30717889 | |||||
| chr14:30717892
|
GA | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0151a0001c0001t0001g0152others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1684-1418delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 30717892 | |||||
| chr14:30717894
|
A | AG | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1684-1431_1684-143 others(5): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717894 | ||||||
| chr14:30717985
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684-1340A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30717985 | ||||||
| chr14:30718173
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1684-1152A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718173 | ||||||
| chr14:30718636
|
A | G | 1 | a0002c0002t0001g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1684-689A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718636 | ||||||
| chr14:30718702
|
C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0012t0001g0210 | 3 | HG02886.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1684-623C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718702 | ||||||
| chr14:30718797
|
G | C | 132 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(129): Show | 132 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1684-528G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718797 | ||||||
| chr14:30718883
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1684-442T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718883 | ||||||
| chr14:30718963
|
C | T | 2 | a0002c0002t0001g0223a0002c0002t0001g0251 | 2 | NA18946.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1684-362C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718963 | ||||||
| chr14:30718972
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1684-353T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30718972 | ||||||
| chr14:30719177
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1684-148G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30719177 | ||||||
| chr14:30719191
|
C | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG03654.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1684-134C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30719191 | ||||||
| chr14:30719199
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1684-126G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30719199 | ||||||
| chr14:30719208
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1684-117A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30719208 | ||||||
| chr14:30719299
|
T | C | 2 | a0001c0001t0001g0189a0002c0002t0001g0298 | 2 | HG02293.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1684-26T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 20/24 | chr14 | 30719299 | ||||||
| chr14:30719433
|
T | A | 1 | a0002c0002t0001g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1736+56T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719433 | ||||||
| chr14:30719489
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1736+112G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719489 | ||||||
| chr14:30719626
|
G | A | 85 | a0001c0001t0001g0216a0002c0002t0001g0217a0002c0002t0001g0220others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1736+249G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719626 | ||||||
| chr14:30719627
|
G | A | 42 | a0002c0002t0001g0220a0002c0002t0001g0226a0002c0002t0001g0228others(39): Show | 42 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1736+250G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719627 | ||||||
| chr14:30719696
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1736+319G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719696 | ||||||
| chr14:30719906
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1736+529G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719906 | ||||||
| chr14:30719927
|
C | T | 20 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0039others(17): Show | 20 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1736+550C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719927 | ||||||
| chr14:30719967
|
G | A | 1 | a0002c0002t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1736+590G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719967 | ||||||
| chr14:30719989
|
C | T | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1736+612C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30719989 | ||||||
| chr14:30720084
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1736+707A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720084 | ||||||
| chr14:30720116
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1736+739A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720116 | ||||||
| chr14:30720309
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1736+932A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720309 | ||||||
| chr14:30720636
|
A | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737-1248A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720636 | ||||||
| chr14:30720696
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737-1188A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720696 | ||||||
| chr14:30720720
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1737-1164G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720720 | ||||||
| chr14:30720875
|
G | A | 1 | a0002c0002t0001g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1737-1009G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720875 | ||||||
| chr14:30720924
|
A | T | 1 | a0002c0002t0001g0307 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1737-960A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30720924 | ||||||
| chr14:30721142
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1737-742A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30721142 | ||||||
| chr14:30721159
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1737-725T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30721159 | ||||||
| chr14:30721323
|
T | TGTAA | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1737-558_1737-555d others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 30721323 | |||||
| chr14:30721438
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1737-446C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30721438 | ||||||
| chr14:30721439
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.1737-445A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30721439 | ||||||
| chr14:30721481
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1737-403A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | chr14 | 30721481 | ||||||
| chr14:30721589
|
T | TA | 4 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0305others(1): Show | 4 | HG00642.hp1 HG01496.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737-294dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 30721589 | |||||
| chr14:30722236
|
C | T | 5 | a0003c0004t0002g0148a0003c0004t0002g0149a0003c0004t0002g0150others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1771-258C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | chr14 | 30722236 | ||||||
| chr14:30722273
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1771-221T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | chr14 | 30722273 | ||||||
| chr14:30722405
|
CT | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1771-85delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 30722405 | |||||
| chr14:30722425
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1771-69A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | chr14 | 30722425 | ||||||
| chr14:30722462
|
G | GT | 51 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1771-19dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 30722462 | |||||
| chr14:30722465
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1771-29T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 22/24 | chr14 | 30722465 | ||||||
| chr14:30722566
|
T | C | 77 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(74): Show |
splice_region_variant&intron_variant | LOW | c.1836+7T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30722566 | ||||||
| chr14:30722823
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1836+264A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30722823 | ||||||
| chr14:30722842
|
C | CA | 25 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(22): Show | 25 | HG01243.hp2 HG01358.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1836+295dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30722842 | |||||
| chr14:30722959
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1836+400T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30722959 | ||||||
| chr14:30723290
