Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7871 |
|---|---|
| ensemblid | ENSG00000163681.17 |
| hgncid | 16643 |
| symbol | SLMAP |
| name | sarcolemma associated protein |
| refseq_nuc | NM_001377540.1 |
| refseq_prot | NP_001364469.1 |
| ensembl_nuc | ENST00000671191.1 |
| ensembl_prot | ENSP00000499458.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 57756309 |
| end | 57930003 |
| strand | + |
| ver | v1.2 |
| region | chr3:57756309-57930003 |
| region5000 | chr3:57751309-57935003 |
| regionname0 | SLMAP_chr3_57756309_57930003 |
| regionname5000 | SLMAP_chr3_57751309_57935003 |
| 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 | 842 | 306 | 76 | 59 | 125 | 10 | 34 | 99 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0002 | 0/0 | 842 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0003 | 0/0 | 842 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0004 | 0/0 | 842 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| 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 | 2529 | 200 | 66 | 40 | 62 | 5 | 25 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0002 | 0/0 | 2529 | 95 | 8 | 17 | 57 | 4 | 9 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0003 | 0/0 | 2529 | 4 | 0 | 0 | 4 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0004 | 0/0 | 2529 | 2 | 1 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0005 | 0/0 | 2529 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0006 | 0/0 | 2529 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0007 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0008 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0009 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0010 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| c0011 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3853 | 95 | 21 | 19 | 43 | 4 | 8 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0002 | 0/0 | 3853 | 67 | 2 | 8 | 48 | 2 | 7 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0003 | 1/0 | 3853 | 35 | 23 | 8 | 0 | 1 | 2 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0004 | 0/0 | 3853 | 22 | 2 | 4 | 9 | 0 | 7 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0005 | 0/1 | 3853 | 21 | 0 | 15 | 1 | 1 | 3 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0006 | 0/0 | 3854 | 7 | 4 | 0 | 1 | 0 | 2 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0007 | 0/0 | 3853 | 5 | 0 | 0 | 5 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0008 | 0/0 | 3853 | 5 | 0 | 0 | 5 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0009 | 0/0 | 3853 | 4 | 3 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0010 | 0/0 | 3853 | 4 | 4 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0011 | 0/0 | 3853 | 4 | 3 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0012 | 0/0 | 3854 | 4 | 4 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0013 | 0/0 | 3853 | 4 | 0 | 0 | 4 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0014 | 0/0 | 3853 | 3 | 1 | 1 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0015 | 0/0 | 3853 | 3 | 2 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0016 | 0/0 | 3853 | 3 | 2 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0017 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0018 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0019 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0020 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0021 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0022 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0023 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0024 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0025 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0026 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0027 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0028 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0029 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0030 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0031 | 0/0 | 3854 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0032 | 0/0 | 3854 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0033 | 0/0 | 3854 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0034 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0035 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0036 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0037 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| t0038 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| 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 | 2529 | 200 | 66 | 40 | 62 | 5 | 25 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002 | 0/0 | 2529 | 95 | 8 | 17 | 57 | 4 | 9 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0003 | 0/0 | 2529 | 4 | 0 | 0 | 4 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0004 | 0/0 | 2529 | 2 | 1 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0006 | 0/0 | 2529 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0008 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0009 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0011 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0002c0005 | 0/0 | 2529 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0003c0007 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0004c0010 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6381 | 14 | 13 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0002 | 0/0 | 6381 | 57 | 1 | 8 | 40 | 1 | 7 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0003 | 1/0 | 6381 | 35 | 23 | 8 | 0 | 1 | 2 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0004 | 0/0 | 6381 | 22 | 2 | 4 | 9 | 0 | 7 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0005 | 0/1 | 6381 | 20 | 0 | 14 | 1 | 1 | 3 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0006 | 0/0 | 6382 | 7 | 4 | 0 | 1 | 0 | 2 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0007 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0009 | 0/0 | 6381 | 4 | 3 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0010 | 0/0 | 6381 | 4 | 4 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0011 | 0/0 | 6381 | 4 | 3 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0012 | 0/0 | 6382 | 4 | 4 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0013 | 0/0 | 6381 | 4 | 0 | 0 | 4 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0014 | 0/0 | 6381 | 3 | 1 | 1 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0015 | 0/0 | 6381 | 3 | 2 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0016 | 0/0 | 6381 | 3 | 2 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0018 | 0/0 | 6381 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0020 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0022 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0023 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0025 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0026 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0027 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0032 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0033 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0034 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0035 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0036 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0037 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0001t0038 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0001 | 0/0 | 6381 | 77 | 8 | 17 | 40 | 4 | 8 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0002 | 0/0 | 6381 | 6 | 0 | 0 | 6 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0008 | 0/0 | 6381 | 5 | 0 | 0 | 5 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0017 | 0/0 | 6381 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0019 | 0/0 | 6381 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0021 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0024 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0029 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0002t0030 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0003t0007 | 0/0 | 6381 | 4 | 0 | 0 | 4 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0004t0002 | 0/0 | 6381 | 2 | 1 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0006t0002 | 0/0 | 6381 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0008t0005 | 0/0 | 6381 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0009t0031 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0001c0011t0028 | 0/0 | 6381 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0002c0005t0001 | 0/0 | 6381 | 2 | 0 | 0 | 2 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0003c0007t0001 | 0/0 | 6381 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| a0004c0010t0001 | 0/0 | 6381 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | copy fasta | chr3 | 57751309 | 