| geneid | 64093 |
|---|---|
| ensemblid | ENSG00000198732.11 |
| hgncid | 20318 |
| symbol | SMOC1 |
| name | SPARC related modular calcium binding 1 |
| refseq_nuc | NM_001034852.3 |
| refseq_prot | NP_001030024.1 |
| ensembl_nuc | ENST00000361956.8 |
| ensembl_prot | ENSP00000355110.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 69879416 |
| end | 70032366 |
| strand | + |
| ver | v1.2 |
| region | chr14:69879416-70032366 |
| region5000 | chr14:69874416-70037366 |
| regionname0 | SMOC1_chr14_69879416_70032366 |
| regionname5000 | SMOC1_chr14_69874416_70037366 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 435 | 265 | 89 | 57 | 75 | 14 | 28 | 60 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0002 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0003 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0004 | 0/0 | 435 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0005 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0006 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1308 | 205 | 80 | 45 | 45 | 11 | 22 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0002 | 0/0 | 1308 | 37 | 0 | 8 | 23 | 2 | 4 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0003 | 0/0 | 1308 | 8 | 0 | 0 | 7 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0004 | 0/0 | 1308 | 5 | 2 | 1 | 0 | 1 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0005 | 0/0 | 1308 | 4 | 4 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0006 | 0/0 | 1308 | 3 | 1 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0007 | 0/0 | 1308 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0008 | 0/0 | 1308 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0009 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0010 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0011 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0012 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| c0013 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| 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 | 2372 | 146 | 55 | 36 | 32 | 7 | 14 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0002 | 0/0 | 2372 | 44 | 0 | 10 | 29 | 2 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0003 | 0/0 | 2372 | 13 | 4 | 0 | 7 | 2 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0004 | 0/0 | 2372 | 8 | 0 | 0 | 4 | 1 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0005 | 0/0 | 2372 | 8 | 4 | 1 | 0 | 0 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0006 | 0/0 | 2372 | 7 | 1 | 1 | 0 | 2 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0007 | 0/0 | 2372 | 6 | 6 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0008 | 0/0 | 2372 | 4 | 4 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0009 | 0/0 | 2372 | 3 | 2 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0010 | 0/0 | 2372 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0011 | 0/0 | 2372 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0012 | 0/0 | 2372 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0013 | 0/0 | 2372 | 2 | 0 | 1 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0014 | 0/0 | 2372 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0015 | 0/0 | 2372 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0016 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0017 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0018 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0019 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0020 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0021 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0022 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0023 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0024 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0025 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0026 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0027 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0028 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0029 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0030 | 0/0 | 2372 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0031 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0032 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0033 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| t0034 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| 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 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1308 | 205 | 80 | 45 | 45 | 11 | 22 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002 | 0/0 | 1308 | 37 | 0 | 8 | 23 | 2 | 4 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0003 | 0/0 | 1308 | 8 | 0 | 0 | 7 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0004 | 0/0 | 1308 | 5 | 2 | 1 | 0 | 1 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0005 | 0/0 | 1308 | 4 | 4 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0006 | 0/0 | 1308 | 3 | 1 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0007 | 0/0 | 1308 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0011 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0002c0013 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0003c0009 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0004c0012 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0005c0008 | 0/0 | 1308 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0006c0010 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3679 | 130 | 48 | 32 | 28 | 7 | 13 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0002 | 0/0 | 3679 | 7 | 0 | 2 | 5 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0003 | 0/0 | 3679 | 12 | 3 | 0 | 7 | 2 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0004 | 0/0 | 3679 | 6 | 0 | 0 | 4 | 0 | 2 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0005 | 0/0 | 3679 | 7 | 4 | 1 | 0 | 0 | 2 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0006 | 0/0 | 3679 | 5 | 0 | 0 | 0 | 2 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0007 | 0/0 | 3679 | 6 | 6 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0008 | 0/0 | 3679 | 4 | 4 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0009 | 0/0 | 3679 | 3 | 2 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0010 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0011 | 0/0 | 3679 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0012 | 0/0 | 3679 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0013 | 0/0 | 3679 | 2 | 0 | 1 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0014 | 0/0 | 3679 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0015 | 0/0 | 3679 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0016 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0017 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0018 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0019 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0020 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0021 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0022 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0026 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0027 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0029 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0030 | 0/0 | 3679 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0031 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0032 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0001t0033 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002t0001 | 0/0 | 3679 | 3 | 0 | 0 | 2 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002t0002 | 0/0 | 3679 | 31 | 0 | 8 | 18 | 2 | 3 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002t0024 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002t0025 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0002t0028 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0003t0001 | 0/0 | 3679 | 2 | 0 | 0 | 2 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0003t0002 | 0/0 | 3679 | 5 | 0 | 0 | 5 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0003t0004 | 0/0 | 3679 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0004t0001 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0004t0004 | 0/0 | 3679 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0004t0005 | 0/0 | 3679 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0004t0006 | 0/0 | 3679 | 2 | 1 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0005t0001 | 0/0 | 3679 | 3 | 3 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0005t0010 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0006t0001 | 0/0 | 3679 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0006t0034 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0007t0001 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0007t0003 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0001c0011t0001 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0002c0013t0023 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0003c0009t0001 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0004c0012t0001 | 0/0 | 3679 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0005c0008t0002 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| a0006c0010t0001 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | copy fasta | chr14 | 69874416 | 70037366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0013g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0014g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0014g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0017g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0018g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0022g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0026g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0029g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0030g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0032g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0001t0033g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0024g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0025g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0002t0028g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0004t0005g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0004t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0004t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0005t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0006t0034g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0007t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0001c0011t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0002c0013t0023g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0003c0009t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0004c0012t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0005c0008t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| a0006c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0250 | EUR | GBR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0023 | EUR | GBR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | FIN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0210 | EUR | FIN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0141 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0236 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00642 | hp2 | a0001 | c0006 | t0001 | g0233 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01081 | hp2 | a0001 | c0004 | t0006 | g0201 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01099 | hp1 | a0001 | c0006 | t0001 | g0220 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01106 | hp1 | a0001 | c0001 | t0018 | g0148 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0178 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0176 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01168 | hp1 | a0001 | c0001 | t0014 | g0173 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0099 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0037 | AMR | PUR | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01346 | hp1 | a0004 | c0012 | t0001 | g0107 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0212 | EUR | IBS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0230 | EUR | IBS | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01884 | hp2 | a0001 | c0001 | t0031 | g0053 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01934 | hp1 | a0001 | c0001 | t0032 | g0170 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02015 | hp2 | a0005 | c0008 | t0002 | g0251 | EAS | KHV | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0265 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0246 | EAS | KHV | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0122 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PEL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02258 | hp2 | a0001 | c0001 | t0033 | g0043 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02280 | hp2 | a0002 | c0013 | t0023 | g0027 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02572 | hp2 | a0001 | c0005 | t0010 | g0101 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02602 | hp2 | a0001 | c0001 | t0030 | g0093 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0095 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02630 | hp1 | a0001 | c0006 | t0034 | g0092 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0062 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02735 | hp2 | a0001 | c0001 | t0013 | g0147 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0175 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0069 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02922 | hp2 | a0001 | c0001 | t0027 | g0036 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02965 | hp2 | a0001 | c0001 | t0020 | g0096 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03017 | hp2 | a0001 | c0003 | t0004 | g0120 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0078 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03130 | hp1 | a0001 | c0001 | t0026 | g0072 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0094 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03579 | hp2 | a0006 | c0010 | t0001 | g0035 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0080 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | PJL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | STU | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | BEB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG04228 | hp2 | a0001 | c0004 | t0005 | g0024 | SAS | STU | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0106 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18612 | hp2 | a0001 | c0002 | t0024 | g0133 | EAS | CHB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | CHB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18993 | hp1 | a0001 | c0001 | t0029 | g0021 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19002 | hp2 | a0001 | c0002 | t0028 | g0223 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19005 | hp1 | a0001 | c0002 | t0025 | g0240 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0145 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19030 | hp2 | a0001 | c0007 | t0003 | g0008 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0124 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19089 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0040 | AFR | YRI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | ASW | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20129 | hp2 | a0001 | c0004 | t0006 | g0202 | AFR | ASW | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20752 | hp1 | a0001 | c0004 | t0004 | g0105 | EUR | TSI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG01123 | hp2 | a0001 | c0011 | t0001 | g0252 | AMR | CLM | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02109 | hp2 | a0003 | c0009 | t0001 | g0045 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0054 | AFR | ACB | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | USA | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0064 | AFR | USA | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0153 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0081 | REF | REF | SMOC1_chr14_69874416_70037366 | SMOC1 | chr14 | 69874416 | 70037366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69952201
|
A | T | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.163A>T | p.Ile55Phe | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/12 | 426/3679 | 163/1308 | 55/435 | chr14 | 69952201 | ||
| chr14:69952282
|
G | A | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.244G>A | p.Val82Met | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/12 | 507/3679 | 244/1308 | 82/435 | chr14 | 69952282 | ||
| chr14:69952291
|
G | C | 1 | a0006 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.253G>C | p.Gly85Arg | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/12 | 516/3679 | 253/1308 | 85/435 | chr14 | 69952291 | ||
| chr14:70011513
|
G | A | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.886G>A | p.Ala296Thr | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/12 | 1149/3679 | 886/1308 | 296/435 | chr14 | 70011513 | ||
| chr14:70011525
|
A | G | 1 | a0004 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.898A>G | p.Thr300Ala | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/12 | 1161/3679 | 898/1308 | 300/435 | chr14 | 70011525 | ||
| chr14:70023280
|
G | A | 1 | a0005 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1124G>A | p.Ser375Asn | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/12 | 1387/3679 | 1124/1308 | 375/435 | chr14 | 70023280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69952164
|
G | A | 3 | a0001c0002a0001c0004a0005c0008 | 43 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(40): Show |
synonymous_variant | LOW | c.126G>A | p.Gln42Gln | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/12 | 389/3679 | 126/1308 | 42/435 | chr14 | 69952164 | ||
| chr14:70010791
|
C | T | 3 | a0001c0002a0001c0003a0005c0008 | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
synonymous_variant | LOW | c.702C>T | p.Ala234Ala | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/12 | 965/3679 | 702/1308 | 234/435 | chr14 | 70010791 | ||
| chr14:70013427
|
C | T | 1 | a0001c0006 | 3 | HG00642.hp2 HG01099.hp1 HG02630.hp1 |
synonymous_variant | LOW | c.982C>T | p.Leu328Leu | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/12 | 1245/3679 | 982/1308 | 328/435 | chr14 | 70013427 | ||
| chr14:70023317
|
C | T | 1 | a0001c0005 | 4 | HG02572.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.1161C>T | p.Phe387Phe | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/12 | 1424/3679 | 1161/1308 | 387/435 | chr14 | 70023317 | ||
| chr14:70023404
|
T | C | 1 | a0001c0007 | 2 | NA19030.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.1248T>C | p.Ile416Ile | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/12 | 1511/3679 | 1248/1308 | 416/435 | chr14 | 70023404 | ||
| chr14:70030252
|
C | T | 1 | a0001c0011 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1302C>T | p.Leu434Leu | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1565/3679 | 1302/1308 | 434/435 | chr14 | 70030252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69879420
|
G | A | 2 | a0001c0001t0010a0001c0005t0010 | 2 | HG01192.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-259G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 259 | chr14 | 69879420 | |||||
| chr14:69879427
|
C | T | 1 | a0001c0006t0034 | 1 | HG02630.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | chr14 | 69879427 | ||||||
| chr14:69879445
|
C | A | 2 | a0001c0001t0011a0001c0001t0016 | 3 | HG01175.hp2 HG03098.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-234C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 234 | chr14 | 69879445 | |||||
| chr14:69879489
|
C | T | 1 | a0001c0001t0033 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 190 | chr14 | 69879489 | |||||
| chr14:69879596
|
G | C | 1 | a0001c0001t0012 | 2 | HG01069.hp1 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-83G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 83 | chr14 | 69879596 | |||||
| chr14:69879596
|
G | T | 1 | a0001c0001t0032 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 83 | chr14 | 69879596 | |||||
| chr14:69879633
|
G | A | 3 | a0001c0001t0013a0001c0001t0017a0001c0001t0018 | 4 | HG01106.hp1 HG01109.hp1 HG01109.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/12 | 46 | chr14 | 69879633 | |||||
| chr14:70030338
|
A | G | 4 | a0001c0001t0005a0001c0001t0018a0001c0001t0031others(1): Show | 10 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*80A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 80 | chr14 | 70030338 | |||||
| chr14:70030356
|
G | A | 1 | a0001c0001t0019 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 98 | chr14 | 70030356 | |||||
| chr14:70030471
|
G | A | 1 | a0001c0001t0020 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 213 | chr14 | 70030471 | |||||
| chr14:70030550
|
T | G | 1 | a0001c0001t0033 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 292 | chr14 | 70030550 | |||||
| chr14:70030664
|
C | A | 1 | a0001c0001t0014 | 2 | HG01168.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 406 | chr14 | 70030664 | |||||
| chr14:70030818
|
G | A | 3 | a0001c0001t0004a0001c0003t0004a0001c0004t0004 | 8 | HG02735.hp1 HG03017.hp2 HG03927.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*560G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 560 | chr14 | 70030818 | |||||
| chr14:70030829
|
T | C | 1 | a0001c0001t0021 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 571 | chr14 | 70030829 | |||||
| chr14:70030984
|
C | T | 2 | a0001c0001t0020a0001c0001t0030 | 2 | HG02602.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*726C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 726 | chr14 | 70030984 | |||||
| chr14:70031001
|
G | A | 1 | a0001c0001t0007 | 6 | HG02055.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 743 | chr14 | 70031001 | |||||
| chr14:70031017
|
C | T | 1 | a0001c0001t0008 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*759C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 759 | chr14 | 70031017 | |||||
| chr14:70031018
|
G | A | 3 | a0001c0001t0005a0001c0001t0018a0001c0004t0005 | 9 | HG01106.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 760 | chr14 | 70031018 | |||||
| chr14:70031094
|
T | C | 1 | a0001c0001t0022 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 836 | chr14 | 70031094 | |||||
| chr14:70031185
|
A | G | 1 | a0001c0001t0029 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*927A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 927 | chr14 | 70031185 | |||||
| chr14:70031303
|
C | T | 1 | a0001c0002t0028 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1045 | chr14 | 70031303 | |||||
| chr14:70031424
|
G | A | 2 | a0001c0001t0006a0001c0004t0006 | 7 | HG00323.hp2 HG01081.hp2 HG01517.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1166G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1166 | chr14 | 70031424 | |||||
| chr14:70031472
|
T | C | 1 | a0002c0013t0023 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1214 | chr14 | 70031472 | |||||
| chr14:70031617
|
A | G | 1 | a0001c0001t0007 | 6 | HG02055.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1359A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1359 | chr14 | 70031617 | |||||
| chr14:70031636
|
G | A | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0026others(8): Show | 56 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1378 | chr14 | 70031636 | |||||
| chr14:70031690
|
C | T | 3 | a0001c0001t0003a0001c0001t0021a0001c0007t0003 | 14 | HG00140.hp1 HG00323.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1432C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1432 | chr14 | 70031690 | |||||
| chr14:70031743
|
G | A | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1485G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1485 | chr14 | 70031743 | |||||
| chr14:70031786
|
A | G | 1 | a0001c0001t0009 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1528A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1528 | chr14 | 70031786 | |||||
| chr14:70031858
|
A | T | 1 | a0001c0001t0026 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1600A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1600 | chr14 | 70031858 | |||||
| chr14:70031974
|
C | T | 1 | a0001c0002t0025 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 1716 | chr14 | 70031974 | |||||
| chr14:70032289
|
T | C | 1 | a0001c0002t0024 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2031T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 2031 | chr14 | 70032289 | |||||
| chr14:70032301
|
T | A | 3 | a0001c0001t0015a0001c0001t0016a0001c0001t0017 | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2043T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 12/12 | 2043 | chr14 | 70032301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69879972
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0131others(135): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.99+195C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69879972 | ||||||
| chr14:69880015
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99+238G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880015 | ||||||
| chr14:69880110
|
G | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(173): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.99+333G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880110 | ||||||
| chr14:69880137
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0008g0002others(1): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+360G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880137 | ||||||
| chr14:69880352
|
AC | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0008g0002others(1): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+576delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880352 | ||||||
| chr14:69880377
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+600T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880377 | ||||||
| chr14:69880540
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+763A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880540 | ||||||
| chr14:69880573
|
A | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+796A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880573 | ||||||
| chr14:69880583
|
A | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+806A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880583 | ||||||
| chr14:69880584
|
C | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+807C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880584 | ||||||
| chr14:69880631
|
A | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0123a0001c0001t0001g0130others(136): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.99+854A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880631 | ||||||
| chr14:69880655
|
C | T | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+878C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880655 | ||||||
| chr14:69880735
|
A | G | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.99+958A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880735 | ||||||
| chr14:69880798
|
T | C | 1 | a0001c0002t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.99+1021T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880798 | ||||||
| chr14:69880972
|
T | C | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+1195T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69880972 | ||||||
| chr14:69881099
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+1322G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881099 | ||||||
| chr14:69881171
|
T | C | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99+1394T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881171 | ||||||
| chr14:69881315
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+1538C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881315 | ||||||
| chr14:69881316
|
G | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0112others(10): Show | 14 | HG00280.hp1 HG00639.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+1539G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881316 | ||||||
| chr14:69881424
|
C | CATAT | 77 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0131others(74): Show | 77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.99+1648_99+1651dup others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69881424 | |||||
| chr14:69881454
|
T | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.99+1677T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881454 | ||||||
| chr14:69881549
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.99+1772A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881549 | ||||||
| chr14:69881549
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.99+1772A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881549 | ||||||
| chr14:69881677
|
A | AAC | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(16): Show | 19 | HG00140.hp2 HG02074.hp1 HG02698.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+1912_99+1913dup others(2): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69881677 | |||||
| chr14:69881837
|
G | A | 24 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(21): Show | 24 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+2060G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881837 | ||||||
| chr14:69881888
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0002c0013t0023g0027 | 3 | HG02280.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+2111G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881888 | ||||||
| chr14:69881922
|
C | T | 2 | a0001c0001t0001g0264a0001c0004t0001g0265 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.99+2145C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69881922 | ||||||
| chr14:69882214
|
C | T | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+2437C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69882214 | ||||||
| chr14:69882215
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0073others(8): Show | 12 | HG01175.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+2438G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69882215 | ||||||
| chr14:69882540
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+2763C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69882540 | ||||||
| chr14:69882666
|
A | AG | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(1): Show | 4 | HG02602.hp1 HG03017.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+2893dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69882666 | |||||
| chr14:69882696
|
C | T | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.99+2919C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69882696 | ||||||
| chr14:69882965
|
C | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0002g0003others(4): Show | 8 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3188C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69882965 | ||||||
| chr14:69883119
|
A | G | 7 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0003g0198others(4): Show | 7 | HG00423.hp1 HG00597.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+3342A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883119 | ||||||
| chr14:69883145
|
A | T | 1 | a0001c0001t0003g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.99+3368A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883145 | ||||||
| chr14:69883750
|
A | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(87): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.99+3973A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883750 | ||||||
| chr14:69883782
|
C | A | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+4005C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883782 | ||||||
| chr14:69883889
|
A | AT | 84 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(81): Show | 85 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.99+4140dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATT | 48 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.99+4139_99+4140dup others(2): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATTT | 26 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 26 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.99+4138_99+4140dup others(3): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATTTT | 34 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0041others(31): Show | 35 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+4137_99+4140dup others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATTTTT | 31 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0026others(28): Show | 32 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+4136_99+4140dup others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATTTTTT | 5 | a0001c0001t0001g0071a0001c0001t0001g0263a0001c0001t0005g0103others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+4135_99+4140dup others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+4130_99+4140dup others(11): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+4112A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883889 | ||||||
| chr14:69883889
|
ATTT | A | 5 | a0001c0001t0001g0098a0001c0001t0007g0097a0001c0001t0010g0099others(2): Show | 5 | HG01192.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4138_99+4140del others(3): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883889
|
ATTTTTTT others(9): Show |
A | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0002g0003others(4): Show | 8 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+4125_99+4140del others(16): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69883889 | |||||
| chr14:69883975
|
T | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.99+4198T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69883975 | ||||||
| chr14:69884000
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+4223G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884000 | ||||||
| chr14:69884172
|
T | C | 133 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.99+4395T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884172 | ||||||
| chr14:69884280
|
T | C | 18 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0073others(15): Show | 20 | HG00738.hp2 HG01069.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+4503T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884280 | ||||||
| chr14:69884302
|
G | GT | 9 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0007g0097others(6): Show | 9 | HG01192.hp2 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+4533dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69884302 | |||||
| chr14:69884343
|
T | C | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+4566T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884343 | ||||||
| chr14:69884617
|
G | A | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+4840G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884617 | ||||||
| chr14:69884872
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(87): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.99+5095T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884872 | ||||||
| chr14:69884873
|
G | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(86): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.99+5096G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884873 | ||||||
| chr14:69884912
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99+5135C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884912 | ||||||
| chr14:69884921
|
T | C | 1 | a0001c0002t0025g0240 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.99+5144T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884921 | ||||||
| chr14:69884948
|
T | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(87): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.99+5171T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69884948 | ||||||
| chr14:69885150
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.99+5373A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885150 | ||||||
| chr14:69885256
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG02698.hp1 HG02738.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5479C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885256 | ||||||
| chr14:69885257
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+5480G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885257 | ||||||
| chr14:69885266
|
C | CT | 19 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(16): Show | 20 | HG01069.hp2 HG01243.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+5504dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69885266 | |||||
| chr14:69885266
|
C | CTT | 69 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0017others(66): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.99+5503_99+5504dup others(2): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69885266 | |||||
| chr14:69885266
|
CT | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0132a0001c0001t0003g0089others(2): Show | 5 | HG01496.hp2 HG02886.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5504delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69885266 | |||||
| chr14:69885383
|
C | T | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+5606C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885383 | ||||||
| chr14:69885384
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0073others(8): Show | 12 | HG01175.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+5607G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885384 | ||||||
| chr14:69885440
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+5663C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885440 | ||||||
| chr14:69885441
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0046others(18): Show | 22 | HG01175.hp2 HG01192.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.99+5664G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885441 | ||||||
| chr14:69885487
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+5710C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885487 | ||||||
| chr14:69885534
|
C | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 23 | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+5757C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885534 | ||||||
| chr14:69885592
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0112others(10): Show | 14 | HG00280.hp1 HG00639.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+5815A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885592 | ||||||
| chr14:69885609
|
C | A | 1 | a0001c0002t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.99+5832C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885609 | ||||||
| chr14:69885648
|
C | A | 1 | a0001c0001t0005g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+5871C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885648 | ||||||
| chr14:69885760
|
G | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.99+5983G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885760 | ||||||
| chr14:69885786
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+6009C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885786 | ||||||
| chr14:69885876
|
G | A | 1 | a0001c0002t0024g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.99+6099G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885876 | ||||||
| chr14:69885966
|
G | A | 3 | a0001c0001t0002g0135a0001c0002t0001g0137a0001c0002t0002g0136 | 3 | NA18956.hp2 NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.99+6189G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69885966 | ||||||
| chr14:69886099
|
C | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0002g0003others(4): Show | 8 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+6322C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69886099 | ||||||
| chr14:69886100
|
G | A | 27 | a0001c0001t0001g0243a0001c0001t0001g0247a0001c0001t0001g0249others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.99+6323G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69886100 | ||||||
| chr14:69886117
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0003g0056others(6): Show | 9 | HG01192.hp2 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+6340C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69886117 | ||||||
| chr14:69886135
|
C | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0002g0003others(4): Show | 8 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+6358C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69886135 | ||||||
| chr14:69886900
|
A | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0086a0001c0001t0001g0087others(17): Show | 21 | HG00280.hp1 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+7123A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69886900 | ||||||
| chr14:69887025
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+7248C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887025 | ||||||
| chr14:69887086
|
G | T | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.99+7309G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887086 | ||||||
| chr14:69887184
|
T | C | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+7407T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887184 | ||||||
| chr14:69887267
|
AG | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0112others(10): Show | 14 | HG00280.hp1 HG00639.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+7492delG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69887267 | |||||
| chr14:69887417
|
G | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0073others(8): Show | 12 | HG01175.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+7640G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887417 | ||||||
| chr14:69887450
|
C | G | 4 | a0001c0001t0005g0189a0001c0001t0007g0032a0001c0001t0007g0034others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7673C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887450 | ||||||
| chr14:69887713
|
G | A | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.99+7936G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887713 | ||||||
| chr14:69887719
|
A | C | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.99+7942A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887719 | ||||||
| chr14:69887772
|
C | T | 7 | a0001c0001t0001g0098a0001c0001t0003g0056a0001c0001t0007g0097others(4): Show | 7 | HG01192.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+7995C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887772 | ||||||
| chr14:69887941
|
C | A | 1 | a0001c0005t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99+8164C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69887941 | ||||||
| chr14:69888011
|
G | C | 1 | a0001c0001t0020g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+8234G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888011 | ||||||
| chr14:69888065
|
G | C | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+8288G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888065 | ||||||
| chr14:69888130
|
G | A | 1 | a0001c0004t0004g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+8353G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888130 | ||||||
| chr14:69888141
|
A | C | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(202): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.99+8364A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888141 | ||||||
| chr14:69888200
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+8423C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888200 | ||||||
| chr14:69888310
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0002c0013t0023g0027 | 3 | HG02280.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+8533C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888310 | ||||||
| chr14:69888420
|
G | C | 4 | a0001c0001t0005g0189a0001c0001t0007g0032a0001c0001t0007g0034others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8643G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888420 | ||||||
| chr14:69888506
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+8729C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888506 | ||||||
| chr14:69888552
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(132): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.99+8775G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888552 | ||||||
| chr14:69888596
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+8819C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888596 | ||||||
| chr14:69888602
|
C | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.99+8825C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888602 | ||||||
| chr14:69888608
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0008g0057 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.99+8831G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888608 | ||||||
| chr14:69888672
|
C | CT | 109 | a0001c0001t0001g0005a0001c0001t0001g0123a0001c0001t0001g0130others(106): Show | 110 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.99+8905dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69888672 | |||||
| chr14:69888848