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1836+731G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30723290 | ||||||
| chr14:30723446
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1836+887G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30723446 | ||||||
| chr14:30723549
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1836+990C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30723549 | ||||||
| chr14:30724012
|
C | CA | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 230 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(227): Show |
intron_variant | MODIFIER | c.1836+1453_1836+145 others(5): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724012 | ||||||
| chr14:30724072
|
T | TA | 121 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1836+1537dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724072
|
T | TAA | 29 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0030others(26): Show | 30 | HG00639.hp2 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1836+1536_1836+153 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724072
|
T | TAAA | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(4): Show | 7 | HG00735.hp1 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+1535_1836+153 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724072
|
T | TAAAA | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+1534_1836+153 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724072
|
TA | T | 7 | a0001c0001t0001g0118a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01070.hp1 HG01070.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+1537delA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724072
|
TAAAAA | T | 40 | a0002c0002t0001g0220a0002c0002t0001g0226a0002c0002t0001g0245others(37): Show | 40 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1836+1533_1836+153 others(9): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724072 | |||||
| chr14:30724123
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0167others(21): Show | 25 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1836+1564A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724123 | ||||||
| chr14:30724245
|
G | GT | 68 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0119others(65): Show | 68 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1836+1713dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724245 | |||||
| chr14:30724245
|
G | GTT | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0167others(16): Show | 19 | HG01891.hp1 HG01934.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1836+1712_1836+171 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724245 | |||||
| chr14:30724245
|
G | GTTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 7 | HG01106.hp2 HG01952.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+1711_1836+171 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724245 | |||||
| chr14:30724245
|
GT | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1836+1713delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724245 | |||||
| chr14:30724245
|
GTTTT | G | 8 | a0002c0002t0001g0019a0002c0002t0001g0201a0002c0002t0001g0202others(5): Show | 8 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+1710_1836+171 others(8): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30724245 | |||||
| chr14:30724261
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1836+1702T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724261 | ||||||
| chr14:30724297
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+1738G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724297 | ||||||
| chr14:30724398
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1836+1839G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724398 | ||||||
| chr14:30724455
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1836+1896G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724455 | ||||||
| chr14:30724460
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1836+1901C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724460 | ||||||
| chr14:30724469
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1836+1910T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724469 | ||||||
| chr14:30724629
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1836+2070C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724629 | ||||||
| chr14:30724708
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1836+2149T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724708 | ||||||
| chr14:30724781
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+2222A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724781 | ||||||
| chr14:30724782
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1836+2223T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724782 | ||||||
| chr14:30724851
|
T | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | NA18942.hp2 NA18954.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+2292T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724851 | ||||||
| chr14:30724945
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1836+2386C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30724945 | ||||||
| chr14:30725008
|
T | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+2449T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725008 | ||||||
| chr14:30725318
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+2759A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725318 | ||||||
| chr14:30725323
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1836+2764A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725323 | ||||||
| chr14:30725325
|
G | A | 1 | a0001c0012t0001g0210 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1836+2766G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725325 | ||||||
| chr14:30725380
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | NA19057.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1836+2821T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725380 | ||||||
| chr14:30725416
|
T | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.1836+2857T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725416 | ||||||
| chr14:30725434
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1836+2875C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725434 | ||||||
| chr14:30725699
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1836+3140T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725699 | ||||||
| chr14:30725743
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.1836+3184A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725743 | ||||||
| chr14:30725785
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.1836+3226G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725785 | ||||||
| chr14:30725835
|
AG | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1836+3277delG | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725835 | ||||||
| chr14:30725973
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1836+3414G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30725973 | ||||||
| chr14:30726049
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1836+3490C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726049 | ||||||
| chr14:30726050
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | NA18942.hp2 NA18954.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+3491G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726050 | ||||||
| chr14:30726057
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1836+3498A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726057 | ||||||
| chr14:30726070
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1836+3511C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726070 | ||||||
| chr14:30726156
|
C | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 38 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1836+3597C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726156 | ||||||
| chr14:30726200
|
T | TA | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1836+3648dupA | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30726200 | |||||
| chr14:30726556
|
TG | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1836+3998delG | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726556 | ||||||
| chr14:30726664
|
C | T | 15 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 15 | HG01074.hp1 HG01099.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1836+4105C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726664 | ||||||
| chr14:30726673
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1836+4114T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726673 | ||||||
| chr14:30726720
|
T | G | 1 | a0002c0002t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1836+4161T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726720 | ||||||