57935003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0014g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0015g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0016g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0016g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0016g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0018g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0020g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0022g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0023g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0025g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0026g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0032g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0033g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0034g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0035g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0036g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0037g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0001t0038g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0017g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0017g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0019g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0021g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0024g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0029g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0002t0030g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0003t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0003t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0003t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0003t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0004t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0006t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0006t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0008t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0009t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0001c0011t0028g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0002c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0002c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0003c0007t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| a0004c0010t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0023 | g0158 | EUR | GBR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0204 | EUR | GBR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0263 | EUR | FIN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0127 | EUR | FIN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00408 | hp2 | a0001 | c0001 | t0037 | g0071 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00438 | hp2 | a0001 | c0002 | t0008 | g0277 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00609 | hp2 | a0001 | c0002 | t0008 | g0240 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00639 | hp1 | a0001 | c0008 | t0005 | g0172 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | CHS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0181 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01168 | hp1 | a0004 | c0010 | t0001 | g0285 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01175 | hp2 | a0001 | c0011 | t0028 | g0133 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01255 | hp2 | a0001 | c0001 | t0015 | g0139 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01257 | hp2 | a0001 | c0001 | t0014 | g0082 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0162 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0309 | EUR | IBS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0177 | EUR | IBS | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0174 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01934 | hp1 | a0001 | c0001 | t0016 | g0005 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02055 | hp1 | a0001 | c0001 | t0032 | g0004 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02055 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02132 | hp2 | a0001 | c0002 | t0024 | g0216 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02145 | hp1 | a0001 | c0001 | t0026 | g0190 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0102 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0109 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0298 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0179 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02523 | hp1 | a0001 | c0002 | t0008 | g0267 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0112 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0184 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0006 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0300 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02735 | hp1 | a0001 | c0002 | t0019 | g0220 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0301 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0302 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0007 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0303 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02970 | hp1 | a0001 | c0009 | t0031 | g0001 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0175 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0117 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0194 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0111 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03209 | hp1 | a0001 | c0001 | t0033 | g0305 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03492 | hp2 | a0001 | c0001 | t0034 | g0153 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0180 | AFR | GWD | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0191 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03688 | hp2 | a0001 | c0001 | t0020 | g0099 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03831 | hp2 | a0001 | c0001 | t0022 | g0134 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0261 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0114 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0098 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0115 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | STU | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | YRI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18939 | hp2 | a0001 | c0002 | t0030 | g0279 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18941 | hp1 | a0001 | c0001 | t0018 | g0060 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18941 | hp2 | a0001 | c0002 | t0008 | g0223 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18943 | hp1 | a0001 | c0002 | t0017 | g0101 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18943 | hp2 | a0001 | c0001 | t0036 | g0200 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18948 | hp1 | a0001 | c0001 | t0038 | g0047 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18948 | hp2 | a0001 | c0003 | t0007 | g0156 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18949 | hp1 | a0003 | c0007 | t0001 | g0282 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18949 | hp2 | a0001 | c0006 | t0002 | g0012 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18951 | hp2 | a0001 | c0003 | t0007 | g0155 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18957 | hp1 | a0001 | c0003 | t0007 | g0146 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18962 | hp2 | a0001 | c0003 | t0007 | g0151 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18979 | hp1 | a0001 | c0002 | t0029 | g0280 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18980 | hp2 | a0001 | c0001 | t0013 | g0097 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18982 | hp1 | a0001 | c0001 | t0013 | g0079 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18984 | hp1 | a0001 | c0002 | t0008 | g0243 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18989 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18993 | hp2 | a0002 | c0005 | t0001 | g0265 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19002 | hp2 | a0002 | c0005 | t0001 | g0213 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19005 | hp2 | a0001 | c0001 | t0013 | g0078 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19012 | hp1 | a0001 | c0002 | t0021 | g0239 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0003 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19054 | hp2 | a0001 | c0006 | t0002 | g0064 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19066 | hp2 | a0001 | c0001 | t0013 | g0077 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19078 | hp1 | a0001 | c0001 | t0027 | g0246 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19078 | hp2 | a0001 | c0002 | t0017 | g0299 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | YRI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20752 | hp1 | a0001 | c0001 | t0035 | g0132 | EUR | TSI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0262 | EUR | TSI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0207 | EUR | TSI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20805 | hp2 | a0001 | c0004 | t0002 | g0018 | EUR | TSI | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | USA | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | USA | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | USA | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | USA | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0137 | REF | REF | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0143 | REF | REF | SLMAP_chr3_57751309_57935003 | SLMAP | chr3 | 57751309 | 57935003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57849755
|
T | G | 1 | a0003 | 1 | NA18949.hp1 | missense_variant&splice_region_variant | MODERATE | c.458T>G | p.Val153Gly | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/25 | 1596/6381 | 458/2529 | 153/842 | chr3 | 57849755 | ||
| chr3:57861982
|
C | T | 1 | a0002 | 2 | NA18993.hp2 NA19002.hp2 |