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02572.hp1 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.99+9071A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888848 | ||||||
| chr14:69888868
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+9091A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888868 | ||||||
| chr14:69888901
|
G | A | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.99+9124G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69888901 | ||||||
| chr14:69889191
|
C | T | 1 | a0001c0002t0002g0012 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.99+9414C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889191 | ||||||
| chr14:69889235
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.99+9458G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889235 | ||||||
| chr14:69889308
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99+9531A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889308 | ||||||
| chr14:69889330
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(45): Show | 48 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.99+9553C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889330 | ||||||
| chr14:69889409
|
G | A | 31 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0140others(28): Show | 31 | HG00558.hp1 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.99+9632G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889409 | ||||||
| chr14:69889451
|
C | A | 38 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0059others(35): Show | 40 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.99+9674C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889451 | ||||||
| chr14:69889494
|
T | G | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.99+9717T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889494 | ||||||
| chr14:69889517
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.99+9740G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889517 | ||||||
| chr14:69889578
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.99+9801A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889578 | ||||||
| chr14:69889645
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(30): Show | 33 | HG00140.hp2 HG00733.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+9868A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889645 | ||||||
| chr14:69889722
|
T | TA | 5 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0013g0147others(2): Show | 5 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9952dupA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69889722 | |||||
| chr14:69889817
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0128a0001c0001t0007g0032others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+10040G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889817 | ||||||
| chr14:69889991
|
G | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(18): Show | 21 | HG00140.hp2 HG00733.hp2 HG02970.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+10214G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69889991 | ||||||
| chr14:69890065
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0087 | 2 | HG01106.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.99+10288C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890065 | ||||||
| chr14:69890066
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+10289G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890066 | ||||||
| chr14:69890095
|
C | A | 1 | a0001c0002t0002g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+10318C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890095 | ||||||
| chr14:69890403
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.99+10626A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890403 | ||||||
| chr14:69890453
|
A | G | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+10676A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890453 | ||||||
| chr14:69890465
|
T | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0065others(35): Show | 39 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+10688T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890465 | ||||||
| chr14:69890524
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+10747C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890524 | ||||||
| chr14:69890672
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.99+10895A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890672 | ||||||
| chr14:69890820
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0008g0062 | 3 | HG02486.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.99+11043A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890820 | ||||||
| chr14:69890885
|
A | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0049others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+11108A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890885 | ||||||
| chr14:69890892
|
T | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(34): Show | 37 | HG00140.hp2 HG00733.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.99+11115T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69890892 | ||||||
| chr14:69891562
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+11785C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891562 | ||||||
| chr14:69891563
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0111others(7): Show | 11 | HG01168.hp1 HG01257.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+11786C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891563 | ||||||
| chr14:69891582
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+11805C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891582 | ||||||
| chr14:69891625
|
G | C | 31 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(28): Show | 33 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+11848G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891625 | ||||||
| chr14:69891634
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.99+11857C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891634 | ||||||
| chr14:69891634
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+11857C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891634 | ||||||
| chr14:69891729
|
T | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 19 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+11952T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891729 | ||||||
| chr14:69891781
|
C | T | 1 | a0001c0001t0003g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.99+12004C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891781 | ||||||
| chr14:69891830
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+12053C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891830 | ||||||
| chr14:69891960
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+12183A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69891960 | ||||||
| chr14:69892009
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+12232A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892009 | ||||||
| chr14:69892020
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0003g0056 | 3 | HG02809.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99+12243T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892020 | ||||||
| chr14:69892104
|
T | C | 8 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0222others(5): Show | 8 | HG00738.hp1 HG01106.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+12327T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892104 | ||||||
| chr14:69892433
|
G | C | 1 | a0001c0001t0006g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+12656G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892433 | ||||||
| chr14:69892438
|
G | T | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+12661G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892438 | ||||||
| chr14:69892538
|
T | C | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+12761T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892538 | ||||||
| chr14:69892602
|
C | G | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+12825C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892602 | ||||||
| chr14:69892733
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+12956T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892733 | ||||||
| chr14:69892908
|
T | C | 32 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 34 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.99+13131T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69892908 | ||||||
| chr14:69893004
|
C | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+13227C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893004 | ||||||
| chr14:69893055
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.99+13278C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893055 | ||||||
| chr14:69893148
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.99+13371G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893148 | ||||||
| chr14:69893332
|
C | T | 1 | a0001c0002t0002g0197 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.99+13555C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893332 | ||||||
| chr14:69893410
|
C | A | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+13633C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893410 | ||||||
| chr14:69893469
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.99+13692A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893469 | ||||||
| chr14:69893518
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99+13741G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893518 | ||||||
| chr14:69893620
|
C | G | 1 | a0001c0001t0022g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+13843C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893620 | ||||||
| chr14:69893808
|
G | A | 88 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(85): Show | 89 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+14031G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893808 | ||||||
| chr14:69893825
|
T | C | 30 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(27): Show | 32 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+14048T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893825 | ||||||
| chr14:69893898
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+14121C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893898 | ||||||
| chr14:69893909
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.99+14132A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893909 | ||||||
| chr14:69893961
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.99+14184C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893961 | ||||||
| chr14:69893975
|
C | T | 12 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0091others(9): Show | 13 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+14198C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893975 | ||||||
| chr14:69893988
|
A | G | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+14211A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69893988 | ||||||
| chr14:69894141
|
T | C | 27 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 29 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+14364T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894141 | ||||||
| chr14:69894145
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 29 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+14368G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894145 | ||||||
| chr14:69894154
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(16): Show | 19 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+14377A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894154 | ||||||
| chr14:69894268
|
G | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(26): Show | 29 | HG00733.hp2 HG01175.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+14491G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894268 | ||||||
| chr14:69894541
|
C | G | 3 | a0001c0001t0005g0219a0001c0006t0001g0220a0001c0006t0001g0233 | 3 | HG00642.hp2 HG01099.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+14764C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894541 | ||||||
| chr14:69894564
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+14787A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894564 | ||||||
| chr14:69894591
|
A | C | 11 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0143others(8): Show | 12 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+14814A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894591 | ||||||
| chr14:69894693
|
G | A | 243 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.99+14916G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894693 | ||||||
| chr14:69894744
|
G | A | 11 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0143others(8): Show | 12 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+14967G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69894744 | ||||||
| chr14:69895068
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02074.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+15291A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895068 | ||||||
| chr14:69895183
|
A | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(12): Show | 15 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+15406A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895183 | ||||||
| chr14:69895208
|
C | T | 3 | a0001c0001t0001g0258a0001c0002t0002g0194a0001c0002t0024g0133 | 3 | HG00597.hp2 NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.99+15431C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895208 | ||||||
| chr14:69895264
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+15487G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895264 | ||||||
| chr14:69895291
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+15514G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895291 | ||||||
| chr14:69895357
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+15580A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895357 | ||||||
| chr14:69895431
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+15654A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895431 | ||||||
| chr14:69895437
|
T | C | 26 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 28 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+15660T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895437 | ||||||
| chr14:69895482
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.99+15705G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895482 | ||||||
| chr14:69895486
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+15709T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895486 | ||||||
| chr14:69895750
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 29 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+15973G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895750 | ||||||
| chr14:69895839
|
C | CT | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+16071dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69895839 | |||||
| chr14:69895867
|
CT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0073others(9): Show | 12 | HG01106.hp2 HG01346.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+16105delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69895867 | |||||
| chr14:69895867
|
CTT | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(137): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.99+16104_99+16105d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69895867 | |||||
| chr14:69895919
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+16142C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69895919 | ||||||
| chr14:69896173
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0005t0001g0033 | 3 | HG02717.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.99+16396C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896173 | ||||||
| chr14:69896174
|
G | A | 1 | a0001c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+16397G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896174 | ||||||
| chr14:69896454
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0128a0001c0001t0007g0032others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+16677T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896454 | ||||||
| chr14:69896473
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+16696T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896473 | ||||||
| chr14:69896532
|
A | G | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+16755A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896532 | ||||||
| chr14:69896607
|
T | C | 37 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(34): Show | 39 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+16830T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896607 | ||||||
| chr14:69896613
|
T | C | 1 | a0001c0001t0031g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+16836T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896613 | ||||||
| chr14:69896752
|
T | C | 43 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0050others(40): Show | 45 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+16975T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896752 | ||||||
| chr14:69896814
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+17037C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69896814 | ||||||
| chr14:69897071
|
C | G | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+17294C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897071 | ||||||
| chr14:69897144
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.99+17367C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897144 | ||||||
| chr14:69897183
|
G | T | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+17406G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897183 | ||||||
| chr14:69897200
|
G | A | 1 | a0001c0001t0029g0021 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.99+17423G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897200 | ||||||
| chr14:69897322
|
T | C | 1 | a0001c0001t0016g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+17545T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897322 | ||||||
| chr14:69897568
|
T | TA | 30 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(27): Show | 32 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+17804dupA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69897568 | |||||
| chr14:69897568
|
TA | T | 30 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(27): Show | 30 | HG00733.hp2 HG01175.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.99+17804delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69897568 | |||||
| chr14:69897655
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.99+17878G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897655 | ||||||
| chr14:69897714
|
C | T | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+17937C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69897714 | ||||||
| chr14:69898052
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 29 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+18275G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898052 | ||||||
| chr14:69898132
|
G | C | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+18355G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898132 | ||||||
| chr14:69898150
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0044 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.99+18373C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898150 | ||||||
| chr14:69898163
|
T | C | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+18386T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898163 | ||||||
| chr14:69898176
|
G | T | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.99+18399G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898176 | ||||||
| chr14:69898284
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.99+18507A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898284 | ||||||
| chr14:69898464
|
G | GT | 22 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(19): Show | 23 | HG00733.hp2 HG01069.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+18697dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69898464 | |||||
| chr14:69898479
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.99+18702T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898479 | ||||||
| chr14:69898519
|
G | A | 6 | a0001c0001t0001g0222a0001c0001t0005g0221a0001c0001t0006g0080others(3): Show | 6 | HG00738.hp1 HG01123.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+18742G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898519 | ||||||
| chr14:69898619
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.99+18842C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898619 | ||||||
| chr14:69898624
|
G | A | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+18847G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898624 | ||||||
| chr14:69898763
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0005g0221 | 2 | HG00738.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.99+18986A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898763 | ||||||
| chr14:69898882
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.99+19105C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898882 | ||||||
| chr14:69898918
|
T | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(12): Show | 15 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+19141T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898918 | ||||||
| chr14:69898940
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+19163G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69898940 | ||||||
| chr14:69899007
|
G | C | 1 | a0001c0002t0002g0012 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.99+19230G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899007 | ||||||
| chr14:69899020
|
G | A | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+19243G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899020 | ||||||
| chr14:69899207
|
A | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.99+19430A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899207 | ||||||
| chr14:69899287
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0006g0109 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.99+19510C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899287 | ||||||
| chr14:69899328
|
A | G | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+19551A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899328 | ||||||
| chr14:69899343
|
A | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+19566A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899343 | ||||||
| chr14:69899379
|
C | T | 1 | a0001c0001t0008g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+19602C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899379 | ||||||
| chr14:69899493
|
C | T | 1 | a0001c0003t0002g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.99+19716C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899493 | ||||||
| chr14:69899550
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+19773G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899550 | ||||||
| chr14:69899660
|
T | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+19883T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899660 | ||||||
| chr14:69899692
|
C | T | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.99+19915C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899692 | ||||||
| chr14:69899720
|
A | G | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+19943A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899720 | ||||||
| chr14:69899742
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+19965C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899742 | ||||||
| chr14:69899749
|
T | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(10): Show | 13 | HG02970.hp2 NA18940.hp2 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+19972T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899749 | ||||||
| chr14:69899886
|
C | G | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+20109C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899886 | ||||||
| chr14:69899967
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+20190G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899967 | ||||||
| chr14:69899988
|
T | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.99+20211T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69899988 | ||||||
| chr14:69900157
|
A | G | 43 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0050others(40): Show | 45 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+20380A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900157 | ||||||
| chr14:69900176
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0135a0001c0002t0002g0136 | 3 | NA19003.hp1 NA19005.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.99+20399G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900176 | ||||||
| chr14:69900179
|
G | C | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+20402G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900179 | ||||||
| chr14:69900237
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99+20460C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900237 | ||||||
| chr14:69900238
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99+20461C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900238 | ||||||
| chr14:69900273
|
G | T | 1 | a0001c0001t0032g0170 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.99+20496G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900273 | ||||||
| chr14:69900355
|
G | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.99+20578G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900355 | ||||||
| chr14:69900413
|
A | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+20636A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900413 | ||||||
| chr14:69900468
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.99+20691G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900468 | ||||||
| chr14:69900472
|
A | G | 38 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+20695A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900472 | ||||||
| chr14:69900485
|
C | G | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+20708C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900485 | ||||||
| chr14:69900523
|
G | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+20746G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900523 | ||||||
| chr14:69900792
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(16): Show | 19 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+21015G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69900792 | ||||||
| chr14:69901313
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+21536T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901313 | ||||||
| chr14:69901371
|
A | C | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+21594A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901371 | ||||||
| chr14:69901620
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+21843G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901620 | ||||||
| chr14:69901815
|
T | C | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+22038T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901815 | ||||||
| chr14:69901823
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+22046G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901823 | ||||||
| chr14:69901960
|
G | T | 23 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0050others(20): Show | 24 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+22183G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901960 | ||||||
| chr14:69901984
|
C | T | 23 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0050others(20): Show | 24 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+22207C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69901984 | ||||||
| chr14:69902332
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+22555C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902332 | ||||||
| chr14:69902349
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.99+22572G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902349 | ||||||
| chr14:69902370
|
C | T | 1 | a0001c0001t0016g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+22593C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902370 | ||||||
| chr14:69902651
|
C | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+22874C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902651 | ||||||
| chr14:69902665
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99+22888G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902665 | ||||||
| chr14:69902669
|
C | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+22892C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902669 | ||||||
| chr14:69902669
|
C | T | 13 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0091others(10): Show | 14 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+22892C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902669 | ||||||
| chr14:69902688
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0014g0173 | 2 | HG00639.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.99+22911C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902688 | ||||||
| chr14:69902742
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0007g0095 | 3 | HG02622.hp1 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.99+22965G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902742 | ||||||
| chr14:69902742
|
G | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+22965G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902742 | ||||||
| chr14:69902761
|
C | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0091others(11): Show | 15 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+22984C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902761 | ||||||
| chr14:69902766
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+22989G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902766 | ||||||
| chr14:69902769
|
G | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+22992G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902769 | ||||||
| chr14:69902783
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+23006G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902783 | ||||||
| chr14:69902808
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+23031C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902808 | ||||||
| chr14:69902851
|
T | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.99+23074T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902851 | ||||||
| chr14:69902900
|
G | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0091others(7): Show | 11 | HG00642.hp2 HG01099.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+23123G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902900 | ||||||
| chr14:69902963
|
C | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+23186C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69902963 | ||||||
| chr14:69903036
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+23259C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903036 | ||||||
| chr14:69903038
|
A | AC | 4 | a0001c0001t0001g0237a0001c0001t0003g0259a0001c0002t0002g0151others(1): Show | 4 | HG01175.hp1 NA18940.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+23265dupC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69903038 | |||||
| chr14:69903120
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.99+23343T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903120 | ||||||
| chr14:69903208
|
T | A | 1 | a0001c0001t0003g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.99+23431T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903208 | ||||||
| chr14:69903208
|
T | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0119others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+23431T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903208 | ||||||
| chr14:69903234
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.99+23457C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903234 | ||||||
| chr14:69903244
|
G | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+23467G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903244 | ||||||
| chr14:69903266
|
C | T | 13 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0108others(10): Show | 14 | HG00738.hp2 HG01069.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+23489C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903266 | ||||||
| chr14:69903292
|
C | T | 57 | a0001c0001t0001g0018a0001c0001t0001g0119a0001c0001t0001g0121others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+23515C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903292 | ||||||
| chr14:69903321
|
C | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.99+23544C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903321 | ||||||
| chr14:69903374
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+23597C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903374 | ||||||
| chr14:69903379
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(16): Show | 19 | HG00733.hp2 HG02257.hp1 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+23602C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903379 | ||||||
| chr14:69903380
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+23603G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903380 | ||||||
| chr14:69903387
|
A | AC | 4 | a0001c0001t0001g0048a0001c0001t0001g0155a0001c0001t0004g0013others(1): Show | 4 | HG00741.hp1 HG01243.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+23614dupC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69903387 | |||||
| chr14:69903454
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(15): Show | 18 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+23677G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903454 | ||||||
| chr14:69903485
|
T | C | 1 | a0001c0001t0003g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.99+23708T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903485 | ||||||
| chr14:69903593
|
A | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(15): Show | 18 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+23816A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903593 | ||||||
| chr14:69903594
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(16): Show | 19 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+23817C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903594 | ||||||
| chr14:69903612
|
G | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(15): Show | 18 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+23835G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903612 | ||||||
| chr14:69903664
|
C | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+23887C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903664 | ||||||
| chr14:69903704
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+23927G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903704 | ||||||
| chr14:69903709
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0020g0096 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.99+23932C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903709 | ||||||
| chr14:69903828
|
T | G | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.99+24051T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903828 | ||||||
| chr14:69903863
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.99+24086A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903863 | ||||||
| chr14:69903900
|
T | TA | 15 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0050others(12): Show | 15 | HG01074.hp2 HG01106.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+24139dupA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69903900 | |||||
| chr14:69903900
|
TA | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.99+24139delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69903900 | |||||
| chr14:69903941
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+24164G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69903941 | ||||||
| chr14:69904014
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0110others(9): Show | 13 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+24237C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904014 | ||||||
| chr14:69904468
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.99+24691G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904468 | ||||||
| chr14:69904485
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+24708A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904485 | ||||||
| chr14:69904690
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0006g0109 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.99+24913C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904690 | ||||||
| chr14:69904743
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0235 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.99+24966A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904743 | ||||||
| chr14:69904744
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0111others(7): Show | 11 | HG01168.hp1 HG01257.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+24967T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904744 | ||||||
| chr14:69904922
|
T | C | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.99+25145T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904922 | ||||||
| chr14:69904986
|
G | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+25209G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69904986 | ||||||
| chr14:69905036
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.99+25259A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905036 | ||||||
| chr14:69905124
|
T | C | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.99+25347T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905124 | ||||||
| chr14:69905210
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+25433G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905210 | ||||||
| chr14:69905224
|
G | A | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+25447G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905224 | ||||||
| chr14:69905304
|
G | A | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+25527G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905304 | ||||||
| chr14:69905423
|
C | T | 1 | a0001c0002t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.99+25646C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905423 | ||||||
| chr14:69905444
|
C | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(30): Show | 34 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.99+25667C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905444 | ||||||
| chr14:69905444
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.99+25667C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905444 | ||||||
| chr14:69905449
|
A | G | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+25672A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905449 | ||||||
| chr14:69905757
|
A | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99+25980A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905757 | ||||||
| chr14:69905767
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99+25990G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905767 | ||||||
| chr14:69905973
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+26196G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69905973 | ||||||
| chr14:69906190
|
G | C | 33 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0076others(30): Show | 35 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.99+26413G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906190 | ||||||
| chr14:69906396
|
G | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.99+26619G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906396 | ||||||
| chr14:69906409
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.99+26632C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906409 | ||||||
| chr14:69906482
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+26705C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906482 | ||||||
| chr14:69906491
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+26714G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906491 | ||||||
| chr14:69906504
|
T | A | 1 | a0001c0005t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+26727T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906504 | ||||||
| chr14:69906590
|
A | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0020others(104): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.99+26813A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906590 | ||||||
| chr14:69906837
|
A | C | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+27060A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906837 | ||||||
| chr14:69906874
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0007g0102a0001c0001t0027g0036 | 3 | HG02922.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.99+27097G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69906874 | ||||||
| chr14:69907114
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+27337G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907114 | ||||||
| chr14:69907141
|
G | T | 3 | a0001c0001t0001g0143a0001c0001t0002g0135a0001c0002t0002g0136 | 3 | NA19003.hp1 NA19005.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.99+27364G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907141 | ||||||
| chr14:69907150
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+27373C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907150 | ||||||
| chr14:69907405
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.99+27628G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907405 | ||||||
| chr14:69907420
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.99+27643T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907420 | ||||||
| chr14:69907638
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.99+27861A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69907638 | ||||||
| chr14:69908150
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.99+28373G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908150 | ||||||
| chr14:69908192
|
G | GACCCATT others(6): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0125 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.99+28415_99+28416i others(15): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908192 | ||||||
| chr14:69908224
|
C | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.99+28447C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908224 | ||||||
| chr14:69908533
|
A | G | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+28756A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908533 | ||||||
| chr14:69908560
|
A | G | 1 | a0001c0002t0002g0248 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.99+28783A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908560 | ||||||
| chr14:69908660
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0003g0056 | 3 | HG02809.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99+28883G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908660 | ||||||
| chr14:69908844
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0235 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.99+29067C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908844 | ||||||
| chr14:69908909
|
G | A | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.99+29132G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69908909 | ||||||
| chr14:69909309
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG01074.hp2 HG02145.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+29532A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909309 | ||||||
| chr14:69909348
|
G | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0091others(10): Show | 14 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+29571G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909348 | ||||||
| chr14:69909518
|
A | G | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.99+29741A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909518 | ||||||
| chr14:69909652
|
T | C | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.99+29875T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909652 | ||||||
| chr14:69909814
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(15): Show | 18 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+30037C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909814 | ||||||
| chr14:69909815
|
G | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+30038G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909815 | ||||||
| chr14:69909822
|
G | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.99+30045G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909822 | ||||||
| chr14:69909843
|
A | G | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+30066A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909843 | ||||||
| chr14:69909887
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99+30110C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909887 | ||||||
| chr14:69909957
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.99+30180G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909957 | ||||||