| chr14:30726855
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1836+4296G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726855 | ||||||
| chr14:30726899
|
A | G | 83 | a0001c0001t0001g0216a0002c0002t0001g0217a0002c0002t0001g0220others(80): Show | 83 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1836+4340A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726899 | ||||||
| chr14:30726918
|
A | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02622.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1836+4359A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726918 | ||||||
| chr14:30726953
|
A | G | 1 | a0001c0001t0001g0001 | 2 | NA18953.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1836+4394A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30726953 | ||||||
| chr14:30727040
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+4481G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727040 | ||||||
| chr14:30727090
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1836+4531T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727090 | ||||||
| chr14:30727094
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1836+4535T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727094 | ||||||
| chr14:30727207
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1836+4648A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727207 | ||||||
| chr14:30727311
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1836+4752G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727311 | ||||||
| chr14:30727514
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1836+4955C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727514 | ||||||
| chr14:30727541
|
A | G | 2 | a0001c0001t0001g0022a0001c0011t0001g0036 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1836+4982A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727541 | ||||||
| chr14:30727565
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1836+5006T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727565 | ||||||
| chr14:30727684
|
AGACTTTT others(1650): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1836+5129_1837-544 others(4): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30727684 | |||||
| chr14:30727754
|
C | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 181 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.1836+5195C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727754 | ||||||
| chr14:30727820
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 217 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.1836+5261T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30727820 | ||||||
| chr14:30728221
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1836+5662A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728221 | ||||||
| chr14:30728244
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1836+5685T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728244 | ||||||
| chr14:30728607
|
C | T | 138 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.1836+6048C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728607 | ||||||
| chr14:30728612
|
C | G | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1836+6053C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728612 | ||||||
| chr14:30728783
|
T | A | 3 | a0002c0002t0001g0303a0002c0002t0001g0304a0002c0002t0001g0306 | 3 | HG00642.hp1 HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1837-6007T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728783 | ||||||
| chr14:30728838
|
C | CT | 127 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(124): Show | 127 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1837-5934dupT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30728838 | |||||
| chr14:30728838
|
C | CTT | 14 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0080others(11): Show | 14 | HG00673.hp1 HG00741.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-5935_1837-593 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30728838 | |||||
| chr14:30728838
|
CT | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0030others(28): Show | 32 | HG00558.hp2 HG01106.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1837-5934delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30728838 | |||||
| chr14:30728838
|
CTT | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-5935_1837-593 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30728838 | |||||
| chr14:30728852
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(20): Show | 24 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-5938T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728852 | ||||||
| chr14:30728855
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-5935T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728855 | ||||||
| chr14:30728856
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837-5934T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728856 | ||||||
| chr14:30728856
|
TC | T | 24 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0151others(21): Show | 24 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-5928delC | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30728856 | |||||
| chr14:30728857
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1837-5933C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728857 | ||||||
| chr14:30728868
|
G | A | 1 | a0003c0004t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1837-5922G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728868 | ||||||
| chr14:30728932
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1837-5858C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30728932 | ||||||
| chr14:30729151
|
G | T | 2 | a0001c0001t0001g0022a0001c0011t0001g0036 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1837-5639G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729151 | ||||||
| chr14:30729233
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1837-5557C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729233 | ||||||
| chr14:30729247
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-5543G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729247 | ||||||
| chr14:30729250
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1837-5540G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729250 | ||||||
| chr14:30729385
|
G | A | 1 | a0002c0002t0001g0218 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1837-5405G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729385 | ||||||
| chr14:30729662
|
C | G | 3 | a0003c0004t0002g0148a0003c0005t0002g0146a0003c0005t0002g0147 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1837-5128C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729662 | ||||||
| chr14:30729666
|
T | G | 1 | a0006c0008t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1837-5124T>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729666 | ||||||
| chr14:30729869
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1837-4921A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729869 | ||||||
| chr14:30729869
|
AT | A | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0039others(23): Show | 26 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1837-4909delT | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30729869 | |||||
| chr14:30729869
|
ATT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1837-4910_1837-490 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30729869 | |||||
| chr14:30729903
|
C | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.1837-4887C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729903 | ||||||
| chr14:30729953
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1837-4837C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30729953 | ||||||
| chr14:30730006
|
C | T | 1 | a0002c0002t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1837-4784C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730006 | ||||||
| chr14:30730308
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | NA18942.hp2 NA18954.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-4482G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730308 | ||||||
| chr14:30730319
|
AC | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1837-4469delC | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30730319 | |||||
| chr14:30730333
|
C | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1837-4457C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730333 | ||||||
| chr14:30730521
|
T | C | 1 | a0002c0002t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1837-4269T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730521 | ||||||
| chr14:30730526