missense_variant | MODERATE | c.862C>T | p.His288Tyr | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/25 | 2000/6381 | 862/2529 | 288/842 | chr3 | 57861982 | ||
| chr3:57913179
|
A | G | 1 | a0004 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.2042A>G | p.Lys681Arg | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/25 | 3180/6381 | 2042/2529 | 681/842 | chr3 | 57913179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57757744
|
C | T | 1 | a0001c0006 | 2 | NA18949.hp2 NA19054.hp2 |
synonymous_variant | LOW | c.93C>T | p.Gly31Gly | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 1231/6381 | 93/2529 | 31/842 | chr3 | 57757744 | ||
| chr3:57831481
|
C | T | 1 | a0001c0011 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.297C>T | p.Ser99Ser | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/25 | 1435/6381 | 297/2529 | 99/842 | chr3 | 57831481 | ||
| chr3:57858123
|
A | G | 1 | a0001c0003 | 4 | NA18948.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
synonymous_variant | LOW | c.651A>G | p.Leu217Leu | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/25 | 1789/6381 | 651/2529 | 217/842 | chr3 | 57858123 | ||
| chr3:57896874
|
C | T | 4 | a0001c0002a0002c0005a0003c0007others(1): Show | 99 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
splice_region_variant&synonymous_variant | LOW | c.1443C>T | p.Asp481Asp | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/25 | 2581/6381 | 1443/2529 | 481/842 | chr3 | 57896874 | ||
| chr3:57912649
|
T | A | 1 | a0001c0004 | 2 | HG02055.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.1968T>A | p.Leu656Leu | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 20/25 | 3106/6381 | 1968/2529 | 656/842 | chr3 | 57912649 | ||
| chr3:57913201
|
C | T | 1 | a0001c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2064C>T | p.Thr688Thr | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/25 | 3202/6381 | 2064/2529 | 688/842 | chr3 | 57913201 | ||
| chr3:57916912
|
G | A | 1 | a0001c0008 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.2145G>A | p.Gln715Gln | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/25 | 3283/6381 | 2145/2529 | 715/842 | chr3 | 57916912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57756610
|
G | C | 1 | a0001c0001t0014 | 3 | HG01257.hp2 HG02145.hp2 HG04184.hp1 |
5_prime_UTR_variant | MODIFIER | c.-1042G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 1042 | chr3 | 57756610 | |||||
| chr3:57756709
|
C | G | 1 | a0001c0001t0016 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-943C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 943 | chr3 | 57756709 | |||||
| chr3:57756773
|
G | A | 1 | a0001c0002t0019 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-879G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 879 | chr3 | 57756773 | |||||
| chr3:57756774
|
G | A | 1 | a0001c0001t0020 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-878G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 878 | chr3 | 57756774 | |||||
| chr3:57756792
|
C | A | 1 | a0001c0002t0021 | 1 | NA19012.hp1 | 5_prime_UTR_variant | MODIFIER | c.-860C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 860 | chr3 | 57756792 | |||||
| chr3:57756946
|
C | T | 1 | a0001c0001t0038 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-706C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 706 | chr3 | 57756946 | |||||
| chr3:57756998
|
G | T | 17 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(14): Show | 124 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
5_prime_UTR_variant | MODIFIER | c.-654G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 654 | chr3 | 57756998 | |||||
| chr3:57756999
|
C | T | 1 | a0001c0001t0013 | 4 | NA18980.hp2 NA18982.hp1 NA19005.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-653C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 653 | chr3 | 57756999 | |||||
| chr3:57757230
|
A | G | 1 | a0001c0001t0035 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-422A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 422 | chr3 | 57757230 | |||||
| chr3:57757278
|
A | G | 1 | a0001c0001t0034 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-374A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 374 | chr3 | 57757278 | |||||
| chr3:57757431
|
C | A | 1 | a0001c0001t0022 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-221C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 221 | chr3 | 57757431 | |||||
| chr3:57757519
|
G | A | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0022others(4): Show | 29 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-133G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 133 | chr3 | 57757519 | |||||
| chr3:57757609
|
C | T | 1 | a0001c0001t0037 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 43 | chr3 | 57757609 | |||||
| chr3:57757610
|
C | G | 9 | a0001c0001t0002a0001c0001t0018a0001c0001t0036others(6): Show | 77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-42C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/25 | 42 | chr3 | 57757610 | |||||
| chr3:57927406
|
G | A | 2 | a0001c0001t0007a0001c0003t0007 | 5 | NA18948.hp2 NA18951.hp2 NA18957.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*117G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 1478 | chr3 | 57927406 | |||||
| chr3:57927669
|
G | A | 1 | a0001c0002t0024 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 1741 | chr3 | 57927669 | |||||
| chr3:57927734
|
G | A | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 1806 | chr3 | 57927734 | |||||
| chr3:57927838
|
A | G | 3 | a0001c0001t0010a0001c0001t0016a0001c0001t0033 | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 1910 | chr3 | 57927838 | |||||
| chr3:57927929
|
A | C | 1 | a0001c0001t0015 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*640A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2001 | chr3 | 57927929 | |||||
| chr3:57927942
|
A | AT | 4 | a0001c0001t0012a0001c0001t0032a0001c0001t0033others(1): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*666dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2028 | INFO_REALIGN_3_PRIME | chr3 | 57927942 | ||||
| chr3:57927987
|
A | G | 13 | a0001c0001t0001a0001c0001t0009a0001c0002t0001others(10): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*698A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2059 | chr3 | 57927987 | |||||
| chr3:57928008
|
T | C | 1 | a0001c0001t0016 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2080 | chr3 | 57928008 | |||||
| chr3:57928083
|
G | A | 2 | a0001c0001t0023a0001c0009t0031 | 2 | HG00099.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2155 | chr3 | 57928083 | |||||
| chr3:57928264
|
A | AT | 1 | a0001c0001t0006 | 7 | HG00544.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*985dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2347 | INFO_REALIGN_3_PRIME | chr3 | 57928264 | ||||
| chr3:57928423
|
G | A | 1 | a0001c0009t0031 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1134G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2495 | chr3 | 57928423 | |||||
| chr3:57928451
|
T | C | 15 | a0001c0001t0001a0001c0001t0009a0001c0001t0026others(12): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1162T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2523 | chr3 | 57928451 | |||||
| chr3:57928591
|
C | T | 1 | a0001c0001t0033 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2663 | chr3 | 57928591 | |||||
| chr3:57928868
|
G | A | 2 | a0001c0001t0025a0001c0001t0032 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1579G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 2940 | chr3 | 57928868 | |||||
| chr3:57928956
|
T | C | 1 | a0001c0001t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3028 | chr3 | 57928956 | |||||
| chr3:57929128
|
C | T | 1 | a0001c0009t0031 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1839C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3200 | chr3 | 57929128 | |||||
| chr3:57929321
|
G | A | 1 | a0001c0002t0029 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3393 | chr3 | 57929321 | |||||
| chr3:57929372
|
A | G | 1 | a0001c0001t0018 | 2 | NA18941.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2083A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3444 | chr3 | 57929372 | |||||
| chr3:57929480
|
C | G | 1 | a0001c0002t0030 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2191C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3552 | chr3 | 57929480 | |||||
| chr3:57929627
|
A | C | 1 | a0001c0001t0012 | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2338A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3699 | chr3 | 57929627 | |||||
| chr3:57929635
|
A | G | 1 | a0001c0001t0012 | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2346A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3707 | chr3 | 57929635 | |||||
| chr3:57929702
|
C | T | 1 | a0001c0001t0009 | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2413C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3774 | chr3 | 57929702 | |||||
| chr3:57929708
|
G | T | 1 | a0001c0011t0028 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2419G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3780 | chr3 | 57929708 | |||||
| chr3:57929747
|
A | C | 7 | a0001c0001t0004a0001c0001t0012a0001c0001t0013others(4): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2458A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3819 | chr3 | 57929747 | |||||