| chr14:69909995
|
A | G | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.99+30218A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69909995 | ||||||
| chr14:69910133
|
T | C | 29 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0065others(26): Show | 29 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+30356T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910133 | ||||||
| chr14:69910213
|
C | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0264others(4): Show | 8 | HG00738.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+30436C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910213 | ||||||
| chr14:69910245
|
C | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+30468C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910245 | ||||||
| chr14:69910262
|
A | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0114others(31): Show | 35 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+30485A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910262 | ||||||
| chr14:69910375
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+30598G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910375 | ||||||
| chr14:69910423
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.99+30646A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910423 | ||||||
| chr14:69910470
|
T | C | 1 | a0001c0001t0007g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+30693T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910470 | ||||||
| chr14:69910598
|
A | AT | 10 | a0001c0001t0001g0083a0001c0001t0001g0222a0001c0001t0005g0189others(7): Show | 10 | HG00738.hp1 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+30834dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69910598 | |||||
| chr14:69910598
|
AT | A | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.99+30834delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69910598 | |||||
| chr14:69910702
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0111others(7): Show | 11 | HG01168.hp1 HG01257.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+30925G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910702 | ||||||
| chr14:69910833
|
C | T | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.99+31056C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910833 | ||||||
| chr14:69910950
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.99+31173G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69910950 | ||||||
| chr14:69911074
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.99+31297T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69911074 | ||||||
| chr14:69911275
|
G | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+31498G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69911275 | ||||||
| chr14:69911482
|
G | C | 236 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.99+31705G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69911482 | ||||||
| chr14:69911972
|
C | T | 10 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0071others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+32195C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69911972 | ||||||
| chr14:69912341
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+32564C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912341 | ||||||
| chr14:69912425
|
T | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+32648T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912425 | ||||||
| chr14:69912488
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+32711G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912488 | ||||||
| chr14:69912498
|
C | G | 25 | a0001c0001t0001g0046a0001c0001t0001g0076a0001c0001t0001g0079others(22): Show | 27 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.99+32721C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912498 | ||||||
| chr14:69912713
|
A | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(15): Show | 18 | HG00733.hp2 HG02257.hp1 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+32936A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912713 | ||||||
| chr14:69912806
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.99+33029C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912806 | ||||||
| chr14:69912996
|
A | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.99+33219A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69912996 | ||||||
| chr14:69913065
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0060others(2): Show | 5 | HG00733.hp1 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+33288C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913065 | ||||||
| chr14:69913102
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02074.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+33325G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913102 | ||||||
| chr14:69913146
|
T | C | 9 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+33369T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913146 | ||||||
| chr14:69913344
|
A | G | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+33567A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913344 | ||||||
| chr14:69913353
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0018others(113): Show | 117 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.99+33576G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913353 | ||||||
| chr14:69913455
|
C | CGT | 41 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0076others(38): Show | 44 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.99+33694_99+33695d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69913455 | |||||
| chr14:69913455
|
C | CGTGT | 3 | a0001c0001t0005g0219a0001c0006t0001g0220a0001c0006t0001g0233 | 3 | HG00642.hp2 HG01099.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+33692_99+33695d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69913455 | |||||
| chr14:69913474
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99+33697G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913474 | ||||||
| chr14:69913524
|
T | C | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.99+33747T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913524 | ||||||
| chr14:69913802
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.99+34025A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913802 | ||||||
| chr14:69913947
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99+34170G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913947 | ||||||
| chr14:69913994
|
A | G | 56 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 57 | HG00642.hp2 HG00733.hp2 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+34217A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69913994 | ||||||
| chr14:69914169
|
C | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0008g0057others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+34392C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914169 | ||||||
| chr14:69914172
|
G | C | 1 | a0001c0002t0002g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.99+34395G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914172 | ||||||
| chr14:69914356
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 29 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+34579G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914356 | ||||||
| chr14:69914577
|
G | GAAAC | 87 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0041others(84): Show | 89 | HG00438.hp1 HG00558.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.99+34826_99+34829d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914577 | |||||
| chr14:69914655
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 29 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+34878C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914655 | ||||||
| chr14:69914865
|
T | TATTC | 37 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0031others(34): Show | 38 | HG00741.hp2 HG01069.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.99+35121_99+35124d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914865 | |||||
| chr14:69914865
|
T | TATTCATT others(1): Show |
28 | a0001c0001t0001g0044a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG00558.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.99+35117_99+35124d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914865 | |||||
| chr14:69914865
|
T | TATTCATT others(5): Show |
41 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0048others(38): Show | 42 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.99+35113_99+35124d others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914865 | |||||
| chr14:69914865
|
T | TATTCATT others(9): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0226others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+35109_99+35124d others(18): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914865 | |||||
| chr14:69914865
|
TATTC | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0055a0001c0001t0001g0073others(10): Show | 13 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+35121_99+35124d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69914865 | |||||
| chr14:69914941
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0229others(7): Show | 10 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+35164G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914941 | ||||||
| chr14:69914953
|
G | A | 13 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0085others(10): Show | 14 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+35176G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69914953 | ||||||
| chr14:69915113
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+35336C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915113 | ||||||
| chr14:69915219
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.99+35442A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915219 | ||||||
| chr14:69915285
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0002g0135a0001c0002t0002g0136 | 3 | NA19003.hp1 NA19005.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.99+35508A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915285 | ||||||
| chr14:69915363
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+35586C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915363 | ||||||
| chr14:69915501
|
T | C | 11 | a0001c0001t0001g0055a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+35724T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915501 | ||||||
| chr14:69915525
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.99+35748A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915525 | ||||||
| chr14:69915670
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.99+35893C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915670 | ||||||
| chr14:69915955
|
T | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(126): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.99+36178T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69915955 | ||||||
| chr14:69916072
|
G | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0084a0001c0001t0001g0085others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-36066G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916072 | ||||||
| chr14:69916193
|
C | T | 1 | a0001c0001t0005g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-35945C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916193 | ||||||
| chr14:69916300
|
C | T | 53 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0051others(50): Show | 53 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-35838C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916300 | ||||||
| chr14:69916365
|
G | A | 11 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0143others(8): Show | 12 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-35773G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916365 | ||||||
| chr14:69916437
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-35701G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916437 | ||||||
| chr14:69916586
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0229others(7): Show | 10 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-35552G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916586 | ||||||
| chr14:69916603
|
G | T | 53 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0051others(50): Show | 53 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-35535G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916603 | ||||||
| chr14:69916605
|
C | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0050others(73): Show | 77 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.100-35533C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916605 | ||||||
| chr14:69916711
|
A | G | 3 | a0001c0001t0001g0258a0001c0002t0002g0194a0001c0002t0024g0133 | 3 | HG00597.hp2 NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.100-35427A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916711 | ||||||
| chr14:69916732
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0143others(8): Show | 12 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-35406C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916732 | ||||||
| chr14:69916839
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100-35299C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916839 | ||||||
| chr14:69916968
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-35170A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916968 | ||||||
| chr14:69916991
|
A | G | 1 | a0001c0001t0030g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.100-35147A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69916991 | ||||||
| chr14:69917172
|
A | G | 1 | a0001c0002t0024g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.100-34966A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917172 | ||||||
| chr14:69917174
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0049others(31): Show | 35 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-34964T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917174 | ||||||
| chr14:69917414
|
T | C | 1 | a0001c0001t0011g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-34724T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917414 | ||||||
| chr14:69917499
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-34639C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917499 | ||||||
| chr14:69917535
|
G | A | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-34603G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917535 | ||||||
| chr14:69917660
|
T | C | 1 | a0001c0004t0004g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100-34478T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917660 | ||||||
| chr14:69917690
|
C | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0229others(7): Show | 10 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-34448C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917690 | ||||||
| chr14:69917703
|
C | T | 55 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0051others(52): Show | 55 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.100-34435C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917703 | ||||||
| chr14:69917735
|
A | G | 8 | a0001c0001t0001g0125a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-34403A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917735 | ||||||
| chr14:69917743
|
A | G | 42 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0051others(39): Show | 42 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.100-34395A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917743 | ||||||
| chr14:69917815
|
G | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0008g0057others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-34323G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917815 | ||||||
| chr14:69917869
|
T | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0229others(7): Show | 10 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-34269T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917869 | ||||||
| chr14:69917929
|
A | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0048others(32): Show | 36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-34209A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69917929 | ||||||
| chr14:69918023
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-34115A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918023 | ||||||
| chr14:69918232
|
A | AT | 27 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0063others(24): Show | 28 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-33905dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69918232 | |||||
| chr14:69918234
|
A | AT | 17 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 17 | HG01106.hp2 HG01109.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-33903dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69918234 | |||||
| chr14:69918234
|
A | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0028others(49): Show | 53 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.100-33904A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918234 | ||||||
| chr14:69918236
|
A | AT | 23 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0113others(20): Show | 24 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-33892dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69918236 | |||||
| chr14:69918236
|
A | T | 122 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0025others(119): Show | 124 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.100-33902A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918236 | ||||||
| chr14:69918238
|
T | A | 2 | a0001c0001t0001g0111a0001c0001t0021g0122 | 2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.100-33900T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918238 | ||||||
| chr14:69918241
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0112 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.100-33897T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918241 | ||||||
| chr14:69918252
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-33886A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918252 | ||||||
| chr14:69918297
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.100-33841C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918297 | ||||||
| chr14:69918442
|
G | T | 1 | a0001c0002t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100-33696G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918442 | ||||||
| chr14:69918489
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0049others(31): Show | 35 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-33649A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918489 | ||||||
| chr14:69918491
|
G | A | 2 | a0001c0001t0004g0019a0002c0013t0023g0027 | 2 | HG02280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.100-33647G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918491 | ||||||
| chr14:69918519
|
C | T | 1 | a0001c0001t0005g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-33619C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918519 | ||||||
| chr14:69918523
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-33615C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918523 | ||||||
| chr14:69918654
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-33484T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918654 | ||||||
| chr14:69918663
|
T | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0065others(8): Show | 11 | HG01081.hp1 HG01175.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-33475T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918663 | ||||||
| chr14:69918719
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-33419A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918719 | ||||||
| chr14:69918841
|
C | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0229others(7): Show | 10 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-33297C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918841 | ||||||
| chr14:69918894
|
T | C | 38 | a0001c0001t0001g0025a0001c0001t0001g0082a0001c0001t0001g0098others(35): Show | 38 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-33244T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918894 | ||||||
| chr14:69918904
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-33234G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918904 | ||||||
| chr14:69918990
|
G | T | 7 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | HG01167.hp1 HG01175.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-33148G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69918990 | ||||||
| chr14:69919063
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100-33075C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919063 | ||||||
| chr14:69919114
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-33024G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919114 | ||||||
| chr14:69919150
|
G | T | 1 | a0001c0002t0002g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-32988G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919150 | ||||||
| chr14:69919201
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-32937C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919201 | ||||||
| chr14:69919218
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100-32920A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919218 | ||||||
| chr14:69919219
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100-32919A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919219 | ||||||
| chr14:69919274
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0111others(6): Show | 10 | HG01168.hp1 HG01257.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-32864C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919274 | ||||||
| chr14:69919686
|
T | G | 18 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-32452T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919686 | ||||||
| chr14:69919705
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-32433G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919705 | ||||||
| chr14:69919783
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0111a0001c0001t0001g0123others(5): Show | 8 | HG01168.hp1 HG01257.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-32355C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919783 | ||||||
| chr14:69919852
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0143others(8): Show | 12 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-32286A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919852 | ||||||
| chr14:69919859
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.100-32279A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919859 | ||||||
| chr14:69919898
|
A | G | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-32240A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919898 | ||||||
| chr14:69919908
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100-32230A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919908 | ||||||
| chr14:69919910
|
A | AC | 24 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0065others(21): Show | 24 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.100-32216dupC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69919910 | |||||
| chr14:69919910
|
AC | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0022others(77): Show | 83 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-32216delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69919910 | |||||
| chr14:69919912
|
C | CG | 15 | a0001c0001t0001g0055a0001c0001t0001g0073a0001c0001t0001g0084others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-32226_100-3222 others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919912 | ||||||
| chr14:69919917
|
C | A | 2 | a0001c0001t0001g0222a0001c0006t0034g0092 | 2 | HG00738.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.100-32221C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919917 | ||||||
| chr14:69919920
|
C | T | 2 | a0001c0001t0004g0013a0001c0001t0004g0177 | 2 | NA18989.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.100-32218C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69919920 | ||||||
| chr14:69920026
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0264others(5): Show | 9 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-32112T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920026 | ||||||
| chr14:69920348
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-31790G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920348 | ||||||
| chr14:69920408
|
CAT | C | 3 | a0001c0001t0001g0108a0001c0001t0002g0003a0004c0012t0001g0107 | 4 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-31727_100-3172 others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69920408 | |||||
| chr14:69920448
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-31690G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920448 | ||||||
| chr14:69920456
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.100-31682A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920456 | ||||||
| chr14:69920517
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0027g0036others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-31621A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920517 | ||||||
| chr14:69920570
|
A | G | 1 | a0001c0001t0003g0016 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.100-31568A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920570 | ||||||
| chr14:69920659
|
A | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0017others(90): Show | 94 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.100-31479A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920659 | ||||||
| chr14:69920737
|
T | C | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-31401T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920737 | ||||||
| chr14:69920839
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0022g0094 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-31299G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920839 | ||||||
| chr14:69920919
|
C | G | 3 | a0001c0001t0001g0073a0001c0001t0007g0095a0001c0001t0026g0072 | 3 | HG02486.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.100-31219C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69920919 | ||||||
| chr14:69921042
|
C | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-31096C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921042 | ||||||
| chr14:69921125
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-31013C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921125 | ||||||
| chr14:69921187
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0005g0239 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.100-30951G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921187 | ||||||
| chr14:69921338
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0206a0001c0001t0001g0217others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-30800C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921338 | ||||||
| chr14:69921353
|
G | C | 1 | a0001c0002t0002g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-30785G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921353 | ||||||
| chr14:69921400
|
C | T | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-30738C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921400 | ||||||
| chr14:69921436
|
C | T | 1 | a0001c0001t0007g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-30702C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921436 | ||||||
| chr14:69921462
|
A | C | 1 | a0001c0001t0003g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100-30676A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921462 | ||||||
| chr14:69921651
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0027g0036a0002c0013t0023g0027 | 3 | HG02280.hp2 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.100-30487C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921651 | ||||||
| chr14:69921846
|
C | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0084others(9): Show | 13 | HG02109.hp1 HG02647.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-30292C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921846 | ||||||
| chr14:69921895
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30243C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921895 | ||||||
| chr14:69921897
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.100-30241T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69921897 | ||||||
| chr14:69922282
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.100-29856C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922282 | ||||||
| chr14:69922283
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0113a0001c0001t0001g0114others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-29855G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922283 | ||||||
| chr14:69922393
|
G | C | 67 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0029others(64): Show | 67 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.100-29745G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922393 | ||||||
| chr14:69922570
|
A | T | 4 | a0001c0005t0001g0033a0001c0005t0001g0040a0001c0005t0001g0069others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-29568A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922570 | ||||||
| chr14:69922572
|
T | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(173): Show | 181 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.100-29566T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922572 | ||||||
| chr14:69922583
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-29555G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922583 | ||||||
| chr14:69922932
|
C | CT | 30 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0048others(27): Show | 30 | HG00280.hp1 HG00639.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.100-29198dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69922932 | |||||
| chr14:69922932
|
C | CTT | 11 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0188others(8): Show | 12 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-29199_100-2919 others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69922932 | |||||
| chr14:69922941
|
G | GT | 4 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-29189dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69922941 | |||||
| chr14:69922941
|
G | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(79): Show | 84 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.100-29197G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69922941 | ||||||
| chr14:69923136
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-29002G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923136 | ||||||
| chr14:69923153
|
G | A | 39 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0048others(36): Show | 40 | HG00280.hp1 HG00639.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.100-28985G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923153 | ||||||
| chr14:69923187
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100-28951C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923187 | ||||||
| chr14:69923234
|
T | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(175): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.100-28904T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923234 | ||||||
| chr14:69923241
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-28897G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923241 | ||||||
| chr14:69923428
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.100-28710G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923428 | ||||||
| chr14:69923537
|
A | G | 7 | a0001c0001t0001g0049a0001c0001t0001g0188a0001c0001t0001g0192others(4): Show | 8 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-28601A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923537 | ||||||
| chr14:69923690
|
C | G | 243 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(240): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-28448C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923690 | ||||||
| chr14:69923813
|
G | T | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-28325G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923813 | ||||||
| chr14:69923830
|
T | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-28308T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69923830 | ||||||
| chr14:69924039
|
C | T | 243 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(240): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-28099C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924039 | ||||||
| chr14:69924396
|
C | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0113others(7): Show | 10 | HG00280.hp1 HG00639.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-27742C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924396 | ||||||
| chr14:69924401
|
C | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.100-27737C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924401 | ||||||
| chr14:69924434
|
AC | A | 15 | a0001c0001t0001g0079a0001c0001t0001g0126a0001c0001t0001g0127others(12): Show | 15 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-27703delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924434 | ||||||
| chr14:69924555
|
T | C | 12 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-27583T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924555 | ||||||
| chr14:69924681
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0032g0170 | 4 | HG01433.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27457G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924681 | ||||||
| chr14:69924695
|
AGGGAGCT others(171): Show |
A | 11 | a0001c0001t0001g0140a0001c0001t0003g0088a0001c0001t0006g0210others(8): Show | 11 | HG00323.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-27357_100-2718 others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924695 | |||||
| chr14:69924725
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(1): Show | 4 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27413G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924725 | ||||||
| chr14:69924744
|
AGTAGGGG others(20): Show |
A | 102 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0029others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-27357_100-2733 others(31): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924744 | |||||
| chr14:69924757
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27381A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924757 | ||||||
| chr14:69924759
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27379G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924759 | ||||||
| chr14:69924759
|
GGAGGTAG others(64): Show |
G | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.100-27357_100-2728 others(75): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924759 | |||||
| chr14:69924771
|
G | GGTAGGGG others(117): Show |
1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-27358_100-2735 others(128): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924771 | |||||
| chr14:69924771
|
G | GGTAGGGG others(224): Show |
1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100-27358_100-2735 others(235): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924771 | |||||
| chr14:69924771
|
G | GGTAGGGG others(545): Show |
1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27358_100-2735 others(556): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924771 | |||||
| chr14:69924771
|
GGTAGGGG others(144): Show |
G | 1 | a0001c0001t0005g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-27318_100-2716 others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924771 | |||||
| chr14:69924774
|
AGGGGAGG others(21): Show |
A | 28 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 28 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-27360_100-2733 others(32): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924774 | |||||
| chr14:69924777
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27361G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924777 | ||||||
| chr14:69924781
|
G | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0160a0001c0003t0002g0171others(1): Show | 4 | HG01069.hp2 HG01346.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27357G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924781 | ||||||
| chr14:69924784
|
A | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0001g0160others(2): Show | 5 | HG01069.hp2 HG01346.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27354A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924784 | ||||||
| chr14:69924789
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27349G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924789 | ||||||
| chr14:69924791
|
T | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0160a0001c0003t0002g0171others(1): Show | 4 | HG01069.hp2 HG01346.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27347T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924791 | ||||||
| chr14:69924799
|
G | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0160a0001c0003t0002g0171others(1): Show | 4 | HG01069.hp2 HG01346.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27339G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924799 | ||||||
| chr14:69924802
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27336G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924802 | ||||||
| chr14:69924804
|
GGAGCTAG others(19): Show |
G | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-27330_100-2730 others(30): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924804 | |||||
| chr14:69924816
|
G | GGCAGGGG others(55): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27321_100-2732 others(66): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924816 | |||||
| chr14:69924820
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01069.hp2 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-27318A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924820 | ||||||
| chr14:69924821
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01069.hp2 HG01074.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-27317A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924821 | ||||||
| chr14:69924822
|
G | A | 2 | a0001c0001t0001g0108a0004c0012t0001g0107 | 2 | HG01069.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.100-27316G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924822 | ||||||
| chr14:69924826
|
G | GT | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27312_100-2731 others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924826 | ||||||
| chr14:69924826
|
G | GTAGGGGA others(29): Show |
2 | a0001c0001t0001g0108a0004c0012t0001g0107 | 2 | HG01069.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.100-27312_100-2731 others(40): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924826 | ||||||
| chr14:69924828
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01069.hp2 HG01074.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-27310G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924828 | ||||||
| chr14:69924830
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01069.hp2 HG01074.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-27308A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924830 | ||||||
| chr14:69924848
|
G | A | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27290G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924848 | ||||||
| chr14:69924852
|
C | G | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27286C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924852 | ||||||
| chr14:69924860
|
G | A | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27278G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924860 | ||||||
| chr14:69924862
|
C | T | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27276C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924862 | ||||||
| chr14:69924870
|
C | G | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27268C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924870 | ||||||
| chr14:69924873
|
G | A | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27265G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924873 | ||||||
| chr14:69924879
|
C | G | 2 | a0001c0001t0001g0160a0001c0003t0002g0171 | 2 | NA18940.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.100-27259C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924879 | ||||||
| chr14:69924889
|
TAGGAGAG others(10): Show |
T | 11 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(8): Show | 11 | HG01175.hp2 HG01243.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-27233_100-2721 others(21): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924889 | |||||
| chr14:69924906
|
G | GT | 4 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-27232_100-2723 others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924906 | ||||||
| chr14:69924968
|
G | GCAGGGGA others(11): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27170_100-2716 others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924968 | ||||||
| chr14:69924969
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27169T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924969 | ||||||
| chr14:69924971
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-27167G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924971 | ||||||
| chr14:69924972
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG01074.hp2 HG02818.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27166A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924972 | ||||||
| chr14:69924977
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27161G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924977 | ||||||
| chr14:69924981
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27157A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924981 | ||||||
| chr14:69924985
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27153G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924985 | ||||||
| chr14:69924990
|
GGAGGTAG others(87): Show |
G | 61 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.100-27126_100-2703 others(98): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924990 | |||||
| chr14:69924993
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.100-27145G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924993 | ||||||
| chr14:69924999
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27139G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69924999 | ||||||
| chr14:69924999
|
GGAGGTAG others(78): Show |
G | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 190 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.100-27027_100-2694 others(89): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69924999 | |||||
| chr14:69925003
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0006g0230 | 2 | HG01517.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.100-27135G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925003 | ||||||
| chr14:69925006
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.100-27132G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925006 | ||||||
| chr14:69925011
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27127G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925011 | ||||||
| chr14:69925013
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0006g0230 | 2 | HG01517.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.100-27125T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925013 | ||||||
| chr14:69925017
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27121G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925017 | ||||||
| chr14:69925021
|
C | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-27117C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925021 | ||||||
| chr14:69925022
|
T | TAGGGGAG others(58): Show |
2 | a0001c0001t0001g0071a0001c0001t0006g0230 | 2 | HG01517.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.100-27116_100-2711 others(69): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925022 | ||||||
| chr14:69925023
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27115G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925023 | ||||||
| chr14:69925025
|
G | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(1): Show | 4 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-27113G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925025 | ||||||
| chr14:69925028
|
G | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27110G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925028 | ||||||
| chr14:69925031
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27107A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925031 | ||||||
| chr14:69925036
|
C | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27102C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925036 | ||||||
| chr14:69925040
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27098A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925040 | ||||||
| chr14:69925042