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(20): Show | 24 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-4264C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730526 | ||||||
| chr14:30730636
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1837-4154G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730636 | ||||||
| chr14:30730651
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0087 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1837-4139G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730651 | ||||||
| chr14:30730854
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1837-3936G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730854 | ||||||
| chr14:30730929
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 218 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.1837-3861T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730929 | ||||||
| chr14:30730954
|
G | T | 39 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0095others(36): Show | 39 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1837-3836G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30730954 | ||||||
| chr14:30731030
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18965.hp2 NA18967.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1837-3760G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731030 | ||||||
| chr14:30731083
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1837-3707C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731083 | ||||||
| chr14:30731133
|
T | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1837-3657T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731133 | ||||||
| chr14:30731185
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1837-3605G>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731185 | ||||||
| chr14:30731201
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(44): Show | 48 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1837-3589C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731201 | ||||||
| chr14:30731324
|
G | T | 1 | a0002c0002t0001g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1837-3466G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731324 | ||||||
| chr14:30731633
|
T | C | 1 | a0002c0002t0001g0269 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1837-3157T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731633 | ||||||
| chr14:30731866
|
C | T | 1 | a0002c0002t0001g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1837-2924C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731866 | ||||||
| chr14:30731889
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0052others(3): Show | 6 | NA18612.hp1 NA18970.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-2901T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731889 | ||||||
| chr14:30731902
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1837-2888A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731902 | ||||||
| chr14:30731922
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1837-2868G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731922 | ||||||
| chr14:30731948
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1837-2842G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30731948 | ||||||
| chr14:30732023
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0035 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1837-2767G>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30732023 | ||||||
| chr14:30732088
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1837-2702A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30732088 | ||||||
| chr14:30732231
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1837-2559A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30732231 | ||||||
| chr14:30732370
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1837-2420C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30732370 | ||||||
| chr14:30732607
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1837-2183C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30732607 | ||||||
| chr14:30733010
|
C | CTT | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(10): Show | 13 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1837-1768_1837-176 others(6): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30733010 | |||||
| chr14:30733010
|
C | CTTT | 23 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(20): Show | 24 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-1769_1837-176 others(7): Show |
SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 30733010 | |||||
| chr14:30733264
|
T | C | 2 | a0003c0004t0002g0149a0003c0004t0002g0150 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1837-1526T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30733264 | ||||||
| chr14:30733300
|
G | A | 3 | a0002c0002t0001g0230a0002c0002t0001g0231a0002c0002t0001g0232 | 3 | HG00558.hp2 HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1837-1490G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30733300 | ||||||
| chr14:30733534
|
A | G | 77 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1837-1256A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30733534 | ||||||
| chr14:30733859
|
C | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-931C>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30733859 | ||||||
| chr14:30733875
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(5): Show | 8 | HG01074.hp1 HG01099.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-915A>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30733875 | ||||||
| chr14:30734055
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1837-735C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734055 | ||||||
| chr14:30734057
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1837-733A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734057 | ||||||
| chr14:30734097
|
A | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1837-693A>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734097 | ||||||
| chr14:30734160
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-630G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734160 | ||||||
| chr14:30734246
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1837-544G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734246 | ||||||
| chr14:30734332
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1837-458A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734332 | ||||||
| chr14:30734378
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1837-412A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734378 | ||||||
| chr14:30734392
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1837-398C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734392 | ||||||
| chr14:30734599
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 37 | HG01106.hp2 HG01884.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1837-191A>G | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734599 | ||||||
| chr14:30734604
|
C | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-186C>T | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734604 | ||||||
| chr14:30734664
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0169others(18): Show | 22 | HG01106.hp2 HG01928.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1837-126T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 23/24 | chr14 | 30734664 | ||||||
| chr14:30734946
|
T | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0201others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1905+88T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30734946 | ||||||
| chr14:30735058
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1905+200T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30735058 | ||||||
| chr14:30735227
|
G | A | 153 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(150): Show | 153 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1906-359G>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30735227 | ||||||
| chr14:30735230
|
A | AC | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906-354dupC | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 30735230 | |||||
| chr14:30735499
|
T | A | 1 | a0002c0002t0001g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1906-87T>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30735499 | ||||||
| chr14:30735503
|
T | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02630.hp1 HG03704.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-83T>C | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30735503 | ||||||
| chr14:30735515
|
C | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0002t0001g0019others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1906-71C>A | SCFD1 | ENSG00000092108.22 | transcript | ENST00000458591.7 | protein_coding | 24/24 | chr14 | 30735515 |