| chr3:57929836
|
T | C | 1 | a0001c0001t0011 | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2547T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 3908 | chr3 | 57929836 | |||||
| chr3:57929940
|
A | G | 2 | a0001c0001t0025a0001c0001t0032 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2651A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 25/25 | 4012 | chr3 | 57929940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57756518
|
G | T | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-1104-30G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 1/24 | chr3 | 57756518 | ||||||
| chr3:57756545
|
C | T | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02622.hp2 HG02717.hp2 |
splice_region_variant&intron_variant | LOW | c.-1104-3C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 1/24 | chr3 | 57756545 | ||||||
| chr3:57757967
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+118G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57757967 | ||||||
| chr3:57758371
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.198+522C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57758371 | ||||||
| chr3:57758515
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+666G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57758515 | ||||||
| chr3:57758875
|
T | C | 1 | a0001c0001t0018g0002 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.198+1026T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57758875 | ||||||
| chr3:57758898
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+1049A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57758898 | ||||||
| chr3:57758921
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198+1072C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57758921 | ||||||
| chr3:57759032
|
G | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1183G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759032 | ||||||
| chr3:57759139
|
C | T | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.198+1290C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759139 | ||||||
| chr3:57759273
|
G | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+1424G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759273 | ||||||
| chr3:57759279
|
C | CT | 13 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(10): Show | 13 | HG02258.hp2 HG02293.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+1445dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57759279 | |||||
| chr3:57759311
|
C | T | 93 | a0001c0001t0027g0246a0001c0001t0036g0200a0001c0002t0001g0196others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.198+1462C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759311 | ||||||
| chr3:57759399
|
T | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+1550T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759399 | ||||||
| chr3:57759426
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+1577C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759426 | ||||||
| chr3:57759574
|
C | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+1725C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759574 | ||||||
| chr3:57759810
|
C | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+1961C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759810 | ||||||
| chr3:57759905
|
G | A | 127 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(124): Show | 127 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.198+2056G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57759905 | ||||||
| chr3:57760078
|
C | G | 1 | a0001c0001t0005g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.198+2229C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760078 | ||||||
| chr3:57760104
|
T | C | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+2255T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760104 | ||||||
| chr3:57760343
|
A | T | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.198+2494A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760343 | ||||||
| chr3:57760712
|
C | G | 1 | a0001c0001t0003g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198+2863C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760712 | ||||||
| chr3:57760747
|
G | C | 236 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(233): Show | 236 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.198+2898G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760747 | ||||||
| chr3:57760788
|
C | T | 109 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.198+2939C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760788 | ||||||
| chr3:57760950
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+3101C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57760950 | ||||||
| chr3:57761072
|
A | G | 45 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(42): Show | 45 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.198+3223A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761072 | ||||||
| chr3:57761240
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+3391G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761240 | ||||||
| chr3:57761318
|
G | A | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198+3469G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761318 | ||||||
| chr3:57761446
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+3597C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761446 | ||||||
| chr3:57761458
|
C | G | 3 | a0001c0001t0006g0113a0001c0001t0006g0114a0001c0001t0006g0115 | 3 | HG00544.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.198+3609C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761458 | ||||||
| chr3:57761483
|
C | G | 3 | a0001c0001t0006g0113a0001c0001t0006g0114a0001c0001t0006g0115 | 3 | HG00544.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.198+3634C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761483 | ||||||
| chr3:57761527
|
T | C | 11 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+3678T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761527 | ||||||
| chr3:57761662
|
C | A | 165 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(162): Show | 165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.198+3813C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761662 | ||||||
| chr3:57761666
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+3817C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761666 | ||||||
| chr3:57761769
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0033g0305 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+3920C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761769 | ||||||
| chr3:57761815
|
A | G | 3 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0037g0071 | 3 | HG00408.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.198+3966A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761815 | ||||||
| chr3:57761910
|
G | A | 42 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(39): Show | 42 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.198+4061G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57761910 | ||||||
| chr3:57762053
|
C | CA | 16 | a0001c0001t0001g0287a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 16 | HG00408.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+4225dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57762053 | |||||
| chr3:57762053
|
CA | C | 7 | a0001c0001t0002g0069a0001c0001t0005g0194a0001c0001t0016g0005others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+4225delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57762053 | |||||
| chr3:57762127
|
G | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+4278G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762127 | ||||||
| chr3:57762308
|
G | A | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+4459G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762308 | ||||||
| chr3:57762337
|
C | A | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.198+4488C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762337 | ||||||
| chr3:57762710
|
G | GT | 93 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(90): Show | 93 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.198+4884dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57762710 | |||||
| chr3:57762710
|
G | GTT | 20 | a0001c0001t0004g0104a0001c0001t0004g0105a0001c0001t0004g0106others(17): Show | 20 | HG01175.hp2 HG01361.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.198+4883_198+4884d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57762710 | |||||
| chr3:57762715
|
T | G | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+4866T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762715 | ||||||
| chr3:57762976
|
G | A | 39 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(36): Show | 39 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.198+5127G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762976 | ||||||
| chr3:57762998
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.198+5149A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57762998 | ||||||
| chr3:57763047
|
T | C | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.198+5198T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763047 | ||||||
| chr3:57763063
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+5214C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763063 | ||||||