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(1): Show | 4 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-27096A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925042 | ||||||
| chr14:69925043
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27095A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925043 | ||||||
| chr14:69925044
|
G | GC | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(1): Show | 4 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-27094_100-2709 others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925044 | ||||||
| chr14:69925045
|
G | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27093G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925045 | ||||||
| chr14:69925057
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(2): Show | 5 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27081G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925057 | ||||||
| chr14:69925064
|
GT | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(2): Show | 5 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27073delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925064 | ||||||
| chr14:69925065
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27073T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925065 | ||||||
| chr14:69925066
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27072G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925066 | ||||||
| chr14:69925069
|
A | AG | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0071others(2): Show | 5 | HG01517.hp2 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-27068dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69925069 | |||||
| chr14:69925069
|
A | AGGAGGAG others(5): Show |
1 | a0001c0001t0001g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-27068_100-2706 others(16): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69925069 | |||||
| chr14:69925079
|
C | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27059C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925079 | ||||||
| chr14:69925084
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01074.hp2 HG01517.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27054A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925084 | ||||||
| chr14:69925133
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-27005G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925133 | ||||||
| chr14:69925177
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(75): Show | 81 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.100-26961G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925177 | ||||||
| chr14:69925224
|
C | G | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(99): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.100-26914C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925224 | ||||||
| chr14:69925380
|
T | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(63): Show | 69 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.100-26758T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925380 | ||||||
| chr14:69925451
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0005g0189 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.100-26687C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925451 | ||||||
| chr14:69925454
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.100-26684A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925454 | ||||||
| chr14:69925457
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0188a0001c0001t0001g0192 | 3 | HG02922.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.100-26681G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925457 | ||||||
| chr14:69925560
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-26578G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925560 | ||||||
| chr14:69925575
|
T | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.100-26563T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925575 | ||||||
| chr14:69925628
|
G | A | 1 | a0001c0002t0002g0012 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.100-26510G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925628 | ||||||
| chr14:69925634
|
G | A | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0083others(8): Show | 12 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-26504G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925634 | ||||||
| chr14:69925640
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-26498G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925640 | ||||||
| chr14:69925847
|
G | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(32): Show | 35 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-26291G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925847 | ||||||
| chr14:69925859
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-26279A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925859 | ||||||
| chr14:69925989
|
G | C | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(2): Show | 5 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-26149G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925989 | ||||||
| chr14:69925997
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-26141C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69925997 | ||||||
| chr14:69926018
|
G | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-26120G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926018 | ||||||
| chr14:69926047
|
A | AT | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.100-26079dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69926047 | |||||
| chr14:69926047
|
AT | A | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0084others(7): Show | 11 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-26079delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69926047 | |||||
| chr14:69926189
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-25949A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926189 | ||||||
| chr14:69926328
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 96 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-25810T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926328 | ||||||
| chr14:69926387
|
T | G | 2 | a0001c0001t0001g0073a0001c0001t0026g0072 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.100-25751T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926387 | ||||||
| chr14:69926389
|
A | C | 2 | a0001c0001t0001g0074a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.100-25749A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926389 | ||||||
| chr14:69926407
|
T | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0076a0001c0001t0001g0128others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-25731T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926407 | ||||||
| chr14:69926461
|
T | C | 82 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0029others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-25677T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926461 | ||||||
| chr14:69926667
|
C | T | 1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.100-25471C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926667 | ||||||
| chr14:69926704
|
C | A | 3 | a0001c0001t0001g0098a0001c0001t0027g0036a0002c0013t0023g0027 | 3 | HG02280.hp2 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.100-25434C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926704 | ||||||
| chr14:69926818
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0118others(3): Show | 7 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-25320T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926818 | ||||||
| chr14:69926961
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-25177G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926961 | ||||||
| chr14:69926965
|
C | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(76): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-25173C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926965 | ||||||
| chr14:69926971
|
T | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(32): Show | 35 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-25167T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926971 | ||||||
| chr14:69926975
|
C | T | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-25163C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69926975 | ||||||
| chr14:69927046
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-25092A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927046 | ||||||
| chr14:69927067
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0001g0179a0001c0001t0001g0231others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-25071T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927067 | ||||||
| chr14:69927086
|
A | G | 1 | a0001c0002t0002g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.100-25052A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927086 | ||||||
| chr14:69927264
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0006g0109 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.100-24874A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927264 | ||||||
| chr14:69927422
|
T | A | 44 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0140others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.100-24716T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927422 | ||||||
| chr14:69927677
|
A | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-24461A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927677 | ||||||
| chr14:69927853
|
G | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0084others(7): Show | 11 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-24285G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927853 | ||||||
| chr14:69927956
|
G | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0008g0062 | 3 | HG02109.hp1 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100-24182G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69927956 | ||||||
| chr14:69928047
|
T | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0015g0054others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-24091T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928047 | ||||||
| chr14:69928078
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-24060C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928078 | ||||||
| chr14:69928091
|
C | G | 196 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.100-24047C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928091 | ||||||
| chr14:69928186
|
A | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(146): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-23952A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928186 | ||||||
| chr14:69928285
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100-23853C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928285 | ||||||
| chr14:69928287
|
G | C | 1 | a0001c0003t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-23851G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928287 | ||||||
| chr14:69928423
|
G | A | 1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.100-23715G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928423 | ||||||
| chr14:69928548
|
C | T | 10 | a0001c0001t0002g0181a0001c0001t0002g0207a0001c0001t0003g0198others(7): Show | 10 | HG00323.hp1 NA18949.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-23590C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928548 | ||||||
| chr14:69928583
|
G | T | 44 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0140others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.100-23555G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928583 | ||||||
| chr14:69928612
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0205others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-23526C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928612 | ||||||
| chr14:69928615
|
T | TG | 28 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 28 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-23513dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69928615 | |||||
| chr14:69928615
|
TG | T | 149 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(146): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-23513delG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69928615 | |||||
| chr14:69928617
|
G | T | 3 | a0001c0001t0001g0166a0001c0002t0002g0194a0001c0002t0024g0133 | 3 | HG00597.hp2 HG02004.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.100-23521G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928617 | ||||||
| chr14:69928618
|
G | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0063 | 3 | HG01496.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-23520G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928618 | ||||||
| chr14:69928618
|
G | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01106.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-23520G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928618 | ||||||
| chr14:69928619
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-23519G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928619 | ||||||
| chr14:69928619
|
G | C | 2 | a0001c0001t0013g0147a0001c0002t0002g0180 | 2 | HG02735.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.100-23519G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69928619 | ||||||
| chr14:69929010
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.100-23128G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929010 | ||||||
| chr14:69929013
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.100-23125C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929013 | ||||||
| chr14:69929038
|
C | G | 1 | a0001c0002t0002g0012 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.100-23100C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929038 | ||||||
| chr14:69929056
|
C | T | 1 | a0001c0003t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-23082C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929056 | ||||||
| chr14:69929081
|
A | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(5): Show | 8 | NA18940.hp2 NA18956.hp1 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-23057A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929081 | ||||||
| chr14:69929173
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-22965G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929173 | ||||||
| chr14:69929197
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100-22941G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929197 | ||||||
| chr14:69929222
|
T | G | 45 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.100-22916T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929222 | ||||||
| chr14:69929254
|
C | G | 1 | a0001c0001t0007g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-22884C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929254 | ||||||
| chr14:69929351
|
A | G | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0084others(7): Show | 11 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-22787A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929351 | ||||||
| chr14:69929455
|
C | T | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100-22683C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929455 | ||||||
| chr14:69929494
|
C | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(1): Show | 4 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22644C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929494 | ||||||
| chr14:69929534
|
C | T | 1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.100-22604C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929534 | ||||||
| chr14:69929714
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100-22424C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929714 | ||||||
| chr14:69929786
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.100-22352G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929786 | ||||||
| chr14:69929855
|
G | A | 44 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0140others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.100-22283G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929855 | ||||||
| chr14:69929857
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22281G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929857 | ||||||
| chr14:69929867
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.100-22271C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69929867 | ||||||
| chr14:69930030
|
G | T | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100-22108G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930030 | ||||||
| chr14:69930084
|
A | G | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-22054A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930084 | ||||||
| chr14:69930139
|
C | T | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100-21999C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930139 | ||||||
| chr14:69930164
|
T | G | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0017others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-21974T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930164 | ||||||
| chr14:69930167
|
A | ACCCCTGA others(16): Show |
8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(5): Show | 9 | HG01074.hp2 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-21952_100-2193 others(27): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(39): Show |
2 | a0001c0001t0009g0037a0001c0001t0009g0038 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.100-21930_100-2192 others(50): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(85): Show |
7 | a0001c0001t0001g0090a0001c0001t0002g0181a0001c0001t0003g0238others(4): Show | 7 | HG02647.hp2 NA18949.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-21930_100-2192 others(96): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(62): Show |
19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0068others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-21930_100-2192 others(73): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(108): Show |
2 | a0001c0001t0005g0221a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.100-21930_100-2192 others(119): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(39): Show |
3 | a0001c0001t0001g0031a0001c0001t0003g0088a0006c0010t0001g0035 | 3 | HG02257.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-21948_100-2190 others(50): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(62): Show |
1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-21903_100-2190 others(73): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(85): Show |
2 | a0001c0001t0005g0103a0001c0001t0005g0104 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.100-21903_100-2190 others(96): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(223): Show |
1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-21903_100-2190 others(234): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930167
|
A | ACCCCTGA others(62): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0076others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21907_100-2190 others(73): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930167 | |||||
| chr14:69930186
|
C | CCACTCCC others(16): Show |
3 | a0001c0001t0002g0158a0001c0002t0001g0137a0001c0002t0002g0180 | 3 | NA18950.hp2 NA18956.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.100-21948_100-2192 others(27): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930186 | |||||
| chr14:69930190
|
T | TCCCCTGA others(39): Show |
1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-21930_100-2192 others(50): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930190 | |||||
| chr14:69930190
|
T | TCCCCTGA others(16): Show |
1 | a0001c0001t0022g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-21929_100-2190 others(27): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930190 | |||||
| chr14:69930190
|
T | TCCCCTGA others(85): Show |
2 | a0001c0001t0001g0073a0001c0001t0026g0072 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.100-21903_100-2190 others(96): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930190 | |||||
| chr14:69930232
|
C | CCACTCCC others(62): Show |
1 | a0001c0001t0007g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.100-21903_100-2190 others(73): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69930232 | |||||
| chr14:69930232
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0027g0036a0002c0013t0023g0027 | 3 | HG02280.hp2 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.100-21906C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930232 | ||||||
| chr14:69930277
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0231 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.100-21861C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930277 | ||||||
| chr14:69930284
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0003c0009t0001g0045 | 3 | HG02109.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100-21854C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930284 | ||||||
| chr14:69930317
|
C | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(46): Show | 50 | HG00642.hp2 HG00733.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.100-21821C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930317 | ||||||
| chr14:69930321
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100-21817T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930321 | ||||||
| chr14:69930528
|
G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0008g0062 | 3 | HG02109.hp1 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100-21610G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930528 | ||||||
| chr14:69930699
|
G | A | 1 | a0002c0013t0023g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-21439G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930699 | ||||||
| chr14:69930715
|
G | A | 1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.100-21423G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930715 | ||||||
| chr14:69930760
|
G | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0058a0001c0001t0001g0087others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-21378G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930760 | ||||||
| chr14:69930798
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0015g0054others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-21340G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69930798 | ||||||
| chr14:69931026
|
T | C | 1 | a0001c0002t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.100-21112T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931026 | ||||||
| chr14:69931158
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-20980C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931158 | ||||||
| chr14:69931304
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-20834G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931304 | ||||||
| chr14:69931316
|
T | TC | 3 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0011g0075 | 3 | HG01175.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.100-20819dupC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69931316 | |||||
| chr14:69931329
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20809G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931329 | ||||||
| chr14:69931396
|
C | T | 1 | a0001c0002t0024g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.100-20742C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931396 | ||||||
| chr14:69931400
|
A | C | 16 | a0001c0001t0001g0049a0001c0001t0001g0083a0001c0001t0001g0098others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-20738A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931400 | ||||||
| chr14:69931401
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100-20737C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931401 | ||||||
| chr14:69931417
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0149a0001c0001t0013g0147others(1): Show | 4 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20721G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931417 | ||||||
| chr14:69931512
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20626T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69931512 | ||||||
| chr14:69932011
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20127T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932011 | ||||||
| chr14:69932021
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0015g0054others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-20117G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932021 | ||||||
| chr14:69932058
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20080C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932058 | ||||||
| chr14:69932070
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20068C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932070 | ||||||
| chr14:69932094
|
A | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20044A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932094 | ||||||
| chr14:69932103
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-20035T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932103 | ||||||
| chr14:69932175
|
G | A | 173 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(170): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.100-19963G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932175 | ||||||
| chr14:69932300
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0058others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-19838A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932300 | ||||||
| chr14:69932422
|
C | G | 1 | a0001c0005t0010g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100-19716C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932422 | ||||||
| chr14:69932503
|
G | A | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-19635G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932503 | ||||||
| chr14:69932584
|
G | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(166): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.100-19554G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932584 | ||||||
| chr14:69932597
|
C | T | 1 | a0001c0005t0010g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100-19541C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932597 | ||||||
| chr14:69932620
|
G | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0188a0001c0001t0001g0192others(2): Show | 6 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-19518G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932620 | ||||||
| chr14:69932743
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01106.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-19395C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932743 | ||||||
| chr14:69932788
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-19350C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932788 | ||||||
| chr14:69932962
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100-19176G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69932962 | ||||||
| chr14:69933090
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-19048C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933090 | ||||||
| chr14:69933097
|
G | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-19041G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933097 | ||||||
| chr14:69933127
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-19011G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933127 | ||||||
| chr14:69933184
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-18954A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933184 | ||||||
| chr14:69933365
|
C | CT | 69 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0020others(66): Show | 70 | HG00140.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.100-18764dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69933365 | |||||
| chr14:69933374
|
T | C | 1 | a0001c0002t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100-18764T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933374 | ||||||
| chr14:69933524
|
A | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0264a0001c0001t0002g0003others(3): Show | 7 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-18614A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933524 | ||||||
| chr14:69933599
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0011g0075 | 3 | HG01175.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.100-18539G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933599 | ||||||
| chr14:69933615
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01106.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-18523C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933615 | ||||||
| chr14:69933807
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0005g0189 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.100-18331C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933807 | ||||||
| chr14:69933916
|
T | C | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-18222T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933916 | ||||||
| chr14:69933968
|
T | A | 1 | a0001c0001t0016g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-18170T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933968 | ||||||
| chr14:69933973
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0007g0095others(1): Show | 4 | HG02486.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-18165T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69933973 | ||||||
| chr14:69934141
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-17997T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934141 | ||||||
| chr14:69934175
|
C | G | 29 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0055others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-17963C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934175 | ||||||
| chr14:69934196
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-17942A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934196 | ||||||
| chr14:69934224
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0188a0001c0001t0001g0192others(2): Show | 6 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-17914C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934224 | ||||||
| chr14:69934238
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-17900G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934238 | ||||||
| chr14:69934426
|
A | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0026others(91): Show | 95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.100-17712A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934426 | ||||||
| chr14:69934442
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-17696A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934442 | ||||||
| chr14:69934597
|
C | G | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100-17541C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934597 | ||||||
| chr14:69934713
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0118others(7): Show | 11 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-17425A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934713 | ||||||
| chr14:69934732
|
C | T | 2 | a0001c0001t0007g0097a0001c0001t0007g0100 | 2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-17406C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934732 | ||||||
| chr14:69934810
|
A | G | 1 | a0001c0001t0007g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.100-17328A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934810 | ||||||
| chr14:69934920
|
C | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-17218C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69934920 | ||||||
| chr14:69935038
|
T | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(166): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.100-17100T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935038 | ||||||
| chr14:69935097
|
G | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0059others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.100-17041G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935097 | ||||||
| chr14:69935106
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0007g0095others(1): Show | 4 | HG02486.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17032A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935106 | ||||||
| chr14:69935168
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100-16970T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935168 | ||||||
| chr14:69935203
|
T | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-16935T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935203 | ||||||
| chr14:69935224
|
G | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01106.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-16914G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935224 | ||||||
| chr14:69935374
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-16764T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935374 | ||||||
| chr14:69935393
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.100-16745C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935393 | ||||||
| chr14:69935444
|
C | T | 1 | a0001c0001t0010g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100-16694C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935444 | ||||||
| chr14:69935578
|
G | A | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-16560G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69935578 | ||||||
| chr14:69935680
|
C | CG | 7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0128others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-16453dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69935680 | |||||
| chr14:69936005
|
G | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0059others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.100-16133G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936005 | ||||||
| chr14:69936015
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-16123G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936015 | ||||||
| chr14:69936045
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-16093A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936045 | ||||||
| chr14:69936098
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-16040G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936098 | ||||||
| chr14:69936102
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(115): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.100-16036T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936102 | ||||||
| chr14:69936137
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100-16001C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936137 | ||||||
| chr14:69936206
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.100-15932G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936206 | ||||||
| chr14:69936587
|
T | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(124): Show | 130 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.100-15551T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936587 | ||||||
| chr14:69936789
|
AAACCCAT others(4): Show |
A | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-15339_100-1532 others(15): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69936789 | |||||
| chr14:69936812
|
G | A | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(123): Show | 129 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.100-15326G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936812 | ||||||
| chr14:69936830
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0087others(17): Show | 22 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-15308C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69936830 | ||||||
| chr14:69936870
|
CTT | C | 24 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0058others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-15266_100-1526 others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69936870 | |||||
| chr14:69937145
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-14993T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937145 | ||||||
| chr14:69937243
|
G | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0027g0036others(1): Show | 4 | HG01106.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-14895G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937243 | ||||||
| chr14:69937287
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-14851A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937287 | ||||||
| chr14:69937603
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-14535C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937603 | ||||||
| chr14:69937619
|
T | C | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(114): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-14519T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937619 | ||||||
| chr14:69937625
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0214others(5): Show | 8 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-14513C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937625 | ||||||
| chr14:69937690
|
G | A | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-14448G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937690 | ||||||
| chr14:69937696
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(11): Show | 15 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-14442A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937696 | ||||||
| chr14:69937728
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(24): Show | 28 | HG01069.hp2 HG01106.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-14410C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937728 | ||||||
| chr14:69937834
|
A | G | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(4): Show | 7 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-14304A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937834 | ||||||
| chr14:69937957
|
C | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(171): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.100-14181C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69937957 | ||||||
| chr14:69938197
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0015g0054others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-13941T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938197 | ||||||
| chr14:69938334
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.100-13804G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938334 | ||||||
| chr14:69938363
|
G | A | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100-13775G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938363 | ||||||
| chr14:69938500
|
G | GA | 143 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0020others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.100-13638_100-1363 others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938500 | ||||||
| chr14:69938524
|
G | A | 2 | a0001c0004t0001g0265a0001c0004t0004g0105 | 2 | HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.100-13614G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938524 | ||||||
| chr14:69938669
|
A | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0065others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-13469A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938669 | ||||||
| chr14:69938997
|
A | G | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100-13141A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69938997 | ||||||
| chr14:69939150
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.100-12988C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939150 | ||||||
| chr14:69939231
|
G | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-12907G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939231 | ||||||
| chr14:69939274
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(1): Show | 4 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-12864A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939274 | ||||||
| chr14:69939303
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-12835G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939303 | ||||||
| chr14:69939342
|
G | T | 2 | a0001c0001t0006g0080a0001c0001t0030g0093 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.100-12796G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939342 | ||||||
| chr14:69939831
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100-12307C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939831 | ||||||
| chr14:69939833
|
T | C | 142 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0020others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.100-12305T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939833 | ||||||
| chr14:69939838
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-12300G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939838 | ||||||
| chr14:69939854
|
G | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(156): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.100-12284G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939854 | ||||||
| chr14:69939961
|
G | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0110others(13): Show | 18 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-12177G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69939961 | ||||||
| chr14:69940187
|
G | A | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-11951G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69940187 | ||||||
| chr14:69940306
|
T | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0110others(13): Show | 18 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-11832T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69940306 | ||||||
| chr14:69940615
|
TTC | T | 24 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0058others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-11521_100-1152 others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69940615 | |||||
| chr14:69940743
|
A | AT | 16 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0110others(13): Show | 18 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-11387dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69940743 | |||||
| chr14:69940793
|
TC | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(36): Show | 42 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.100-11342delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69940793 | |||||
| chr14:69940871
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0005g0239 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.100-11267A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69940871 | ||||||
| chr14:69941001
|
A | T | 38 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0140others(35): Show | 38 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-11137A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941001 | ||||||
| chr14:69941052
|
T | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0020others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.100-11086T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941052 | ||||||
| chr14:69941066
|
T | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0264a0001c0001t0002g0003others(3): Show | 7 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-11072T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941066 | ||||||
| chr14:69941093
|
GTCC | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0108others(10): Show | 14 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-11040_100-1103 others(7): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69941093 | |||||
| chr14:69941143
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100-10995C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941143 | ||||||
| chr14:69941161
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0143others(4): Show | 7 | NA18940.hp2 NA18984.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-10977C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941161 | ||||||
| chr14:69941234
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0264a0001c0001t0002g0003others(3): Show | 7 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-10904G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941234 | ||||||
| chr14:69941312
|
G | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(24): Show | 27 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10826G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941312 | ||||||
| chr14:69941341
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100-10797G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941341 | ||||||
| chr14:69941406
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.100-10732G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941406 | ||||||
| chr14:69941493
|
G | A | 1 | a0001c0002t0002g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-10645G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941493 | ||||||
| chr14:69941595
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-10543C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941595 | ||||||
| chr14:69941681
|
G | A | 3 | a0001c0001t0001g0254a0001c0002t0002g0245a0001c0002t0002g0248 | 3 | NA18981.hp2 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.100-10457G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941681 | ||||||
| chr14:69941776
|