| chr3:57763069
|
A | G | 44 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(41): Show | 44 | HG00544.hp2 HG01099.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.198+5220A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763069 | ||||||
| chr3:57763129
|
G | C | 1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+5280G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763129 | ||||||
| chr3:57763172
|
G | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG03017.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.198+5323G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763172 | ||||||
| chr3:57763277
|
C | CT | 11 | a0001c0001t0002g0052a0001c0001t0002g0067a0001c0001t0002g0068others(8): Show | 11 | HG01169.hp1 HG01934.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+5443dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57763277 | |||||
| chr3:57763277
|
CT | C | 6 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192others(3): Show | 6 | HG00544.hp2 HG01891.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+5443delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57763277 | |||||
| chr3:57763307
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+5458C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763307 | ||||||
| chr3:57763422
|
A | G | 10 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249others(7): Show | 10 | HG00673.hp2 HG02040.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+5573A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763422 | ||||||
| chr3:57763459
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.198+5610G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763459 | ||||||
| chr3:57763721
|
A | T | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+5872A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763721 | ||||||
| chr3:57763834
|
A | G | 131 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(128): Show | 131 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.198+5985A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763834 | ||||||
| chr3:57763940
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198+6091G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57763940 | ||||||
| chr3:57764226
|
G | T | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.198+6377G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764226 | ||||||
| chr3:57764361
|
G | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+6512G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764361 | ||||||
| chr3:57764377
|
C | G | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.198+6528C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764377 | ||||||
| chr3:57764473
|
A | G | 165 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(162): Show | 165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.198+6624A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764473 | ||||||
| chr3:57764501
|
C | CA | 75 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(72): Show | 75 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.198+6663dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57764501 | |||||
| chr3:57764512
|
AG | A | 5 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(2): Show | 5 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+6664delG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764512 | ||||||
| chr3:57764513
|
G | A | 237 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(234): Show | 237 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.198+6664G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764513 | ||||||
| chr3:57764518
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+6669G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764518 | ||||||
| chr3:57764522
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+6673A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764522 | ||||||
| chr3:57764523
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+6674G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764523 | ||||||
| chr3:57764868
|
G | A | 12 | a0001c0002t0001g0197a0001c0002t0001g0203a0001c0002t0001g0204others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+7019G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764868 | ||||||
| chr3:57764959
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+7110G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57764959 | ||||||
| chr3:57765054
|
TAA | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+7209_198+7210d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57765054 | |||||
| chr3:57765263
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.198+7414G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765263 | ||||||
| chr3:57765305
|
A | G | 240 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(237): Show | 240 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.198+7456A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765305 | ||||||
| chr3:57765374
|
T | C | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+7525T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765374 | ||||||
| chr3:57765418
|
T | G | 1 | a0001c0002t0001g0264 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.198+7569T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765418 | ||||||
| chr3:57765493
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0066 | 2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.198+7644A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765493 | ||||||
| chr3:57765633
|
T | A | 1 | a0001c0001t0006g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.198+7784T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765633 | ||||||
| chr3:57765923
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+8074T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765923 | ||||||
| chr3:57765928
|
C | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+8079C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57765928 | ||||||
| chr3:57766000
|
C | CT | 14 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0002g0195others(11): Show | 14 | HG01106.hp2 HG01891.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+8167dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766000 | |||||
| chr3:57766085
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+8236G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766085 | ||||||
| chr3:57766131
|
T | C | 114 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.198+8282T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766131 | ||||||
| chr3:57766159
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198+8310C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766159 | ||||||
| chr3:57766165
|
A | AT | 17 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(14): Show | 17 | HG00609.hp1 HG01106.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+8340dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766165
|
A | ATT | 6 | a0001c0001t0002g0286a0001c0001t0010g0301a0001c0001t0010g0302others(3): Show | 6 | HG01934.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+8339_198+8340d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766165
|
A | ATTTTT | 79 | a0001c0001t0001g0119a0001c0001t0001g0287a0001c0001t0001g0288others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.198+8336_198+8340d others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766165
|
A | ATTTTTT | 30 | a0001c0001t0001g0122a0001c0001t0001g0295a0001c0001t0027g0246others(27): Show | 30 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.198+8335_198+8340d others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766165
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+8331_198+8340d others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766165
|
AT | A | 32 | a0001c0001t0002g0014a0001c0001t0003g0124a0001c0001t0004g0075others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.198+8340delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766165 | |||||
| chr3:57766250
|
T | C | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198+8401T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766250 | ||||||
| chr3:57766258
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+8409C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766258 | ||||||
| chr3:57766396
|
T | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+8547T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766396 | ||||||
| chr3:57766545
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.198+8696A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766545 | ||||||
| chr3:57766572
|
T | G | 1 | a0001c0001t0016g0005 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.198+8723T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766572 | ||||||
| chr3:57766637
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+8788A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766637 | ||||||
| chr3:57766667
|
C | G | 1 | a0001c0002t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.198+8818C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766667 | ||||||
| chr3:57766896
|
CTTTA | C | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+9051_198+9054d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57766896 | |||||
| chr3:57766903
|
TC | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+9055delC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766903 | ||||||
| chr3:57766913
|
A | T | 1 | a0001c0002t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+9064A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766913 | ||||||
| chr3:57766977
|
G | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+9128G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57766977 | ||||||
| chr3:57767033
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198+9184C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767033 | ||||||
| chr3:57767162
|
A | C | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.198+9313A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767162 | ||||||
| chr3:57767275
|
T | C | 1 | a0001c0001t0005g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198+9426T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767275 | ||||||
| chr3:57767538
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.198+9689T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767538 | ||||||
| chr3:57767582
|
T | G | 1 | a0001c0001t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198+9733T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767582 | ||||||
| chr3:57767692
|
G | C | 240 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(237): Show | 240 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.198+9843G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767692 | ||||||
| chr3:57767780
|
G | A | 79 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.198+9931G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767780 | ||||||
| chr3:57767858
|
C | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.198+10009C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57767858 | ||||||
| chr3:57768071
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+10222A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768071 | ||||||
| chr3:57768187
|
G | A | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+10338G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768187 | ||||||
| chr3:57768264
|
A | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+10415A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768264 | ||||||
| chr3:57768354
|
G | C | 1 | a0001c0001t0001g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.198+10505G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768354 | ||||||
| chr3:57768672
|
C | G | 1 | a0001c0002t0001g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.198+10823C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768672 | ||||||
| chr3:57768763
|
T | G | 6 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0051others(3): Show | 6 | NA18974.hp2 NA18984.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+10914T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768763 | ||||||
| chr3:57768802
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+10953C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768802 | ||||||
| chr3:57768993
|
A | G | 1 | a0001c0001t0006g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.198+11144A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57768993 | ||||||
| chr3:57769032
|
C | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.198+11183C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769032 | ||||||
| chr3:57769068
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.198+11219G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769068 | ||||||
| chr3:57769095
|
T | C | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+11246T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769095 | ||||||
| chr3:57769266
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+11417C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769266 | ||||||
| chr3:57769293
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.198+11444C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769293 | ||||||
| chr3:57769439
|
C | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+11590C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769439 | ||||||
| chr3:57769511
|
C | T | 6 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+11662C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769511 | ||||||
| chr3:57769525
|
A | G | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.198+11676A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769525 | ||||||
| chr3:57769579
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198+11730C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769579 | ||||||
| chr3:57769928
|
G | T | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.198+12079G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769928 | ||||||
| chr3:57769972
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+12123T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57769972 | ||||||
| chr3:57770127
|
A | C | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.198+12278A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57770127 | ||||||
| chr3:57770169
|
G | A | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+12320G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57770169 | ||||||
| chr3:57770633
|
G | A | 1 | a0001c0002t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198+12784G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57770633 | ||||||
| chr3:57770775
|
G | C | 1 | a0001c0001t0002g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198+12926G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57770775 | ||||||
| chr3:57770938
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.198+13089T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57770938 | ||||||
| chr3:57771100
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+13251C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771100 | ||||||
| chr3:57771143
|
T | TCTCCC | 3 | a0001c0001t0003g0138a0001c0001t0003g0307a0001c0001t0003g0308 | 3 | HG02622.hp2 HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.198+13328_198+1333 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771143 | |||||
| chr3:57771143
|
TCTCCC | T | 226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.198+13328_198+1333 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771143 | |||||
| chr3:57771143
|
TCTCCCCT others(3): Show |
T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+13323_198+1333 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771143 | |||||
| chr3:57771143
|
TCTCCCCT others(8): Show |
T | 3 | a0001c0001t0002g0039a0001c0001t0002g0065a0001c0001t0002g0069 | 3 | HG00438.hp1 HG02056.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.198+13318_198+1333 others(19): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771143 | |||||
| chr3:57771143
|
TCTCCCCT others(13): Show |
T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+13313_198+1333 others(24): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771143 | |||||
| chr3:57771164
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.198+13315C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771164 | ||||||
| chr3:57771177
|
C | CCCTCT | 251 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.198+13338_198+1334 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771177 | |||||
| chr3:57771177
|
C | CCCTCTCC others(3): Show |
1 | a0001c0001t0002g0038 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.198+13333_198+1334 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771177 | |||||
| chr3:57771177
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.198+13328C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771177 | ||||||
| chr3:57771192
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+13343C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771192 | ||||||
| chr3:57771194
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+13345T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771194 | ||||||
| chr3:57771199
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+13350T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771199 | ||||||
| chr3:57771205
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+13356C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771205 | ||||||
| chr3:57771207
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+13358C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771207 | ||||||
| chr3:57771220
|
T | TGA | 49 | a0001c0001t0001g0291a0001c0001t0004g0075a0001c0001t0004g0076others(46): Show | 49 | HG00544.hp2 HG01109.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.198+13393_198+1339 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771220 | |||||
| chr3:57771220
|
TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+13385_198+1339 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57771220 | |||||
| chr3:57771244
|
G | A | 1 | a0001c0001t0004g0080 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.198+13395G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771244 | ||||||
| chr3:57771281
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.198+13432A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771281 | ||||||
| chr3:57771362
|
A | G | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198+13513A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771362 | ||||||
| chr3:57771464
|
C | G | 1 | a0001c0001t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198+13615C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771464 | ||||||
| chr3:57771570
|
C | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG03017.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.198+13721C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771570 | ||||||
| chr3:57771608
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+13759C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771608 | ||||||
| chr3:57771855
|
G | C | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+14006G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771855 | ||||||
| chr3:57771907
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.198+14058C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57771907 | ||||||
| chr3:57772119
|
A | C | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062 | 3 | NA18980.hp1 NA18999.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.198+14270A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772119 | ||||||
| chr3:57772182
|
A | C | 3 | a0001c0001t0006g0113a0001c0001t0006g0114a0001c0001t0006g0115 | 3 | HG00544.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.198+14333A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772182 | ||||||
| chr3:57772341
|
T | G | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.198+14492T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772341 | ||||||
| chr3:57772432
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.198+14583G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772432 | ||||||
| chr3:57772645
|
A | AT | 8 | a0001c0001t0001g0136a0001c0001t0003g0123a0001c0001t0003g0182others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+14808dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57772645 | |||||
| chr3:57772723
|
C | T | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198+14874C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772723 | ||||||
| chr3:57772928
|
T | C | 240 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(237): Show | 240 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.198+15079T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57772928 | ||||||
| chr3:57773102
|
C | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062 | 3 | NA18980.hp1 NA18999.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.198+15253C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57773102 | ||||||
| chr3:57773623
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+15774C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57773623 | ||||||
| chr3:57773830
|
G | A | 4 | a0001c0002t0001g0215a0001c0002t0001g0217a0001c0002t0001g0275others(1): Show | 4 | HG02080.hp2 HG02132.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+15981G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57773830 | ||||||
| chr3:57774489
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+16640G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774489 | ||||||
| chr3:57774509
|
A | AATT | 9 | a0001c0001t0003g0125a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG00735.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+16691_198+1669 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774509
|
A | AATTATTA others(2): Show |
4 | a0001c0001t0003g0167a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02451.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+16685_198+1669 others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774509
|
A | AATTATTA others(5): Show |
1 | a0001c0001t0010g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.198+16682_198+1669 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774509
|
AATT | A | 43 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0288others(40): Show | 43 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.198+16691_198+1669 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774509
|
AATTATT | A | 219 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0001g0287others(216): Show | 219 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.198+16688_198+1669 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774509
|
AATTATTA others(5): Show |
A | 3 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0186 | 3 | HG01243.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.198+16682_198+1669 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57774509 | |||||
| chr3:57774551
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+16702G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774551 | ||||||
| chr3:57774698
|
C | T | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+16849C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774698 | ||||||
| chr3:57774727
|
T | C | 2 | a0001c0002t0001g0218a0001c0002t0021g0239 | 2 | NA18977.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.198+16878T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774727 | ||||||
| chr3:57774814
|
G | A | 3 | a0001c0002t0001g0219a0002c0005t0001g0213a0002c0005t0001g0265 | 3 | NA18968.hp2 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.198+16965G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774814 | ||||||
| chr3:57774876
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+17027C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774876 | ||||||
| chr3:57774972
|
C | T | 1 | a0001c0001t0011g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+17123C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57774972 | ||||||
| chr3:57775060
|
CT | C | 26 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.198+17223delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775060 | |||||
| chr3:57775085
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+17236C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775085 | ||||||
| chr3:57775173
|
G | GC | 239 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(236): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.198+17329dupC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775173 | |||||
| chr3:57775192
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+17343T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775192 | ||||||
| chr3:57775259
|
G | C | 1 | a0001c0002t0019g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.198+17410G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775259 | ||||||
| chr3:57775285
|
G | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+17436G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775285 | ||||||
| chr3:57775322
|
G | T | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+17473G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775322 | ||||||
| chr3:57775444
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+17595A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775444 | ||||||
| chr3:57775507
|
TAC | T | 9 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0292others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+17660_198+1766 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775507 | |||||
| chr3:57775508
|
AC | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0288a0001c0001t0001g0291others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+17660delC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775508 | ||||||
| chr3:57775509
|
C | A | 3 | a0001c0001t0001g0120a0001c0001t0009g0116a0001c0001t0009g0121 | 3 | HG01109.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.198+17660C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775509 | ||||||
| chr3:57775509
|
C | CA | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0019others(121): Show | 124 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.198+17689dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775509 | |||||
| chr3:57775509
|
C | CAA | 21 | a0001c0001t0001g0136a0001c0001t0002g0017a0001c0001t0006g0096others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.198+17688_198+1768 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775509 | |||||
| chr3:57775509
|
CA | C | 8 | a0001c0001t0002g0069a0001c0001t0032g0004a0001c0002t0001g0236others(5): Show | 8 | HG01169.hp1 HG02055.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+17689delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775509 | |||||
| chr3:57775509
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+17679_198+1768 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57775509 | |||||
| chr3:57775806
|
C | A | 1 | a0001c0002t0001g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+17957C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775806 | ||||||
| chr3:57775943
|
G | A | 33 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(30): Show | 33 | HG01109.hp2 HG01243.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+18094G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57775943 | ||||||
| chr3:57776478
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198+18629A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776478 | ||||||
| chr3:57776504
|
C | T | 1 | a0001c0001t0004g0080 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.198+18655C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776504 | ||||||
| chr3:57776506
|
T | TTC | 23 | a0001c0001t0002g0041a0001c0001t0027g0246a0001c0002t0001g0202others(20): Show | 23 | HG00673.hp2 HG01928.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+18673_198+1867 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57776506 | |||||
| chr3:57776506
|
T | TTCTCTC | 51 | a0001c0001t0009g0116a0001c0001t0009g0118a0001c0001t0009g0121others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.198+18669_198+1867 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57776506 | |||||