G | C | 181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(178): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.100-10362G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941776 | ||||||
| chr14:69941949
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG01074.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-10189C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941949 | ||||||
| chr14:69941954
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-10184C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69941954 | ||||||
| chr14:69942010
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0215a0001c0001t0001g0228others(2): Show | 5 | HG00642.hp2 HG01099.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-10128G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69942010 | ||||||
| chr14:69942440
|
G | A | 118 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0028others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.100-9698G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69942440 | ||||||
| chr14:69942561
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0007g0095others(1): Show | 4 | HG02622.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-9577C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69942561 | ||||||
| chr14:69942786
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.100-9352A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69942786 | ||||||
| chr14:69942858
|
G | C | 1 | a0001c0003t0002g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.100-9280G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69942858 | ||||||
| chr14:69943015
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-9123G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943015 | ||||||
| chr14:69943058
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100-9080C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943058 | ||||||
| chr14:69943059
|
T | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.100-9079T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943059 | ||||||
| chr14:69943205
|
G | A | 1 | a0001c0001t0006g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-8933G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943205 | ||||||
| chr14:69943224
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 19 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-8914T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943224 | ||||||
| chr14:69943308
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0006g0230others(2): Show | 6 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-8830T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943308 | ||||||
| chr14:69943349
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100-8789G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943349 | ||||||
| chr14:69943509
|
G | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0001g0108others(18): Show | 23 | HG00741.hp1 HG01069.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.100-8629G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943509 | ||||||
| chr14:69943510
|
G | A | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-8628G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943510 | ||||||
| chr14:69943676
|
TC | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 129 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.100-8454delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69943676 | |||||
| chr14:69943682
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.100-8456C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943682 | ||||||
| chr14:69943684
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100-8454C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943684 | ||||||
| chr14:69943766
|
A | T | 49 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095others(46): Show | 49 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.100-8372A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943766 | ||||||
| chr14:69943781
|
C | G | 2 | a0001c0002t0001g0137a0001c0002t0002g0180 | 2 | NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.100-8357C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943781 | ||||||
| chr14:69943843
|
G | A | 3 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0017g0176 | 3 | HG01109.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100-8295G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69943843 | ||||||
| chr14:69944050
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-8088T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944050 | ||||||
| chr14:69944157
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(2): Show | 5 | NA18940.hp2 NA18956.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-7981G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944157 | ||||||
| chr14:69944373
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.100-7765T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944373 | ||||||
| chr14:69944380
|
G | T | 49 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095others(46): Show | 49 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.100-7758G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944380 | ||||||
| chr14:69944381
|
A | T | 49 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095others(46): Show | 49 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.100-7757A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944381 | ||||||
| chr14:69944620
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0264 | 2 | HG00733.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.100-7518A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944620 | ||||||
| chr14:69944629
|
G | T | 43 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(40): Show | 43 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.100-7509G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944629 | ||||||
| chr14:69944638
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0012g0001others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-7500C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944638 | ||||||
| chr14:69944742
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0005g0189a0001c0001t0007g0032others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7396C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944742 | ||||||
| chr14:69944742
|
C | T | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100-7396C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944742 | ||||||
| chr14:69944774
|
G | T | 3 | a0001c0001t0001g0048a0001c0001t0020g0096a0006c0010t0001g0035 | 3 | HG02895.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-7364G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944774 | ||||||
| chr14:69944782
|
G | C | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100-7356G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944782 | ||||||
| chr14:69944882
|
AT | A | 4 | a0001c0005t0001g0033a0001c0005t0001g0040a0001c0005t0001g0069others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7249delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69944882 | |||||
| chr14:69944979
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0032g0170 | 4 | HG01433.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7159A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69944979 | ||||||
| chr14:69945247
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0118others(4): Show | 8 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-6891A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945247 | ||||||
| chr14:69945252
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0031g0053 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-6886G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945252 | ||||||
| chr14:69945401
|
C | G | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-6737C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945401 | ||||||
| chr14:69945529
|
A | G | 1 | a0001c0001t0011g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-6609A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945529 | ||||||
| chr14:69945577
|
T | A | 9 | a0001c0002t0002g0138a0001c0002t0002g0169a0001c0002t0002g0185others(6): Show | 9 | HG00639.hp2 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-6561T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945577 | ||||||
| chr14:69945595
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.100-6543A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69945595 | ||||||
| chr14:69946161
|
C | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 132 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.100-5977C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946161 | ||||||
| chr14:69946282
|
C | G | 1 | a0001c0001t0007g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-5856C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946282 | ||||||
| chr14:69946329
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0041others(81): Show | 85 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.100-5809A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946329 | ||||||
| chr14:69946343
|
C | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-5795C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946343 | ||||||
| chr14:69946644
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0235 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.100-5494C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946644 | ||||||
| chr14:69946665
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.100-5473G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69946665 | ||||||
| chr14:69947085
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.100-5053C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947085 | ||||||
| chr14:69947087
|
G | GCCGGCCT others(5): Show |
1 | a0001c0001t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-5049_100-5048i others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTT | 63 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0025others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.100-5012_100-5009d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTTCCC others(9): Show |
1 | a0001c0001t0003g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-5045_100-5044i others(18): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTTCCT others(1): Show |
44 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0041others(41): Show | 46 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-5016_100-5009d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTTCCT others(5): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(19): Show | 24 | HG00642.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-5020_100-5009d others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTTCCT others(9): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02074.hp1 HG02615.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-5024_100-5009d others(18): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
G | GCCTTCCT others(13): Show |
2 | a0001c0001t0001g0020a0001c0001t0005g0221 | 2 | HG02451.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.100-5028_100-5009d others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
GCCTT | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 23 | HG00280.hp2 HG00597.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-5012_100-5009d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
GCCTTCCT others(1): Show |
G | 6 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0126others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-5016_100-5009d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947087
|
GCCTTCCT others(5): Show |
G | 2 | a0001c0002t0002g0244a0006c0010t0001g0035 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-5020_100-5009d others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 69947087 | |||||
| chr14:69947190
|
C | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.100-4948C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947190 | ||||||
| chr14:69947224
|
A | G | 3 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0017g0176 | 3 | HG01109.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100-4914A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947224 | ||||||
| chr14:69947301
|
C | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0050others(27): Show | 30 | HG01074.hp2 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.100-4837C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947301 | ||||||
| chr14:69947331
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-4807G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947331 | ||||||
| chr14:69947409
|
A | T | 2 | a0001c0002t0001g0257a0001c0002t0002g0129 | 2 | NA18953.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.100-4729A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947409 | ||||||
| chr14:69947545
|
G | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0152a0001c0001t0001g0154 | 3 | HG01433.hp2 HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.100-4593G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947545 | ||||||
| chr14:69947725
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-4413G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947725 | ||||||
| chr14:69947729
|
A | T | 1 | a0001c0002t0002g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.100-4409A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947729 | ||||||
| chr14:69947902
|
G | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 115 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.100-4236G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947902 | ||||||
| chr14:69947979
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0033g0043others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-4159C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69947979 | ||||||
| chr14:69948056
|
G | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.100-4082G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948056 | ||||||
| chr14:69948117
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0050others(26): Show | 29 | HG01074.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-4021A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948117 | ||||||
| chr14:69948207
|
C | T | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3931C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948207 | ||||||
| chr14:69948528
|
T | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 130 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.100-3610T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948528 | ||||||
| chr14:69948562
|
C | T | 1 | a0001c0004t0006g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-3576C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948562 | ||||||
| chr14:69948572
|
A | G | 9 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(6): Show | 11 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-3566A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948572 | ||||||
| chr14:69948642
|
G | A | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 115 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.100-3496G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948642 | ||||||
| chr14:69948822
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100-3316T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69948822 | ||||||
| chr14:69949012
|
A | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.100-3126A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949012 | ||||||
| chr14:69949080
|
C | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 18 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-3058C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949080 | ||||||
| chr14:69949185
|
C | T | 9 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(6): Show | 11 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-2953C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949185 | ||||||
| chr14:69949313
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100-2825C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949313 | ||||||
| chr14:69949524
|
G | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2614G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949524 | ||||||
| chr14:69949557
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0033g0043a0002c0013t0023g0027 | 3 | HG02258.hp2 HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.100-2581A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949557 | ||||||
| chr14:69949618
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0128a0001c0001t0007g0032others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-2520G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949618 | ||||||
| chr14:69949634
|
G | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0063others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-2504G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949634 | ||||||
| chr14:69949642
|
G | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2496G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949642 | ||||||
| chr14:69949673
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-2465T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949673 | ||||||
| chr14:69949725
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0041others(77): Show | 81 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.100-2413G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949725 | ||||||
| chr14:69949725
|
G | C | 1 | a0001c0002t0002g0138 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100-2413G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949725 | ||||||
| chr14:69949803
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-2335G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69949803 | ||||||
| chr14:69950001
|
G | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 115 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.100-2137G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69950001 | ||||||
| chr14:69950160
|
A | G | 1 | a0001c0001t0003g0016 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.100-1978A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69950160 | ||||||
| chr14:69950570
|
C | G | 9 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(6): Show | 11 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-1568C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69950570 | ||||||
| chr14:69950762
|
C | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(12): Show | 15 | HG00280.hp1 HG00639.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-1376C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69950762 | ||||||
| chr14:69951071
|
G | T | 1 | a0001c0001t0005g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-1067G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951071 | ||||||
| chr14:69951075
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0050others(27): Show | 30 | HG01074.hp2 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.100-1063G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951075 | ||||||
| chr14:69951129
|
A | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 115 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.100-1009A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951129 | ||||||
| chr14:69951227
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 18 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-911C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951227 | ||||||
| chr14:69951448
|
G | T | 26 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0063others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-690G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951448 | ||||||
| chr14:69951478
|
C | A | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-660C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951478 | ||||||
| chr14:69951876
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-262G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69951876 | ||||||
| chr14:69952081
|
G | A | 13 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0065others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-57G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 1/11 | chr14 | 69952081 | ||||||
| chr14:69952373
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.265+70G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69952373 | ||||||
| chr14:69952392
|
T | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+89T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69952392 | ||||||
| chr14:69952549
|
G | A | 46 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0017g0176others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.265+246G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69952549 | ||||||
| chr14:69952637
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.265+334G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69952637 | ||||||
| chr14:69952959
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0005g0219others(1): Show | 4 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-461C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69952959 | ||||||
| chr14:69953149
|
A | AT | 67 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(64): Show | 69 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.266-262dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 69953149 | |||||
| chr14:69953151
|
T | TG | 27 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(24): Show | 27 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.266-269_266-268ins others(1): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69953151 | ||||||
| chr14:69953247
|
C | T | 1 | a0001c0003t0002g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.266-173C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 2/11 | chr14 | 69953247 | ||||||
| chr14:69953572
|
C | T | 1 | a0001c0004t0001g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.378+40C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69953572 | ||||||
| chr14:69953884
|
T | C | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+352T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69953884 | ||||||
| chr14:69953907
|
C | T | 1 | a0001c0003t0004g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.378+375C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69953907 | ||||||
| chr14:69954002
|
G | GGAGTGTG others(1): Show |
128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.378+480_378+487dup others(8): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69954002 | |||||
| chr14:69954012
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.378+487_378+488ins others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69954012 | |||||
| chr14:69954141
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.378+609G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954141 | ||||||
| chr14:69954221
|
C | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0118others(2): Show | 6 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+689C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954221 | ||||||
| chr14:69954660
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.378+1128A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954660 | ||||||
| chr14:69954718
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0231 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.378+1186A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954718 | ||||||
| chr14:69954772
|
G | C | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.378+1240G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954772 | ||||||
| chr14:69954894
|
T | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0206others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+1362T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69954894 | ||||||
| chr14:69955009
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.378+1477T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955009 | ||||||
| chr14:69955105
|
T | A | 1 | a0001c0004t0004g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.378+1573T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955105 | ||||||
| chr14:69955114
|
T | C | 59 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0125others(56): Show | 59 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.378+1582T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955114 | ||||||
| chr14:69955144
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.378+1612G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955144 | ||||||
| chr14:69955509
|
A | G | 1 | a0001c0001t0006g0230 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.378+1977A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955509 | ||||||
| chr14:69955648
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+2116T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955648 | ||||||
| chr14:69955688
|
GA | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 134 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+2165delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69955688 | |||||
| chr14:69955697
|
A | C | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.378+2165A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955697 | ||||||
| chr14:69955762
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.378+2230T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955762 | ||||||
| chr14:69955799
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+2267T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955799 | ||||||
| chr14:69955863
|
C | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2331C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955863 | ||||||
| chr14:69955965
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+2433G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69955965 | ||||||
| chr14:69956161
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(92): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.378+2629A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956161 | ||||||
| chr14:69956253
|
C | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+2721C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956253 | ||||||
| chr14:69956447
|
G | C | 1 | a0001c0001t0004g0013 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.378+2915G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956447 | ||||||
| chr14:69956448
|
C | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+2916C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956448 | ||||||
| chr14:69956448
|
C | CT | 7 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0134others(4): Show | 7 | HG01081.hp1 HG03098.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2934dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69956448 | |||||
| chr14:69956448
|
C | CTT | 79 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(76): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.378+2933_378+2934d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69956448 | |||||
| chr14:69956448
|
C | CTTT | 7 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095others(4): Show | 7 | HG01106.hp2 HG01255.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+2932_378+2934d others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69956448 | |||||
| chr14:69956448
|
C | T | 1 | a0001c0001t0004g0013 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.378+2916C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956448 | ||||||
| chr14:69956448
|
CT | C | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(12): Show | 16 | HG00741.hp1 HG01069.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.378+2934delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69956448 | |||||
| chr14:69956504
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.378+2972T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956504 | ||||||
| chr14:69956540
|
G | A | 48 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(45): Show | 48 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.378+3008G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956540 | ||||||
| chr14:69956604
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.378+3072G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956604 | ||||||
| chr14:69956610
|
T | C | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.378+3078T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956610 | ||||||
| chr14:69956620
|
A | G | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378+3088A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956620 | ||||||
| chr14:69956781
|
T | C | 1 | a0001c0003t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.378+3249T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956781 | ||||||
| chr14:69956970
|
T | A | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 134 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+3438T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69956970 | ||||||
| chr14:69956984
|
C | CT | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+3453dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69956984 | |||||
| chr14:69957034
|
A | C | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+3502A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957034 | ||||||
| chr14:69957046
|
C | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+3514C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957046 | ||||||
| chr14:69957501
|
C | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 134 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+3969C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957501 | ||||||
| chr14:69957581
|
G | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+4049G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957581 | ||||||
| chr14:69957685
|
C | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(92): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.378+4153C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957685 | ||||||
| chr14:69957686
|
A | C | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.378+4154A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957686 | ||||||
| chr14:69957736
|
G | C | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 134 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+4204G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957736 | ||||||
| chr14:69957762
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.378+4230A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957762 | ||||||
| chr14:69957819
|
C | G | 1 | a0001c0001t0003g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.378+4287C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957819 | ||||||
| chr14:69957839
|
T | C | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+4307T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957839 | ||||||
| chr14:69957920
|
A | T | 1 | a0001c0001t0004g0013 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.378+4388A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957920 | ||||||
| chr14:69957931
|
C | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.378+4399C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69957931 | ||||||
| chr14:69958000
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+4468G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958000 | ||||||
| chr14:69958233
|
C | G | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.378+4701C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958233 | ||||||
| chr14:69958288
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+4756A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958288 | ||||||
| chr14:69958789
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.378+5257A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958789 | ||||||
| chr14:69958791
|
C | T | 1 | a0001c0001t0014g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.378+5259C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958791 | ||||||
| chr14:69958813
|
T | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+5281T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958813 | ||||||
| chr14:69958855
|
C | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+5323C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958855 | ||||||
| chr14:69958892
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.378+5360A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69958892 | ||||||
| chr14:69959002
|
T | C | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 134 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+5470T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959002 | ||||||
| chr14:69959010
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+5478T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959010 | ||||||
| chr14:69959081
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0005g0219others(1): Show | 4 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+5549T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959081 | ||||||
| chr14:69959096
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+5564G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959096 | ||||||
| chr14:69959415
|
C | T | 8 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+5883C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959415 | ||||||
| chr14:69959664
|
A | ATTGCATA others(24): Show |
6 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(3): Show | 6 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+6162_378+6192d others(33): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69959664 | |||||
| chr14:69959664
|
ATTGCATA others(24): Show |
A | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.378+6162_378+6192d others(33): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69959664 | |||||
| chr14:69959836
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0152others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+6304T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959836 | ||||||
| chr14:69959884
|
A | G | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+6352A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959884 | ||||||
| chr14:69959951
|
C | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+6419C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69959951 | ||||||
| chr14:69960102
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.378+6570A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960102 | ||||||
| chr14:69960258
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.378+6726G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960258 | ||||||
| chr14:69960551
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.378+7019G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960551 | ||||||
| chr14:69960817
|
G | GTAAACT | 90 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.378+7285_378+7286i others(8): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960817 | ||||||
| chr14:69960911
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7379A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960911 | ||||||
| chr14:69960929
|
A | G | 1 | a0001c0001t0006g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.378+7397A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960929 | ||||||
| chr14:69960955
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.378+7423T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69960955 | ||||||
| chr14:69961140
|
T | C | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7608T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961140 | ||||||
| chr14:69961190
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.378+7658G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961190 | ||||||
| chr14:69961268
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0005g0219others(1): Show | 4 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+7736T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961268 | ||||||
| chr14:69961270
|
G | GTA | 5 | a0001c0001t0001g0065a0001c0001t0001g0206a0001c0001t0001g0217others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+7739_378+7740i others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961270 | |||||
| chr14:69961270
|
GTGTATAT others(1): Show |
G | 5 | a0001c0001t0001g0071a0001c0001t0001g0215a0001c0001t0001g0228others(2): Show | 5 | HG02486.hp2 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+7740_378+7747d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961270 | |||||
| chr14:69961270
|
GTGTATAT others(5): Show |
G | 2 | a0001c0001t0015g0054a0001c0001t0016g0078 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.378+7740_378+7751d others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961270 | |||||
| chr14:69961270
|
GTGTATAT others(15): Show |
G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+7740_378+7761d others(24): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961270 | |||||
| chr14:69961270
|
GTGTATAT others(27): Show |
G | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.378+7740_378+7773d others(36): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961270 | |||||
| chr14:69961272
|
G | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0206a0001c0001t0001g0217others(3): Show | 6 | HG01175.hp2 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+7740G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961272 | ||||||
| chr14:69961272
|
G | GTA | 33 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0070others(30): Show | 33 | HG00280.hp1 HG00438.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.378+7786_378+7787d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
G | GTATA | 18 | a0001c0001t0001g0049a0001c0001t0001g0076a0001c0001t0001g0121others(15): Show | 18 | HG01934.hp2 HG02145.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+7784_378+7787d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
G | GTATATA | 13 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0048others(10): Show | 13 | HG00323.hp1 HG00639.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.378+7782_378+7787d others(8): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0044others(4): Show | 7 | HG02698.hp1 HG02698.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+7780_378+7787d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0162a0001c0006t0001g0220a0001c0006t0001g0233 | 3 | HG00642.hp2 HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.378+7778_378+7787d others(12): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
G | GTGTGTAT others(3): Show |
1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.378+7741_378+7742i others(12): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTA | G | 26 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0058others(23): Show | 26 | HG00597.hp1 HG00733.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+7786_378+7787d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATA | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(13): Show | 16 | HG00140.hp1 HG01074.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.378+7784_378+7787d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATA | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0091a0001c0001t0001g0128others(5): Show | 8 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+7782_378+7787d others(8): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0126others(4): Show | 7 | HG00280.hp2 HG01167.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+7780_378+7787d others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0179a0001c0002t0002g0234a0001c0002t0002g0236 | 3 | HG00639.hp2 HG00642.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.378+7778_378+7787d others(12): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0001g0098a0001c0001t0003g0089 | 2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.378+7776_378+7787d others(14): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0213a0001c0002t0002g0209 | 2 | HG00423.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.378+7774_378+7787d others(16): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(9): Show |
G | 8 | a0001c0001t0001g0264a0001c0002t0002g0151a0001c0002t0002g0194others(5): Show | 8 | HG00597.hp2 HG01255.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+7772_378+7787d others(18): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(11): Show |
G | 34 | a0001c0001t0001g0188a0001c0001t0001g0192a0001c0002t0001g0117others(31): Show | 34 | HG00140.hp2 HG00438.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.378+7770_378+7787d others(20): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(13): Show |
G | 4 | a0001c0001t0001g0187a0001c0001t0008g0002a0001c0002t0002g0156others(1): Show | 5 | HG00741.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+7768_378+7787d others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(15): Show |
G | 4 | a0001c0001t0001g0028a0001c0001t0008g0057a0001c0001t0008g0062others(1): Show | 4 | HG02647.hp1 HG03486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7766_378+7787d others(24): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961272
|
GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0029a0001c0003t0002g0246 | 2 | HG02074.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.378+7764_378+7787d others(26): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69961272 | |||||
| chr14:69961274
|
A | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(10): Show | 13 | HG01433.hp2 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.378+7742A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961274 | ||||||
| chr14:69961276
|
A | G | 2 | a0001c0005t0001g0040a0002c0013t0023g0027 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.378+7744A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961276 | ||||||
| chr14:69961278
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0009g0037a0001c0001t0009g0038others(1): Show | 4 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7746A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961278 | ||||||
| chr14:69961280
|
A | G | 1 | a0001c0007t0003g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378+7748A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961280 | ||||||
| chr14:69961282
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0031g0053a0001c0007t0003g0008 | 3 | HG01884.hp2 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.378+7750A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961282 | ||||||
| chr14:69961286
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0231 | 2 | HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.378+7754A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961286 | ||||||
| chr14:69961288
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0213 | 2 | HG00642.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.378+7756A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961288 | ||||||
| chr14:69961290
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.378+7758A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961290 | ||||||
| chr14:69961296
|
A | G | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+7764A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961296 | ||||||
| chr14:69961383
|
G | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.378+7851G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961383 | ||||||
| chr14:69961432
|
G | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0206a0001c0001t0001g0215others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+7900G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961432 | ||||||
| chr14:69961490
|
C | T | 44 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(41): Show | 44 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.378+7958C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961490 | ||||||
| chr14:69961610
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.378+8078G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961610 | ||||||
| chr14:69961805
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0003g0088a0001c0001t0007g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.378+8273T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961805 | ||||||
| chr14:69961870
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.378+8338C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961870 | ||||||
| chr14:69961872
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0206others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+8340G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961872 | ||||||
| chr14:69961927
|
A | G | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.378+8395A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69961927 | ||||||
| chr14:69962113
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.378+8581T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962113 | ||||||
| chr14:69962174
|
A | G | 1 | a0001c0001t0014g0106 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.378+8642A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962174 | ||||||
| chr14:69962353
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.378+8821T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962353 | ||||||
| chr14:69962369
|
C | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(87): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.378+8837C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962369 | ||||||
| chr14:69962393
|
G | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0118others(5): Show | 9 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+8861G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962393 | ||||||
| chr14:69962408
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(29): Show | 33 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.378+8876C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962408 | ||||||
| chr14:69962444
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+8912G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962444 | ||||||
| chr14:69962560
|
C | T | 5 | a0001c0001t0002g0181a0001c0001t0003g0238a0001c0001t0003g0241others(2): Show | 5 | NA18969.hp2 NA18988.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+9028C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962560 | ||||||
| chr14:69962673
|
C | A | 87 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+9141C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962673 | ||||||
| chr14:69962797
|
G | A | 2 | a0001c0001t0003g0260a0001c0003t0002g0145 | 2 | HG00323.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.378+9265G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962797 | ||||||
| chr14:69962799
|
A | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+9267A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962799 | ||||||
| chr14:69962834
|
C | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+9302C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962834 | ||||||
| chr14:69962931
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0005g0189 | 2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.378+9399T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962931 | ||||||
| chr14:69962959
|
C | T | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.378+9427C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962959 | ||||||
| chr14:69962975
|
A | G | 1 | a0001c0003t0002g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.378+9443A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69962975 | ||||||
| chr14:69963097
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+9565A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963097 | ||||||
| chr14:69963102
|
A | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+9570A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963102 | ||||||
| chr14:69963118
|
T | C | 2 | a0001c0002t0002g0245a0001c0002t0002g0248 | 2 | NA18981.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.378+9586T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963118 | ||||||
| chr14:69963148
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+9616T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963148 | ||||||
| chr14:69963164
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0033g0043others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+9632G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963164 | ||||||
| chr14:69963263
|
G | A | 1 | a0001c0001t0007g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378+9731G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963263 | ||||||
| chr14:69963282
|
G | A | 87 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+9750G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963282 | ||||||
| chr14:69963315
|
G | T | 28 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 28 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.378+9783G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963315 | ||||||
| chr14:69963394
|
G | T | 1 | a0004c0012t0001g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.378+9862G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963394 | ||||||
| chr14:69963739
|
A | G | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378+10207A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963739 | ||||||
| chr14:69963851
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.378+10319C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963851 | ||||||
| chr14:69963913
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0152others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+10381C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69963913 | ||||||
| chr14:69964021
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0012g0001others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+10489G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964021 | ||||||
| chr14:69964043
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+10511T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964043 | ||||||
| chr14:69964074
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0004g0047 | 2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.378+10542A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964074 | ||||||
| chr14:69964203
|
T | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0067others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.378+10671T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964203 | ||||||
| chr14:69964236
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0228 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.378+10704C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964236 | ||||||
| chr14:69964380
|
C | CT | 97 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(94): Show | 99 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.378+10863dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69964380 | |||||
| chr14:69964380
|
CT | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG01167.hp1 HG01257.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+10863delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69964380 | |||||
| chr14:69964478
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.378+10946C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964478 | ||||||
| chr14:69964538
|
C | T | 1 | a0001c0002t0002g0180 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.378+11006C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964538 | ||||||
| chr14:69964559
|
A | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0001g0213others(3): Show | 6 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+11027A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964559 | ||||||
| chr14:69964567
|
C | T | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.378+11035C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964567 | ||||||
| chr14:69964647
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.379-11068A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964647 | ||||||
| chr14:69964697
|
C | A | 1 | a0001c0001t0007g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379-11018C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964697 | ||||||
| chr14:69964738
|
T | C | 62 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0125others(59): Show | 63 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.379-10977T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964738 | ||||||
| chr14:69964754
|
A | G | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.379-10961A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964754 | ||||||
| chr14:69964916
|
T | G | 1 | a0001c0002t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.379-10799T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69964916 | ||||||
| chr14:69965006
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.379-10709T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965006 | ||||||
| chr14:69965144
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379-10571G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965144 | ||||||
| chr14:69965158
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.379-10557A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965158 | ||||||
| chr14:69965207
|
A | G | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-10508A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965207 | ||||||
| chr14:69965286
|
CA | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-10428delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965286 | ||||||
| chr14:69965377
|
A | AAAT | 3 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0026g0072 | 3 | HG02486.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.379-10311_379-1030 others(7): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965377
|
A | AAATAAT | 4 | a0001c0001t0001g0065a0001c0001t0003g0088a0001c0001t0005g0219others(1): Show | 4 | HG01175.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-10314_379-1030 others(10): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965377
|
A | AAATAATA others(5): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0215 | 2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.379-10320_379-1030 others(16): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965377
|
A | AAATAATA others(8): Show |
4 | a0001c0001t0001g0108a0001c0001t0001g0206a0001c0001t0001g0217others(1): Show | 4 | HG01069.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-10323_379-1030 others(19): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965377
|
A | AAATAATA others(11): Show |
13 | a0001c0001t0001g0125a0001c0001t0001g0155a0001c0001t0001g0228others(10): Show | 14 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-10326_379-1030 others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965377
|
A | AAATAATA others(14): Show |
6 | a0001c0001t0001g0041a0001c0001t0005g0189a0001c0001t0008g0002others(3): Show | 7 | HG00438.hp1 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-10329_379-1030 others(25): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965377 | |||||
| chr14:69965404
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.379-10311T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965404 | ||||||
| chr14:69965404
|
T | TAATAATA others(8): Show |
3 | a0001c0002t0002g0151a0001c0002t0002g0244a0005c0008t0002g0251 | 3 | HG01255.hp1 HG02015.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.379-10309_379-1030 others(19): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965404 | |||||
| chr14:69965404
|
T | TAATAATA others(11): Show |
1 | a0001c0004t0005g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.379-10309_379-1030 others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965404 | |||||
| chr14:69965404
|
T | TAATAATA others(11): Show |
11 | a0001c0002t0001g0137a0001c0002t0002g0138a0001c0002t0002g0169others(8): Show | 11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-10309_379-1030 others(22): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965404 | |||||
| chr14:69965404
|
T | TAATAATA others(14): Show |
23 | a0001c0002t0001g0117a0001c0002t0001g0257a0001c0002t0002g0012others(20): Show | 23 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.379-10309_379-1030 others(25): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965404 | |||||
| chr14:69965404
|
T | TAATAATA others(17): Show |
3 | a0001c0002t0002g0139a0001c0002t0002g0195a0001c0004t0006g0202 | 3 | NA18944.hp1 NA19066.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.379-10309_379-1030 others(28): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69965404 | |||||
| chr14:69965503
|
A | G | 27 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0063others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.379-10212A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965503 | ||||||
| chr14:69965621
|
T | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0108a0001c0001t0001g0125others(15): Show | 19 | HG00741.hp1 HG01069.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-10094T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965621 | ||||||
| chr14:69965635
|
T | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0108a0001c0001t0001g0125others(15): Show | 19 | HG00741.hp1 HG01069.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-10080T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965635 | ||||||
| chr14:69965773
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.379-9942A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69965773 | ||||||
| chr14:69966102
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-9613G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966102 | ||||||
| chr14:69966430
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01074.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-9285T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966430 | ||||||
| chr14:69966605
|
C | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(4): Show | 8 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-9110C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966605 | ||||||
| chr14:69966680
|
T | C | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-9035T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966680 | ||||||
| chr14:69966712
|
A | G | 1 | a0001c0001t0003g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.379-9003A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966712 | ||||||
| chr14:69966810
|
C | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 28 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.379-8905C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966810 | ||||||
| chr14:69966935
|
A | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-8780A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69966935 | ||||||
| chr14:69967041
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-8674G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967041 | ||||||
| chr14:69967243
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0033g0043 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.379-8472A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967243 | ||||||
| chr14:69967465
|
A | AT | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-8242dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69967465 | |||||
| chr14:69967554
|
CCAAAAGA | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(1): Show | 4 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-8160_379-8154d others(9): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967554 | ||||||
| chr14:69967562
|
T | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(1): Show | 4 | HG01081.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-8153T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967562 | ||||||
| chr14:69967575
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.379-8140G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967575 | ||||||
| chr14:69967882
|
G | T | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-7833G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967882 | ||||||
| chr14:69967942
|
A | G | 76 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(73): Show | 76 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.379-7773A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69967942 | ||||||
| chr14:69968038
|
G | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(94): Show | 98 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.379-7677G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968038 | ||||||
| chr14:69968151
|
T | C | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.379-7564T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968151 | ||||||
| chr14:69968246
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.379-7469G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968246 | ||||||
| chr14:69968270
|
G | C | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-7445G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968270 | ||||||
| chr14:69968280
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.379-7435C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968280 | ||||||
| chr14:69968421
|
G | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0206others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-7294G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968421 | ||||||
| chr14:69968431
|
G | T | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-7284G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968431 | ||||||
| chr14:69968703
|
C | CAA | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-7009_379-7008d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69968703 | |||||
| chr14:69968733
|
T | C | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-6982T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968733 | ||||||
| chr14:69968791
|
C | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(29): Show | 33 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-6924C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968791 | ||||||
| chr14:69968813
|
C | T | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 135 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.379-6902C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968813 | ||||||
| chr14:69968988
|
T | A | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-6727T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69968988 | ||||||
| chr14:69969027
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379-6688A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969027 | ||||||
| chr14:69969047
|
G | A | 1 | a0001c0001t0005g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.379-6668G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969047 | ||||||
| chr14:69969225
|
G | A | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.379-6490G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969225 | ||||||
| chr14:69969260
|
G | A | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-6455G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969260 | ||||||
| chr14:69969358
|
A | T | 1 | a0001c0002t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.379-6357A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969358 | ||||||
| chr14:69969454
|
GCAGGAA | G | 21 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(18): Show | 22 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.379-6255_379-6250d others(8): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69969454 | |||||
| chr14:69969527
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-6188G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969527 | ||||||
| chr14:69969529
|
C | T | 46 | a0001c0001t0001g0079a0001c0001t0014g0173a0001c0002t0001g0117others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.379-6186C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969529 | ||||||
| chr14:69969629
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-6086T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969629 | ||||||
| chr14:69969994
|
A | G | 15 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0125others(12): Show | 15 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-5721A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69969994 | ||||||
| chr14:69970086
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.379-5629A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970086 | ||||||
| chr14:69970161
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0206others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.379-5554G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970161 | ||||||
| chr14:69970360
|
A | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(32): Show | 35 | HG01074.hp2 HG01106.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.379-5355A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970360 | ||||||
| chr14:69970454
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0004g0047 | 2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.379-5261T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970454 | ||||||
| chr14:69970521
|
T | C | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-5194T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970521 | ||||||
| chr14:69970577
|
G | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0087others(4): Show | 7 | HG01106.hp2 HG01175.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-5138G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970577 | ||||||
| chr14:69970586
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-5129T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970586 | ||||||
| chr14:69970735
|
AC | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-4975delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69970735 | |||||
| chr14:69970790
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0005g0103a0001c0001t0005g0104others(1): Show | 4 | HG01192.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-4925G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970790 | ||||||
| chr14:69970883
|
A | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-4832A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69970883 | ||||||
| chr14:69971014
|
C | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-4701C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971014 | ||||||
| chr14:69971041
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379-4674C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971041 | ||||||
| chr14:69971109
|
C | T | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.379-4606C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971109 | ||||||
| chr14:69971432
|
T | C | 44 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(41): Show | 44 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.379-4283T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971432 | ||||||
| chr14:69971570
|
C | T | 1 | a0001c0001t0014g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.379-4145C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971570 | ||||||
| chr14:69971581
|
G | T | 1 | a0001c0003t0002g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.379-4134G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971581 | ||||||
| chr14:69971733
|
A | C | 68 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0108others(65): Show | 70 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.379-3982A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971733 | ||||||
| chr14:69971775
|
G | T | 1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.379-3940G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971775 | ||||||
| chr14:69971854
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG01074.hp2 HG01175.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.379-3861G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971854 | ||||||
| chr14:69971920
|
T | C | 8 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0031g0053others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-3795T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69971920 | ||||||
| chr14:69972065
|
C | T | 1 | a0001c0004t0005g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.379-3650C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972065 | ||||||
| chr14:69972131
|
G | C | 2 | a0001c0001t0001g0068a0006c0010t0001g0035 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.379-3584G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972131 | ||||||
| chr14:69972170
|
A | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0206others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-3545A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972170 | ||||||
| chr14:69972305
|
G | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-3410G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972305 | ||||||
| chr14:69972322
|
C | A | 44 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(41): Show | 44 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.379-3393C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972322 | ||||||
| chr14:69972412
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0031g0053a0006c0010t0001g0035 | 3 | HG01884.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.379-3303G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972412 | ||||||
| chr14:69972433
|
A | G | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-3282A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972433 | ||||||
| chr14:69972438
|
T | TG | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-3273dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 69972438 | |||||
| chr14:69972468
|
C | A | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 135 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.379-3247C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972468 | ||||||
| chr14:69972574
|
G | C | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-3141G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972574 | ||||||
| chr14:69972686
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0066others(18): Show | 22 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-3029G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69972686 | ||||||
| chr14:69973059
|
A | G | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-2656A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973059 | ||||||
| chr14:69973065
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(44): Show | 47 | HG01074.hp2 HG01106.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.379-2650G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973065 | ||||||
| chr14:69973124
|
T | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-2591T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973124 | ||||||
| chr14:69973139
|
C | G | 78 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055others(75): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.379-2576C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973139 | ||||||
| chr14:69973211
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-2504T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973211 | ||||||
| chr14:69973240
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(43): Show | 47 | HG01074.hp2 HG01106.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.379-2475C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973240 | ||||||
| chr14:69973364
|
T | C | 94 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0050others(91): Show | 95 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.379-2351T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973364 | ||||||
| chr14:69973440
|
A | T | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2275A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973440 | ||||||
| chr14:69973477
|
A | C | 2 | a0001c0001t0001g0203a0001c0001t0002g0157 | 2 | HG00558.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.379-2238A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973477 | ||||||
| chr14:69973493
|
G | C | 34 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055others(31): Show | 35 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.379-2222G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973493 | ||||||
| chr14:69973630
|
G | A | 1 | a0001c0001t0020g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.379-2085G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973630 | ||||||
| chr14:69973647
|
G | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 68 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.379-2068G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973647 | ||||||
| chr14:69973885
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0071others(15): Show | 19 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.379-1830G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973885 | ||||||
| chr14:69973958
|
T | A | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.379-1757T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69973958 | ||||||
| chr14:69974292
|
A | C | 1 | a0001c0003t0002g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.379-1423A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974292 | ||||||
| chr14:69974357
|
A | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(13): Show | 17 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.379-1358A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974357 | ||||||
| chr14:69974591
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.379-1124C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974591 | ||||||
| chr14:69974671
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0066others(18): Show | 22 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-1044G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974671 | ||||||
| chr14:69974687
|
T | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0066others(18): Show | 22 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-1028T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974687 | ||||||
| chr14:69974844
|
C | G | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-871C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974844 | ||||||
| chr14:69974960
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.379-755A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69974960 | ||||||
| chr14:69975167
|
A | C | 1 | a0001c0001t0029g0021 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.379-548A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975167 | ||||||
| chr14:69975247
|
G | A | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-468G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975247 | ||||||
| chr14:69975357
|
T | G | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-358T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975357 | ||||||
| chr14:69975365
|
T | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-350T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975365 | ||||||
| chr14:69975402
|
A | G | 1 | a0001c0002t0002g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.379-313A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975402 | ||||||
| chr14:69975512
|
C | T | 1 | a0001c0001t0020g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.379-203C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975512 | ||||||
| chr14:69975513
|
G | T | 28 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055others(25): Show | 28 | HG00140.hp1 HG00323.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.379-202G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975513 | ||||||
| chr14:69975624
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379-91G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975624 | ||||||
| chr14:69975633
|
A | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.379-82A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 3/11 | chr14 | 69975633 | ||||||
| chr14:69975831
|
C | T | 2 | a0001c0002t0002g0245a0001c0002t0002g0248 | 2 | NA18981.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.478+17C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69975831 | ||||||
| chr14:69975940
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.478+126A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69975940 | ||||||
| chr14:69976019
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(2): Show | 5 | NA18940.hp2 NA18956.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+205G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976019 | ||||||
| chr14:69976230
|
C | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.478+416C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976230 | ||||||
| chr14:69976270
|
A | G | 20 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0159others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.478+456A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976270 | ||||||
| chr14:69976369
|
C | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+555C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976369 | ||||||
| chr14:69976511
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+697T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976511 | ||||||
| chr14:69976623
|
A | G | 57 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(54): Show | 58 | HG00323.hp1 HG01074.hp2 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.478+809A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976623 | ||||||
| chr14:69976801
|
A | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+987A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976801 | ||||||
| chr14:69976817
|
G | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.478+1003G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69976817 | ||||||
| chr14:69977005
|
G | T | 5 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0006g0230others(2): Show | 6 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-913G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977005 | ||||||
| chr14:69977095
|
A | G | 1 | a0001c0004t0006g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.479-823A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977095 | ||||||
| chr14:69977102
|
G | A | 2 | a0001c0001t0005g0010a0001c0001t0005g0239 | 2 | HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.479-816G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977102 | ||||||
| chr14:69977117
|
C | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.479-801C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977117 | ||||||
| chr14:69977135
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0179a0001c0001t0001g0231others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-783G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977135 | ||||||
| chr14:69977368
|
T | C | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(150): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.479-550T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977368 | ||||||
| chr14:69977475
|
C | T | 2 | a0001c0001t0007g0095a0001c0007t0003g0008 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.479-443C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977475 | ||||||
| chr14:69977574
|
G | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0083others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.479-344G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977574 | ||||||
| chr14:69977589
|
G | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-329G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977589 | ||||||
| chr14:69977831
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.479-87A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977831 | ||||||
| chr14:69977906
|
T | G | 1 | a0001c0002t0025g0240 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.479-12T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 4/11 | chr14 | 69977906 | ||||||
| chr14:69978051
|
G | A | 3 | a0001c0001t0007g0097a0001c0001t0007g0100a0001c0001t0007g0102 | 3 | HG02818.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.526+86G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978051 | ||||||
| chr14:69978216
|
T | G | 1 | a0001c0001t0015g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.526+251T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978216 | ||||||
| chr14:69978368
|
C | A | 1 | a0001c0001t0004g0261 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.526+403C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978368 | ||||||
| chr14:69978389
|
A | G | 26 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG01106.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.526+424A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978389 | ||||||
| chr14:69978550
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0004g0047 | 2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.526+585G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978550 | ||||||
| chr14:69978797
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.526+832C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978797 | ||||||
| chr14:69978809
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.526+844A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69978809 | ||||||
| chr14:69979123
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.526+1158A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979123 | ||||||
| chr14:69979229
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.526+1264G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979229 | ||||||
| chr14:69979334
|
C | T | 23 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0063others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+1369C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979334 | ||||||
| chr14:69979604
|
G | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0083others(7): Show | 11 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+1639G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979604 | ||||||
| chr14:69979606
|
GT | G | 4 | a0001c0001t0004g0013a0001c0001t0004g0015a0001c0001t0004g0177others(1): Show | 4 | NA18949.hp1 NA18989.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1643delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69979606 | |||||
| chr14:69979608
|
TG | T | 3 | a0001c0001t0001g0235a0001c0004t0006g0201a0001c0004t0006g0202 | 3 | HG01081.hp2 HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526+1644delG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979608 | ||||||
| chr14:69979704
|
A | G | 45 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(42): Show | 45 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.526+1739A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69979704 | ||||||
| chr14:69980093
|
GTTTACAG others(26): Show |
G | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.526+2140_526+2172d others(35): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69980093 | |||||
| chr14:69980347
|
C | T | 3 | a0001c0001t0009g0037a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG01243.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.526+2382C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980347 | ||||||
| chr14:69980463
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0126others(4): Show | 7 | HG01433.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+2498C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980463 | ||||||
| chr14:69980542
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0168 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.526+2577G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980542 | ||||||
| chr14:69980727
|
C | T | 1 | a0001c0004t0005g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.526+2762C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980727 | ||||||
| chr14:69980765
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526+2800G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980765 | ||||||
| chr14:69980804
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.526+2839A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980804 | ||||||
| chr14:69980905
|
C | T | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.526+2940C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980905 | ||||||
| chr14:69980909
|
C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(60): Show | 64 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.526+2944C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980909 | ||||||
| chr14:69980946
|
C | T | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526+2981C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980946 | ||||||
| chr14:69980961
|
C | T | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.526+2996C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69980961 | ||||||
| chr14:69981047
|
GAAGGAGA others(8): Show |
G | 1 | a0001c0001t0006g0210 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.526+3087_526+3101d others(17): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69981047 | |||||
| chr14:69981221
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(25): Show | 28 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.526+3256G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981221 | ||||||
| chr14:69981232
|
A | AGG | 26 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG01106.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.526+3271_526+3272d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69981232 | |||||
| chr14:69981549
|
C | T | 45 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(42): Show | 45 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.526+3584C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981549 | ||||||
| chr14:69981673
|
G | A | 26 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG01106.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.526+3708G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981673 | ||||||
| chr14:69981719
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.526+3754A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981719 | ||||||
| chr14:69981941
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.526+3976A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981941 | ||||||
| chr14:69981973
|
A | C | 1 | a0001c0003t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.526+4008A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69981973 | ||||||
| chr14:69982148
|
T | C | 25 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+4183T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982148 | ||||||
| chr14:69982190
|
C | T | 56 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0041others(53): Show | 56 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.526+4225C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982190 | ||||||
| chr14:69982601
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.526+4636A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982601 | ||||||
| chr14:69982640
|
C | A | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.526+4675C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982640 | ||||||
| chr14:69982719
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.526+4754C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982719 | ||||||
| chr14:69982731
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0006g0080others(3): Show | 7 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+4766C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982731 | ||||||
| chr14:69982958
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(36): Show | 39 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.526+4993C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982958 | ||||||
| chr14:69982971
|
C | T | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.526+5006C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982971 | ||||||
| chr14:69982985
|
T | C | 2 | a0001c0002t0002g0012a0001c0002t0002g0183 | 2 | HG00438.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.526+5020T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982985 | ||||||
| chr14:69982989
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.526+5024T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69982989 | ||||||
| chr14:69983051
|
T | C | 1 | a0001c0001t0007g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.526+5086T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983051 | ||||||
| chr14:69983082
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0074others(6): Show | 9 | HG01433.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+5117G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983082 | ||||||
| chr14:69983108
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0226 | 2 | HG00438.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.526+5143G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983108 | ||||||
| chr14:69983305
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(19): Show | 22 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.526+5340C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983305 | ||||||
| chr14:69983315
|
T | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0041others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+5350T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983315 | ||||||
| chr14:69983367
|
G | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+5402G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983367 | ||||||
| chr14:69983453
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.526+5488A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983453 | ||||||
| chr14:69983462
|
G | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.526+5497G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983462 | ||||||
| chr14:69983502
|
G | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(66): Show | 71 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.526+5537G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983502 | ||||||
| chr14:69983579
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0026g0072 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.526+5614G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983579 | ||||||
| chr14:69983654
|
C | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0041others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+5689C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983654 | ||||||
| chr14:69983743
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.526+5778T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69983743 | ||||||
| chr14:69984004
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+6039G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984004 | ||||||
| chr14:69984023
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.526+6058A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984023 | ||||||
| chr14:69984119
|
T | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+6154T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984119 | ||||||
| chr14:69984131
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(63): Show | 67 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.526+6166G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984131 | ||||||
| chr14:69984178
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.526+6213A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984178 | ||||||
| chr14:69984191
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.526+6226A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984191 | ||||||
| chr14:69984420
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(19): Show | 22 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.526+6455G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984420 | ||||||
| chr14:69984475
|
G | A | 1 | a0001c0001t0015g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.526+6510G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984475 | ||||||
| chr14:69984680
|
TA | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.526+6732delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69984680 | |||||
| chr14:69984699
|
A | G | 1 | a0001c0001t0006g0230 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.526+6734A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984699 | ||||||
| chr14:69984728
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.526+6763G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984728 | ||||||
| chr14:69984756
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.526+6791G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984756 | ||||||
| chr14:69984813
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.526+6848C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984813 | ||||||
| chr14:69984819
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.526+6854T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984819 | ||||||
| chr14:69984855
|
TCAAA | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0084others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+6915_526+6918d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69984855 | |||||
| chr14:69984914
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.526+6949C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984914 | ||||||
| chr14:69984915
|
A | C | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.526+6950A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984915 | ||||||
| chr14:69984971
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(19): Show | 22 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.526+7006G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984971 | ||||||
| chr14:69984971
|
G | T | 1 | a0001c0002t0002g0256 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.526+7006G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69984971 | ||||||
| chr14:69985025
|
C | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0231 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.526+7060C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985025 | ||||||
| chr14:69985041
|
GA | G | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(90): Show | 94 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.526+7088delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69985041 | |||||
| chr14:69985063
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.526+7098G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985063 | ||||||
| chr14:69985106
|
A | G | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+7141A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985106 | ||||||
| chr14:69985207
|
CTATT | C | 15 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0087others(12): Show | 15 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-7209_527-7206d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985207 | ||||||
| chr14:69985487
|
G | GA | 30 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(27): Show | 30 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.527-6922dupA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69985487 | |||||
| chr14:69985521
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0110others(5): Show | 9 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-6896A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985521 | ||||||
| chr14:69985649
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.527-6768A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985649 | ||||||
| chr14:69985807
|
TGAGA | T | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-6607_527-6604d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69985807 | |||||
| chr14:69985832
|
C | A | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.527-6585C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985832 | ||||||
| chr14:69985897
|
C | T | 162 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.527-6520C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69985897 | ||||||
| chr14:69986212
|
A | G | 1 | a0001c0004t0005g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.527-6205A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986212 | ||||||
| chr14:69986498
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0125a0001c0001t0001g0206others(7): Show | 10 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.527-5919G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986498 | ||||||
| chr14:69986515
|
T | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-5902T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986515 | ||||||
| chr14:69986586
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.527-5831T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986586 | ||||||
| chr14:69986603
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.527-5814C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986603 | ||||||
| chr14:69986890
|
C | G | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.527-5527C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986890 | ||||||
| chr14:69986962
|
G | A | 44 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(41): Show | 44 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.527-5455G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69986962 | ||||||
| chr14:69987104
|
T | A | 4 | a0001c0001t0007g0032a0001c0001t0007g0034a0001c0007t0001g0124others(1): Show | 4 | HG02055.hp1 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-5313T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987104 | ||||||
| chr14:69987104
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.527-5313T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987104 | ||||||
| chr14:69987181
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0026g0072 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.527-5236G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987181 | ||||||
| chr14:69987263
|
A | G | 6 | a0001c0001t0001g0211a0001c0001t0001g0226a0001c0001t0001g0243others(3): Show | 6 | HG00438.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-5154A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987263 | ||||||
| chr14:69987327
|
C | A | 1 | a0001c0004t0004g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.527-5090C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987327 | ||||||
| chr14:69987437
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0015g0054a0001c0001t0015g0153others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-4980C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987437 | ||||||
| chr14:69987516
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0006g0109 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.527-4901A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987516 | ||||||
| chr14:69987555
|
G | A | 52 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(49): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.527-4862G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987555 | ||||||
| chr14:69987788
|
A | G | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-4629A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987788 | ||||||
| chr14:69987820
|
G | C | 1 | a0001c0005t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.527-4597G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987820 | ||||||
| chr14:69987953
|
C | G | 27 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 27 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.527-4464C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69987953 | ||||||
| chr14:69988016
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.527-4401G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988016 | ||||||
| chr14:69988067
|
T | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0087others(12): Show | 15 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-4350T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988067 | ||||||
| chr14:69988084
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.527-4333C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988084 | ||||||
| chr14:69988167
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.527-4250C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988167 | ||||||
| chr14:69988254
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.527-4163C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988254 | ||||||
| chr14:69988289
|
C | CT | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(63): Show | 67 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.527-4117dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69988289 | |||||
| chr14:69988289
|
C | CTT | 9 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(6): Show | 9 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-4118_527-4117d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69988289 | |||||
| chr14:69988289
|
C | CTTT | 47 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0127others(44): Show | 47 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.527-4119_527-4117d others(5): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69988289 | |||||
| chr14:69988289
|
CT | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(38): Show | 43 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.527-4117delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 69988289 | |||||
| chr14:69988302
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.527-4115A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988302 | ||||||
| chr14:69988530
|
C | T | 1 | a0001c0003t0002g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527-3887C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988530 | ||||||
| chr14:69988750
|
G | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(30): Show | 34 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.527-3667G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988750 | ||||||
| chr14:69988771
|
A | G | 44 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(41): Show | 44 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.527-3646A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988771 | ||||||
| chr14:69988806
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.527-3611G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69988806 | ||||||
| chr14:69989822
|
T | C | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.527-2595T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69989822 | ||||||
| chr14:69989899
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.527-2518G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69989899 | ||||||
| chr14:69989909
|
G | A | 12 | a0001c0001t0002g0181a0001c0001t0002g0207a0001c0001t0003g0056others(9): Show | 12 | HG00140.hp1 HG00323.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-2508G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69989909 | ||||||
| chr14:69989947
|
G | T | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.527-2470G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69989947 | ||||||
| chr14:69989982
|
T | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.527-2435T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69989982 | ||||||
| chr14:69990087
|
A | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.527-2330A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990087 | ||||||
| chr14:69990353
|
T | C | 10 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(7): Show | 11 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-2064T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990353 | ||||||
| chr14:69990405
|
G | A | 1 | a0001c0002t0025g0240 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.527-2012G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990405 | ||||||
| chr14:69990412
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.527-2005T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990412 | ||||||
| chr14:69990494
|
G | A | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527-1923G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990494 | ||||||
| chr14:69990639
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.527-1778A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990639 | ||||||
| chr14:69990927
|
A | G | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.527-1490A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990927 | ||||||
| chr14:69990936
|
A | C | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.527-1481A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990936 | ||||||
| chr14:69990974
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(27): Show | 30 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.527-1443T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69990974 | ||||||
| chr14:69991153
|
T | C | 1 | a0001c0001t0008g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.527-1264T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991153 | ||||||
| chr14:69991318
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(58): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.527-1099C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991318 | ||||||
| chr14:69991320
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.527-1097C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991320 | ||||||
| chr14:69991534
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(58): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.527-883A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991534 | ||||||
| chr14:69991649
|
C | G | 2 | a0001c0004t0006g0201a0001c0004t0006g0202 | 2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527-768C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991649 | ||||||
| chr14:69991657
|
C | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-760C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991657 | ||||||
| chr14:69991742
|
A | G | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527-675A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991742 | ||||||
| chr14:69991911
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.527-506A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991911 | ||||||
| chr14:69991967
|
G | A | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-450G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69991967 | ||||||
| chr14:69992038
|
G | C | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.527-379G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992038 | ||||||
| chr14:69992054
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-363A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992054 | ||||||
| chr14:69992066
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.527-351T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992066 | ||||||
| chr14:69992079
|
C | T | 1 | a0004c0012t0001g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.527-338C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992079 | ||||||
| chr14:69992104
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(8): Show | 12 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-313C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992104 | ||||||
| chr14:69992149
|
C | T | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.527-268C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992149 | ||||||
| chr14:69992183
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(19): Show | 22 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.527-234C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992183 | ||||||
| chr14:69992318
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.527-99C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 5/11 | chr14 | 69992318 | ||||||
| chr14:69992653
|
T | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.583+180T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69992653 | ||||||
| chr14:69992782
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.583+309A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69992782 | ||||||
| chr14:69992870
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0087others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.583+397G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69992870 | ||||||
| chr14:69992995
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(58): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.583+522C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69992995 | ||||||
| chr14:69993011
|
GC | G | 5 | a0001c0001t0001g0071a0001c0001t0015g0054a0001c0001t0015g0153others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.583+539delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993011 | ||||||
| chr14:69993076
|
A | G | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.583+603A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993076 | ||||||
| chr14:69993083
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0005g0219others(1): Show | 4 | HG01175.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+610G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993083 | ||||||
| chr14:69993188
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.583+715G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993188 | ||||||
| chr14:69993314
|
G | A | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.583+841G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993314 | ||||||
| chr14:69993394
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.583+921T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993394 | ||||||
| chr14:69993401
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0091 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.583+928T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993401 | ||||||
| chr14:69993490
|
A | T | 1 | a0001c0001t0005g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.584-910A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993490 | ||||||
| chr14:69993551
|
G | T | 2 | a0001c0007t0001g0124a0001c0007t0003g0008 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.584-849G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993551 | ||||||
| chr14:69993611
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-789T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993611 | ||||||
| chr14:69993718
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0074others(5): Show | 8 | HG01433.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.584-682A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993718 | ||||||
| chr14:69993837
|
T | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.584-563T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993837 | ||||||
| chr14:69993838
|
C | T | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-562C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993838 | ||||||
| chr14:69993891
|
T | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.584-509T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993891 | ||||||
| chr14:69993892
|
T | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.584-508T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993892 | ||||||
| chr14:69993914
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0028others(36): Show | 40 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.584-486C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993914 | ||||||
| chr14:69993937
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0127others(8): Show | 12 | HG01496.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.584-463G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993937 | ||||||
| chr14:69993976
|
C | T | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.584-424C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993976 | ||||||
| chr14:69993978
|
T | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0087others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.584-422T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993978 | ||||||
| chr14:69993999
|
G | A | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.584-401G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69993999 | ||||||
| chr14:69994033
|
C | T | 1 | a0003c0009t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.584-367C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69994033 | ||||||
| chr14:69994034
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.584-366G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69994034 | ||||||
| chr14:69994252
|
G | A | 4 | a0001c0005t0001g0033a0001c0005t0001g0040a0001c0005t0001g0069others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-148G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69994252 | ||||||
| chr14:69994296
|
T | C | 1 | a0001c0002t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.584-104T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 6/11 | chr14 | 69994296 | ||||||
| chr14:69994601
|
A | G | 1 | a0001c0001t0008g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.664+121A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994601 | ||||||
| chr14:69994658
|
A | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(3): Show | 6 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+178A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994658 | ||||||
| chr14:69994720
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.664+240G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994720 | ||||||
| chr14:69994850
|
G | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.664+370G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994850 | ||||||
| chr14:69994856
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+376A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994856 | ||||||
| chr14:69994874
|
G | A | 1 | a0001c0003t0002g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.664+394G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69994874 | ||||||
| chr14:69995011
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664+531C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995011 | ||||||
| chr14:69995075
|
T | C | 1 | a0006c0010t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.664+595T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995075 | ||||||
| chr14:69995337
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0128 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.664+857C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995337 | ||||||
| chr14:69995377
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.664+897G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995377 | ||||||
| chr14:69995402
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(5): Show | 9 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.664+922G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995402 | ||||||
| chr14:69995499
|
C | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(4): Show | 7 | HG01106.hp1 HG02622.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+1019C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995499 | ||||||
| chr14:69995535
|
G | A | 2 | a0001c0001t0001g0098a0002c0013t0023g0027 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.664+1055G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995535 | ||||||
| chr14:69995644
|
C | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.664+1164C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69995644 | ||||||
| chr14:69996346
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1866A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996346 | ||||||
| chr14:69996387
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.664+1907A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996387 | ||||||
| chr14:69996463
|
C | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.664+1983C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996463 | ||||||
| chr14:69996530
|
C | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 32 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.664+2050C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996530 | ||||||
| chr14:69996777
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.664+2297A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996777 | ||||||
| chr14:69996779
|
T | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0231 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.664+2299T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996779 | ||||||
| chr14:69996971
|
T | C | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.664+2491T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996971 | ||||||
| chr14:69996972
|
G | A | 1 | a0001c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.664+2492G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69996972 | ||||||
| chr14:69997209
|
A | T | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.664+2729A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997209 | ||||||
| chr14:69997245
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.664+2765C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997245 | ||||||
| chr14:69997350
|
G | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.664+2870G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997350 | ||||||
| chr14:69997422
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+2942G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997422 | ||||||
| chr14:69997440
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.664+2960C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997440 | ||||||
| chr14:69997807
|
A | G | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.664+3327A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997807 | ||||||
| chr14:69997886
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(8): Show | 12 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+3406G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997886 | ||||||
| chr14:69997986
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0048others(28): Show | 32 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.664+3506T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997986 | ||||||
| chr14:69997991
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.664+3511C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69997991 | ||||||
| chr14:69998049
|
G | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(8): Show | 12 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+3569G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998049 | ||||||
| chr14:69998136
|
G | T | 1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.664+3656G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998136 | ||||||
| chr14:69998211
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.664+3731T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998211 | ||||||
| chr14:69998428
|
G | GT | 72 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0055others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.664+3962dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 69998428 | |||||
| chr14:69998527
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.664+4047A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998527 | ||||||
| chr14:69998666
|
T | C | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.664+4186T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998666 | ||||||
| chr14:69998786
|
G | A | 2 | a0001c0001t0007g0032a0001c0001t0007g0034 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.664+4306G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998786 | ||||||
| chr14:69998806
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+4326G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998806 | ||||||
| chr14:69998985
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0046others(28): Show | 32 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.664+4505T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69998985 | ||||||
| chr14:69999284
|
T | TG | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0046others(28): Show | 32 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.664+4808dupG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 69999284 | |||||
| chr14:69999303
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.664+4823G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999303 | ||||||
| chr14:69999331
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+4851C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999331 | ||||||
| chr14:69999364
|
C | T | 20 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 20 | HG00642.hp1 HG01167.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.664+4884C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999364 | ||||||
| chr14:69999428
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.664+4948T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999428 | ||||||
| chr14:69999430
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0015g0054a0001c0001t0015g0153others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+4950G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999430 | ||||||
| chr14:69999442
|
C | T | 1 | a0001c0001t0007g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.664+4962C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999442 | ||||||
| chr14:69999468
|
T | C | 2 | a0001c0002t0002g0023a0001c0002t0002g0212 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.664+4988T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999468 | ||||||
| chr14:69999533
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0049 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.664+5053G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999533 | ||||||
| chr14:69999647
|
T | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0052others(9): Show | 12 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.664+5167T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999647 | ||||||
| chr14:69999843
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG00639.hp2 HG01167.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664+5363C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999843 | ||||||
| chr14:69999970
|
C | CT | 12 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(9): Show | 13 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+5495dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 69999970 | |||||
| chr14:69999987
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.664+5507G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 69999987 | ||||||
| chr14:70000080
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.664+5600C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000080 | ||||||
| chr14:70000170
|
G | T | 9 | a0001c0001t0001g0052a0001c0001t0001g0084a0001c0001t0001g0126others(6): Show | 9 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.664+5690G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000170 | ||||||
| chr14:70000287
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.664+5807C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000287 | ||||||
| chr14:70000573
|
C | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0046others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.664+6093C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000573 | ||||||
| chr14:70000640
|
A | G | 8 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0159others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+6160A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000640 | ||||||
| chr14:70000648
|
A | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0046others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.664+6168A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000648 | ||||||
| chr14:70000740
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.664+6260C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000740 | ||||||
| chr14:70000906
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.664+6426C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000906 | ||||||
| chr14:70000941
|
C | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0050others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.664+6461C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70000941 | ||||||
| chr14:70001225
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.664+6745G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70001225 | ||||||
| chr14:70001230
|
G | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0020others(105): Show | 111 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.664+6750G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70001230 | ||||||
| chr14:70001734
|
C | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.664+7254C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70001734 | ||||||
| chr14:70001819
|
C | T | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.664+7339C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70001819 | ||||||
| chr14:70001969
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.664+7489T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70001969 | ||||||
| chr14:70002069
|
C | T | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.664+7589C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002069 | ||||||
| chr14:70002083
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.664+7603T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002083 | ||||||
| chr14:70002137
|
A | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.664+7657A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002137 | ||||||
| chr14:70002191
|
G | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.664+7711G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002191 | ||||||
| chr14:70002223
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.664+7743A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002223 | ||||||
| chr14:70002321
|
T | A | 3 | a0001c0001t0001g0108a0001c0001t0002g0003a0004c0012t0001g0107 | 4 | HG01069.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+7841T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002321 | ||||||
| chr14:70002403
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.664+7923T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002403 | ||||||
| chr14:70002414
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.664+7934G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002414 | ||||||
| chr14:70002471
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.664+7991T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002471 | ||||||
| chr14:70002538
|
A | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.664+8058A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002538 | ||||||
| chr14:70002610
|
C | T | 1 | a0001c0002t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.664+8130C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002610 | ||||||
| chr14:70002643
|
T | A | 1 | a0001c0002t0001g0137 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.665-8111T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002643 | ||||||
| chr14:70002653
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0050 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.665-8101T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70002653 | ||||||
| chr14:70003044
|
C | T | 1 | a0001c0001t0029g0021 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.665-7710C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003044 | ||||||
| chr14:70003049
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0011g0075 | 2 | HG01175.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.665-7705G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003049 | ||||||
| chr14:70003110
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.665-7644T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003110 | ||||||
| chr14:70003188
|
A | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-7566A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003188 | ||||||
| chr14:70003266
|
A | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-7488A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003266 | ||||||
| chr14:70003286
|
A | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-7468A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003286 | ||||||
| chr14:70003465
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.665-7289C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003465 | ||||||
| chr14:70003567
|
C | T | 9 | a0001c0001t0001g0098a0001c0001t0001g0126a0001c0001t0001g0152others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.665-7187C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003567 | ||||||
| chr14:70003585
|
T | C | 2 | a0001c0003t0002g0141a0001c0003t0002g0171 | 2 | HG00558.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.665-7169T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003585 | ||||||
| chr14:70003616
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0110others(6): Show | 10 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.665-7138A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003616 | ||||||
| chr14:70003703
|
T | A | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-7051T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003703 | ||||||
| chr14:70003919
|
T | C | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.665-6835T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70003919 | ||||||
| chr14:70004083
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.665-6671T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004083 | ||||||
| chr14:70004156
|
T | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 19 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.665-6598T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004156 | ||||||
| chr14:70004224
|
G | A | 3 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0017g0176 | 3 | HG01109.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-6530G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004224 | ||||||
| chr14:70004438
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0127 | 3 | HG01496.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.665-6316G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004438 | ||||||
| chr14:70004482
|
T | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-6272T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004482 | ||||||
| chr14:70004495
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.665-6259A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004495 | ||||||
| chr14:70004559
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.665-6195C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004559 | ||||||
| chr14:70004564
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.665-6190C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004564 | ||||||
| chr14:70004750
|
G | T | 2 | a0001c0001t0001g0068a0006c0010t0001g0035 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.665-6004G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004750 | ||||||
| chr14:70004810
|
C | T | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.665-5944C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004810 | ||||||
| chr14:70004886
|
G | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-5868G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004886 | ||||||
| chr14:70004891
|
C | G | 2 | a0001c0003t0001g0167a0001c0003t0001g0182 | 2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.665-5863C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70004891 | ||||||
| chr14:70005130
|
A | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-5624A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70005130 | ||||||
| chr14:70005176
|
AAAAG | A | 5 | a0001c0001t0001g0071a0001c0001t0015g0054a0001c0001t0015g0153others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-5575_665-5572d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 70005176 | |||||
| chr14:70005456
|
T | C | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-5298T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70005456 | ||||||
| chr14:70005694
|
A | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 19 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.665-5060A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70005694 | ||||||
| chr14:70005770
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.665-4984G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70005770 | ||||||
| chr14:70005841
|
G | A | 2 | a0001c0001t0014g0106a0001c0001t0014g0173 | 2 | HG01168.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.665-4913G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70005841 | ||||||
| chr14:70006004
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(8): Show | 12 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.665-4750T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006004 | ||||||
| chr14:70006095
|
C | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0020others(107): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.665-4659C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006095 | ||||||
| chr14:70006218
|
T | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-4536T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006218 | ||||||
| chr14:70006221
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0015g0054a0001c0001t0015g0153others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-4533C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006221 | ||||||
| chr14:70006648
|
C | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.665-4106C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006648 | ||||||
| chr14:70006735
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.665-4019C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006735 | ||||||
| chr14:70006781
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.665-3973C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006781 | ||||||
| chr14:70006983
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.665-3771G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70006983 | ||||||
| chr14:70007138
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.665-3616C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007138 | ||||||
| chr14:70007261
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0009g0037a0001c0001t0009g0038others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3493C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007261 | ||||||
| chr14:70007291
|
C | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0020others(72): Show | 77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.665-3463C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007291 | ||||||
| chr14:70007300
|
C | T | 1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.665-3454C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007300 | ||||||
| chr14:70007451
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.665-3303G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007451 | ||||||
| chr14:70007490
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0020others(107): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.665-3264G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007490 | ||||||
| chr14:70007725
|
A | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 19 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.665-3029A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007725 | ||||||
| chr14:70007817
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665-2937C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007817 | ||||||
| chr14:70007896
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.665-2858A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007896 | ||||||
| chr14:70007949
|
C | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.665-2805C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70007949 | ||||||
| chr14:70008101
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0127 | 3 | HG01496.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.665-2653G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008101 | ||||||
| chr14:70008117
|
A | ATTATT | 18 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 19 | HG01074.hp2 HG01433.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.665-2611_665-2607d others(7): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 70008117 | |||||
| chr14:70008117
|
A | ATTATTTT others(3): Show |
1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.665-2616_665-2607d others(12): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 70008117 | |||||
| chr14:70008117
|
ATTATT | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0073 | 2 | HG01496.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.665-2611_665-2607d others(7): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 70008117 | |||||
| chr14:70008190
|
C | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0125others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.665-2564C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008190 | ||||||
| chr14:70008191
|
G | A | 26 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 26 | HG00642.hp1 HG01167.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.665-2563G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008191 | ||||||
| chr14:70008193
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG01074.hp2 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-2561G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008193 | ||||||
| chr14:70008266
|
A | T | 2 | a0001c0003t0001g0167a0001c0003t0001g0182 | 2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.665-2488A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008266 | ||||||
| chr14:70008330
|
T | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0020others(107): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.665-2424T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008330 | ||||||
| chr14:70008393
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(5): Show | 8 | HG03704.hp1 HG04228.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-2361C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008393 | ||||||
| chr14:70008409
|
G | A | 2 | a0001c0001t0007g0097a0001c0001t0007g0100 | 2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.665-2345G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008409 | ||||||
| chr14:70008669
|
C | G | 1 | a0001c0003t0004g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.665-2085C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008669 | ||||||
| chr14:70008686
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.665-2068T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008686 | ||||||
| chr14:70008779
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.665-1975C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008779 | ||||||
| chr14:70008792
|
C | T | 2 | a0001c0003t0001g0167a0001c0003t0001g0182 | 2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.665-1962C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008792 | ||||||
| chr14:70008797
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665-1957A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008797 | ||||||
| chr14:70008981
|
G | C | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1773G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008981 | ||||||
| chr14:70008990
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-1764T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70008990 | ||||||
| chr14:70009038
|
A | AG | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-1716_665-1715i others(3): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009038 | ||||||
| chr14:70009041
|
A | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-1713A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009041 | ||||||
| chr14:70009097
|
C | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-1657C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009097 | ||||||
| chr14:70009101
|
G | A | 1 | a0001c0001t0003g0016 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.665-1653G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009101 | ||||||
| chr14:70009409
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.665-1345C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009409 | ||||||
| chr14:70009493
|
A | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-1261A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009493 | ||||||
| chr14:70009609
|
A | C | 4 | a0001c0001t0015g0054a0001c0001t0015g0153a0001c0001t0016g0078others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-1145A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009609 | ||||||
| chr14:70009626
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.665-1128G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009626 | ||||||
| chr14:70009734
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.665-1020C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009734 | ||||||
| chr14:70009954
|
T | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.665-800T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009954 | ||||||
| chr14:70009961
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.665-793C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70009961 | ||||||
| chr14:70010228
|
G | A | 8 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-526G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70010228 | ||||||
| chr14:70010271
|
T | C | 10 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0264others(7): Show | 11 | HG00323.hp2 HG01069.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-483T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70010271 | ||||||
| chr14:70010305
|
G | T | 127 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(124): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.665-449G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70010305 | ||||||
| chr14:70010549
|
G | A | 3 | a0001c0001t0007g0032a0001c0001t0007g0034a0001c0001t0007g0095 | 3 | HG02055.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.665-205G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 7/11 | chr14 | 70010549 | ||||||
| chr14:70010978
|
C | T | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.857+32C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70010978 | ||||||
| chr14:70011069
|
A | G | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.857+123A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70011069 | ||||||
| chr14:70011225
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.858-260G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70011225 | ||||||
| chr14:70011344
|
C | T | 3 | a0001c0001t0007g0032a0001c0001t0007g0034a0001c0001t0007g0095 | 3 | HG02055.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.858-141C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70011344 | ||||||
| chr14:70011456
|
CA | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.858-27delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 70011456 | |||||
| chr14:70011459
|
C | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.858-26C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70011459 | ||||||
| chr14:70011466
|
C | A | 46 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0001g0257others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.858-19C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 8/11 | chr14 | 70011466 | ||||||
| chr14:70011594
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0073 | 2 | HG01496.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.940+27G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70011594 | ||||||
| chr14:70011744
|
A | C | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.940+177A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70011744 | ||||||
| chr14:70011783
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.940+216G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70011783 | ||||||
| chr14:70011960
|
G | A | 2 | a0001c0002t0001g0257a0001c0002t0002g0129 | 2 | NA18953.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.940+393G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70011960 | ||||||
| chr14:70011989
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.940+422C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70011989 | ||||||
| chr14:70012127
|
T | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.940+560T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012127 | ||||||
| chr14:70012172
|
G | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0152a0001c0001t0001g0154others(4): Show | 7 | HG01109.hp2 HG01433.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+605G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012172 | ||||||
| chr14:70012230
|
A | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.940+663A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012230 | ||||||
| chr14:70012361
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0010g0099 | 2 | HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.940+794C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012361 | ||||||
| chr14:70012440
|
A | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.940+873A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012440 | ||||||
| chr14:70012457
|
T | C | 136 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(133): Show | 139 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.940+890T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012457 | ||||||
| chr14:70012541
|
A | G | 2 | a0001c0001t0001g0126a0002c0013t0023g0027 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.941-845A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012541 | ||||||
| chr14:70012753
|
C | T | 30 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(27): Show | 30 | HG00642.hp1 HG01167.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.941-633C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012753 | ||||||
| chr14:70012806
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0264 | 2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.941-580G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012806 | ||||||
| chr14:70012939
|
A | G | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.941-447A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012939 | ||||||
| chr14:70012987
|
T | G | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.941-399T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 9/11 | chr14 | 70012987 | ||||||
| chr14:70013498
|
T | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(59): Show | 62 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.1046+7T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70013498 | ||||||
| chr14:70013529
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1046+38T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70013529 | ||||||
| chr14:70013564
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1046+73G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70013564 | ||||||
| chr14:70013585
|
G | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG01074.hp2 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046+94G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70013585 | ||||||
| chr14:70013898
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1046+407G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70013898 | ||||||
| chr14:70014391
|
T | G | 4 | a0001c0005t0001g0033a0001c0005t0001g0040a0001c0005t0001g0069others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+900T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70014391 | ||||||
| chr14:70014781
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1046+1290G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70014781 | ||||||
| chr14:70014781
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0083 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1046+1290G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70014781 | ||||||
| chr14:70014792
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01074.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1046+1301G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70014792 | ||||||
| chr14:70014868
|
G | A | 11 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0125others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+1377G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70014868 | ||||||
| chr14:70015215
|
C | T | 45 | a0001c0002t0001g0117a0001c0002t0001g0137a0001c0002t0002g0012others(42): Show | 45 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1046+1724C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015215 | ||||||
| chr14:70015461
|
CA | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1046+1980delA | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70015461 | |||||
| chr14:70015464
|
A | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0216a0001c0001t0014g0106others(1): Show | 4 | HG01168.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+1973A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015464 | ||||||
| chr14:70015544
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1046+2053C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015544 | ||||||
| chr14:70015563
|
G | A | 1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1046+2072G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015563 | ||||||
| chr14:70015619
|
G | T | 1 | a0001c0001t0020g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1046+2128G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015619 | ||||||
| chr14:70015712
|
G | A | 1 | a0001c0003t0004g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1046+2221G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015712 | ||||||
| chr14:70015716
|
T | C | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1046+2225T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015716 | ||||||
| chr14:70015740
|
C | T | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(4): Show | 7 | HG01081.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046+2249C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015740 | ||||||
| chr14:70015864
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1046+2373A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70015864 | ||||||
| chr14:70016060
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1046+2569T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016060 | ||||||
| chr14:70016406
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(49): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1046+2915C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016406 | ||||||
| chr14:70016559
|
A | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1046+3068A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016559 | ||||||
| chr14:70016656
|
C | T | 2 | a0001c0002t0002g0245a0001c0002t0002g0248 | 2 | NA18981.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1046+3165C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016656 | ||||||
| chr14:70016716
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1046+3225C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016716 | ||||||
| chr14:70016739
|
C | T | 1 | a0001c0001t0005g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1046+3248C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016739 | ||||||
| chr14:70016867
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+3376A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016867 | ||||||
| chr14:70016934
|
C | A | 1 | a0001c0001t0005g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1046+3443C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016934 | ||||||
| chr14:70016953
|
C | T | 11 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1046+3462C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016953 | ||||||
| chr14:70016990
|
G | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(8): Show | 12 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+3499G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70016990 | ||||||
| chr14:70017148
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0014g0106a0001c0001t0014g0173 | 3 | HG01168.hp1 HG03704.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1046+3657C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017148 | ||||||
| chr14:70017256
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0010g0099 | 3 | HG01192.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1046+3765G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017256 | ||||||
| chr14:70017296
|
C | T | 1 | a0001c0001t0033g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1046+3805C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017296 | ||||||
| chr14:70017297
|
G | A | 1 | a0001c0002t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1046+3806G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017297 | ||||||
| chr14:70017428
|
G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1046+3937G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017428 | ||||||
| chr14:70017849
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1046+4358G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70017849 | ||||||
| chr14:70018337
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0055others(2): Show | 5 | HG02970.hp2 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+4846G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018337 | ||||||
| chr14:70018364
|
TC | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(49): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-4836delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70018364 | |||||
| chr14:70018374
|
G | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0050others(26): Show | 31 | HG00323.hp2 HG01069.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1047-4829G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018374 | ||||||
| chr14:70018464
|
G | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(50): Show | 53 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1047-4739G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018464 | ||||||
| chr14:70018547
|
C | T | 2 | a0001c0001t0004g0047a0001c0004t0004g0105 | 2 | HG03927.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1047-4656C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018547 | ||||||
| chr14:70018697
|
C | A | 1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1047-4506C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018697 | ||||||
| chr14:70018714
|
A | G | 2 | a0001c0002t0002g0195a0001c0002t0028g0223 | 2 | NA19002.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1047-4489A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018714 | ||||||
| chr14:70018800
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0010g0099 | 3 | HG01192.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1047-4403C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70018800 | ||||||
| chr14:70019087
|
T | C | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(147): Show | 153 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1047-4116T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019087 | ||||||
| chr14:70019129
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0127 | 3 | HG01496.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1047-4074G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019129 | ||||||
| chr14:70019177
|
C | T | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1047-4026C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019177 | ||||||
| chr14:70019191
|
A | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0229a0001c0001t0001g0232 | 3 | HG01071.hp1 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1047-4012A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019191 | ||||||
| chr14:70019256
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(32): Show | 35 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1047-3947C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019256 | ||||||
| chr14:70019336
|
A | C | 1 | a0001c0002t0002g0180 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1047-3867A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019336 | ||||||
| chr14:70019815
|
G | C | 1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1047-3388G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019815 | ||||||
| chr14:70019825
|
T | C | 50 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0055others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1047-3378T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019825 | ||||||
| chr14:70019831
|
A | G | 20 | a0001c0001t0002g0207a0001c0001t0003g0016a0001c0001t0003g0056others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1047-3372A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019831 | ||||||
| chr14:70019932
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(11): Show | 15 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047-3271G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70019932 | ||||||
| chr14:70020025
|
T | C | 71 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0049others(68): Show | 72 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1047-3178T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020025 | ||||||
| chr14:70020053
|
ATCT | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(48): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-3142_1047-314 others(7): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70020053 | |||||
| chr14:70020097
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0146 | 2 | NA19005.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1047-3106T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020097 | ||||||
| chr14:70020148
|
T | C | 51 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0157others(48): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-3055T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020148 | ||||||
| chr14:70020151
|
C | CTT | 51 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0157others(48): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-3041_1047-304 others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70020151 | |||||
| chr14:70020151
|
CT | C | 22 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1047-3040delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70020151 | |||||
| chr14:70020527
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1047-2676G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020527 | ||||||
| chr14:70020562
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076 | 3 | HG02559.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1047-2641C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020562 | ||||||
| chr14:70020574
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(140): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1047-2629A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020574 | ||||||
| chr14:70020679
|
C | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0213others(7): Show | 10 | HG00323.hp2 HG01081.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1047-2524C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020679 | ||||||
| chr14:70020879
|
T | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 56 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1047-2324T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020879 | ||||||
| chr14:70020890
|
A | T | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-2313A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020890 | ||||||
| chr14:70020950
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1047-2253C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70020950 | ||||||
| chr14:70021015
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1047-2188G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021015 | ||||||
| chr14:70021022
|
T | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1047-2181T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021022 | ||||||
| chr14:70021046
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1047-2157C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021046 | ||||||
| chr14:70021062
|
C | A | 4 | a0001c0002t0002g0151a0001c0003t0002g0014a0001c0003t0002g0246others(1): Show | 4 | HG02015.hp2 HG02074.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-2141C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021062 | ||||||
| chr14:70021193
|
C | T | 12 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1047-2010C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021193 | ||||||
| chr14:70021288
|
T | C | 51 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0157others(48): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-1915T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021288 | ||||||
| chr14:70021291
|
A | C | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-1912A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021291 | ||||||
| chr14:70021302
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1047-1901A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021302 | ||||||
| chr14:70021369
|
T | C | 1 | a0001c0002t0002g0185 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1047-1834T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021369 | ||||||
| chr14:70021386
|
C | T | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-1817C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021386 | ||||||
| chr14:70021550
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1047-1653C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021550 | ||||||
| chr14:70021714
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1047-1489T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021714 | ||||||
| chr14:70021715
|
TC | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1482delC | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70021715 | |||||
| chr14:70021761
|
T | A | 51 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0157others(48): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1047-1442T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021761 | ||||||
| chr14:70021780
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1423G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021780 | ||||||
| chr14:70021805
|
G | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1398G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021805 | ||||||
| chr14:70021858
|
T | A | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-1345T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021858 | ||||||
| chr14:70021871
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0055others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047-1332A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021871 | ||||||
| chr14:70021930
|
C | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047-1273C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021930 | ||||||
| chr14:70021931
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1047-1272G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021931 | ||||||
| chr14:70021956
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0055others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047-1247A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70021956 | ||||||
| chr14:70022164
|
C | G | 65 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(62): Show | 66 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1047-1039C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022164 | ||||||
| chr14:70022333
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1047-870G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022333 | ||||||
| chr14:70022348
|
T | G | 1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1047-855T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022348 | ||||||
| chr14:70022393
|
AG | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047-808delG | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 70022393 | |||||
| chr14:70022533
|
C | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 66 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1047-670C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022533 | ||||||
| chr14:70022534
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1047-669G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022534 | ||||||
| chr14:70022587
|
C | T | 12 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0089others(9): Show | 12 | HG00140.hp1 HG00323.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1047-616C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022587 | ||||||
| chr14:70022664
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0216 | 2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1047-539A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022664 | ||||||
| chr14:70022754
|
A | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0181 | 2 | NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1047-449A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022754 | ||||||
| chr14:70022832
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1047-371G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022832 | ||||||
| chr14:70022887
|
A | G | 1 | a0001c0003t0002g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1047-316A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022887 | ||||||
| chr14:70022963
|
T | G | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1047-240T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70022963 | ||||||
| chr14:70023037
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0010g0099 | 3 | HG01192.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1047-166G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70023037 | ||||||
| chr14:70023058
|
C | G | 10 | a0001c0001t0001g0213a0001c0001t0001g0264a0001c0001t0006g0080others(7): Show | 10 | HG00323.hp2 HG01081.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1047-145C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70023058 | ||||||
| chr14:70023063
|
G | T | 1 | a0001c0001t0021g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1047-140G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 10/11 | chr14 | 70023063 | ||||||
| chr14:70023505
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1291+58G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023505 | ||||||
| chr14:70023547
|
A | G | 83 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0044others(80): Show | 85 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1291+100A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023547 | ||||||
| chr14:70023555
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1291+108A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023555 | ||||||
| chr14:70023655
|
A | C | 34 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0041others(31): Show | 34 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1291+208A>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023655 | ||||||
| chr14:70023717
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1291+270G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023717 | ||||||
| chr14:70023755
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1291+308G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023755 | ||||||
| chr14:70023783
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1291+336C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023783 | ||||||
| chr14:70023829
|
A | ATG | 13 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0074others(10): Show | 13 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291+408_1291+409d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70023829 | |||||
| chr14:70023829
|
ATG | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0134a0001c0001t0001g0213others(9): Show | 12 | HG00323.hp2 HG01081.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+408_1291+409d others(4): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70023829 | |||||
| chr14:70023829
|
ATGTG | A | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(10): Show | 13 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1291+406_1291+409d others(6): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70023829 | |||||
| chr14:70023862
|
T | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0074others(12): Show | 15 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1291+415T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023862 | ||||||
| chr14:70023914
|
G | A | 1 | a0001c0001t0018g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1291+467G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023914 | ||||||
| chr14:70023927
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1291+480A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023927 | ||||||
| chr14:70023962
|
G | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0044others(18): Show | 21 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1291+515G>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023962 | ||||||
| chr14:70023990
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1291+543G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70023990 | ||||||
| chr14:70024006
|
G | A | 1 | a0001c0001t0031g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1291+559G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024006 | ||||||
| chr14:70024082
|
G | A | 78 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0046others(75): Show | 80 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1291+635G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024082 | ||||||
| chr14:70024099
|
G | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1291+652G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024099 | ||||||
| chr14:70024172
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | NA18940.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1291+725G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024172 | ||||||
| chr14:70024316
|
A | G | 1 | a0001c0004t0005g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1291+869A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024316 | ||||||
| chr14:70024323
|
C | T | 1 | a0001c0001t0022g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1291+876C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024323 | ||||||
| chr14:70024324
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 51 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1291+877G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024324 | ||||||
| chr14:70024325
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1291+878A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024325 | ||||||
| chr14:70024472
|
G | A | 8 | a0001c0001t0001g0110a0001c0001t0001g0149a0001c0001t0001g0205others(5): Show | 8 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+1025G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024472 | ||||||
| chr14:70024474
|
A | G | 1 | a0001c0002t0002g0169 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1291+1027A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024474 | ||||||
| chr14:70024597
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1291+1150G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024597 | ||||||
| chr14:70024615
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0074others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1168A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024615 | ||||||
| chr14:70024643
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076 | 3 | HG02559.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1291+1196G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024643 | ||||||
| chr14:70024666
|
C | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0127others(8): Show | 11 | HG01496.hp2 HG02486.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+1219C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024666 | ||||||
| chr14:70024736
|
G | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(12): Show | 15 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1291+1289G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024736 | ||||||
| chr14:70024815
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(15): Show | 19 | HG00639.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1291+1368G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024815 | ||||||
| chr14:70024973
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0074others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1526A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70024973 | ||||||
| chr14:70025046
|
G | T | 55 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0090others(52): Show | 56 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1291+1599G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025046 | ||||||
| chr14:70025113
|
G | A | 7 | a0001c0002t0002g0012a0001c0002t0002g0164a0001c0002t0002g0183others(4): Show | 7 | HG00438.hp1 NA18942.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+1666G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025113 | ||||||
| chr14:70025291
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1291+1844C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025291 | ||||||
| chr14:70025308
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1291+1861A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025308 | ||||||
| chr14:70025389
|
C | A | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1291+1942C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025389 | ||||||
| chr14:70025536
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+2089A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025536 | ||||||
| chr14:70025566
|
C | T | 1 | a0005c0008t0002g0251 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1291+2119C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025566 | ||||||
| chr14:70025577
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076 | 3 | HG02559.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1291+2130T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025577 | ||||||
| chr14:70025735
|
A | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076 | 3 | HG02559.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1291+2288A>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70025735 | ||||||
| chr14:70026060
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+2613C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026060 | ||||||
| chr14:70026129
|
G | A | 77 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0044others(74): Show | 78 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1291+2682G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026129 | ||||||
| chr14:70026239
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0258 | 2 | NA18747.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1291+2792T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026239 | ||||||
| chr14:70026382
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1291+2935A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026382 | ||||||
| chr14:70026387
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1291+2940C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026387 | ||||||
| chr14:70026390
|
C | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0076 | 3 | HG02559.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1291+2943C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026390 | ||||||
| chr14:70026726
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+3279C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70026726 | ||||||
| chr14:70027037
|
A | G | 14 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0073others(11): Show | 14 | HG01496.hp2 HG02486.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-3205A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027037 | ||||||
| chr14:70027091
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-3151A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027091 | ||||||
| chr14:70027248
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0001g0213others(10): Show | 15 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1292-2994C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027248 | ||||||
| chr14:70027249
|
G | A | 1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1292-2993G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027249 | ||||||
| chr14:70027275
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1292-2967G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027275 | ||||||
| chr14:70027423
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1292-2819G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027423 | ||||||
| chr14:70027481
|
T | C | 26 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0044others(23): Show | 26 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1292-2761T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027481 | ||||||
| chr14:70027516
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0061others(14): Show | 17 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1292-2726A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027516 | ||||||
| chr14:70027559
|
GT | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-2682delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027559 | ||||||
| chr14:70027657
|
C | T | 1 | a0001c0003t0001g0167 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1292-2585C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027657 | ||||||
| chr14:70027821
|
G | A | 6 | a0001c0001t0007g0032a0001c0001t0007g0034a0001c0001t0007g0095others(3): Show | 6 | HG02055.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-2421G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027821 | ||||||
| chr14:70027947
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0020g0096 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1292-2295C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027947 | ||||||
| chr14:70027953
|
C | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1292-2289C>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70027953 | ||||||
| chr14:70028290
|
G | A | 49 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0135others(46): Show | 50 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1292-1952G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028290 | ||||||
| chr14:70028654
|
A | G | 57 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0135others(54): Show | 58 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1292-1588A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028654 | ||||||
| chr14:70028736
|
C | G | 77 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0060others(74): Show | 78 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1292-1506C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028736 | ||||||
| chr14:70028748
|
G | T | 1 | a0001c0001t0026g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1292-1494G>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028748 | ||||||
| chr14:70028822
|
C | T | 1 | a0001c0001t0022g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1292-1420C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028822 | ||||||
| chr14:70028836
|
C | T | 3 | a0001c0001t0003g0238a0001c0001t0003g0241a0001c0001t0003g0259 | 3 | NA18988.hp1 NA18992.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1292-1406C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028836 | ||||||
| chr14:70028930
|
G | A | 1 | a0001c0001t0020g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-1312G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028930 | ||||||
| chr14:70028992
|
T | C | 1 | a0001c0001t0011g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1292-1250T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70028992 | ||||||
| chr14:70029061
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1292-1181C>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029061 | ||||||
| chr14:70029122
|
T | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(30): Show | 33 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1292-1120T>C | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029122 | ||||||
| chr14:70029136
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1292-1106C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029136 | ||||||
| chr14:70029363
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1292-879G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029363 | ||||||
| chr14:70029406
|
T | A | 1 | a0001c0001t0027g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1292-836T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029406 | ||||||
| chr14:70029508
|
A | G | 3 | a0001c0001t0008g0002a0001c0001t0008g0057a0001c0001t0008g0062 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-734A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029508 | ||||||
| chr14:70029602
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0152a0001c0001t0001g0154others(1): Show | 4 | HG01175.hp2 HG01433.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-640A>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029602 | ||||||
| chr14:70029616
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1292-626G>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029616 | ||||||
| chr14:70029980
|
T | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0188others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-262T>A | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70029980 | ||||||
| chr14:70030150
|
C | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1292-92C>T | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70030150 | ||||||
| chr14:70030202
|
C | CT | 55 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1292-23dupT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70030202 | |||||
| chr14:70030202
|
C | CTT | 7 | a0001c0001t0001g0188a0001c0001t0001g0192a0001c0001t0001g0199others(4): Show | 7 | HG00140.hp1 HG00423.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-24_1292-23dup others(2): Show |
SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70030202 | |||||
| chr14:70030202
|
CT | C | 79 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0079others(76): Show | 80 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1292-23delT | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 70030202 | |||||
| chr14:70030219
|
T | G | 1 | a0001c0001t0011g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1292-23T>G | SMOC1 | ENSG00000198732.11 | transcript | ENST00000361956.8 | protein_coding | 11/11 | chr14 | 70030219 |