| chr3:57776519
|
TCTC | T | 4 | a0001c0001t0005g0135a0001c0001t0005g0177a0001c0001t0005g0178others(1): Show | 4 | HG00099.hp1 HG00741.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+18671_198+1867 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776519 | ||||||
| chr3:57776522
|
C | CT | 30 | a0001c0001t0003g0141a0001c0001t0003g0189a0001c0001t0004g0089others(27): Show | 30 | HG00639.hp1 HG00733.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.198+18694dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57776522 | |||||
| chr3:57776522
|
C | CTCTCTCT | 15 | a0001c0002t0001g0197a0001c0002t0001g0207a0001c0002t0001g0208others(12): Show | 15 | HG00621.hp2 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+18674_198+1867 others(11): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57776522 | |||||
| chr3:57776522
|
C | CTCTCTT | 15 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(12): Show | 15 | HG01243.hp1 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+18674_198+1867 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57776522 | |||||
| chr3:57776522
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+18673C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776522 | ||||||
| chr3:57776523
|
T | TCTCTC | 3 | a0001c0001t0009g0117a0001c0002t0001g0219a0001c0002t0001g0269 | 3 | HG02976.hp2 NA18968.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.198+18674_198+1867 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776523 | ||||||
| chr3:57776524
|
T | C | 2 | a0001c0001t0004g0092a0001c0002t0001g0231 | 2 | HG01069.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.198+18675T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776524 | ||||||
| chr3:57776525
|
T | C | 2 | a0001c0001t0020g0099a0001c0002t0001g0235 | 2 | HG01071.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.198+18676T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776525 | ||||||
| chr3:57776609
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+18760C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776609 | ||||||
| chr3:57776700
|
G | A | 1 | a0001c0001t0006g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.198+18851G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776700 | ||||||
| chr3:57776758
|
C | G | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.198+18909C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776758 | ||||||
| chr3:57776937
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.198+19088C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57776937 | ||||||
| chr3:57777093
|
T | C | 1 | a0001c0001t0006g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+19244T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777093 | ||||||
| chr3:57777155
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.198+19306C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777155 | ||||||
| chr3:57777169
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+19320C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777169 | ||||||
| chr3:57777207
|
A | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+19358A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777207 | ||||||
| chr3:57777259
|
A | T | 1 | a0001c0002t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.198+19410A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777259 | ||||||
| chr3:57777286
|
T | A | 30 | a0001c0001t0003g0141a0001c0001t0005g0135a0001c0001t0005g0137others(27): Show | 30 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.198+19437T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777286 | ||||||
| chr3:57777352
|
A | ATAAG | 235 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(232): Show | 235 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.198+19506_198+1950 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57777352 | |||||
| chr3:57777582
|
A | T | 1 | a0001c0001t0011g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.198+19733A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777582 | ||||||
| chr3:57777590
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+19741G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777590 | ||||||
| chr3:57777655
|
A | G | 1 | a0001c0002t0001g0251 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.198+19806A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777655 | ||||||
| chr3:57777827
|
C | T | 6 | a0001c0001t0002g0024a0001c0001t0002g0038a0001c0001t0002g0072others(3): Show | 6 | HG00408.hp2 HG02523.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+19978C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777827 | ||||||
| chr3:57777915
|
G | A | 242 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(239): Show | 242 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.198+20066G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57777915 | ||||||
| chr3:57778028
|
A | G | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.198+20179A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778028 | ||||||
| chr3:57778470
|
A | G | 277 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.198+20621A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778470 | ||||||
| chr3:57778482
|
C | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+20633C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778482 | ||||||
| chr3:57778570
|
C | CT | 12 | a0001c0001t0001g0120a0001c0001t0002g0011a0001c0001t0002g0039others(9): Show | 12 | HG00438.hp1 HG01978.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+20740dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57778570 | |||||
| chr3:57778570
|
CT | C | 6 | a0001c0001t0002g0019a0001c0001t0004g0093a0001c0001t0004g0094others(3): Show | 6 | HG01168.hp1 HG01175.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+20740delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57778570 | |||||
| chr3:57778574
|
T | C | 10 | a0001c0001t0002g0058a0001c0001t0010g0300a0001c0001t0010g0301others(7): Show | 10 | HG00673.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+20725T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778574 | ||||||
| chr3:57778656
|
C | T | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198+20807C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778656 | ||||||
| chr3:57778913
|
T | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+21064T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778913 | ||||||
| chr3:57778988
|
G | A | 34 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(31): Show | 34 | HG01109.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.198+21139G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57778988 | ||||||
| chr3:57779084
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+21235G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779084 | ||||||
| chr3:57779494
|
G | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+21645G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779494 | ||||||
| chr3:57779508
|
C | CA | 12 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0129others(9): Show | 12 | HG01928.hp1 HG01943.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+21676dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57779508 | |||||
| chr3:57779508
|
CA | C | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(73): Show | 76 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.198+21676delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57779508 | |||||
| chr3:57779526
|
C | A | 6 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0154others(3): Show | 6 | HG00609.hp2 HG00733.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+21677C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779526 | ||||||
| chr3:57779693
|
G | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+21844G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779693 | ||||||
| chr3:57779829
|
A | C | 1 | a0001c0001t0004g0085 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.198+21980A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779829 | ||||||
| chr3:57779917
|
T | C | 235 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(232): Show | 235 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.198+22068T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779917 | ||||||
| chr3:57779931
|
A | G | 6 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0228others(3): Show | 6 | NA18944.hp1 NA18962.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+22082A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779931 | ||||||
| chr3:57779966
|
A | T | 1 | a0001c0001t0005g0157 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.198+22117A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57779966 | ||||||
| chr3:57780135
|
T | C | 189 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(186): Show | 189 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.198+22286T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57780135 | ||||||
| chr3:57780272
|
G | A | 9 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+22423G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57780272 | ||||||
| chr3:57780557
|
G | A | 1 | a0001c0008t0005g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.198+22708G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57780557 | ||||||
| chr3:57780721
|
G | A | 1 | a0001c0001t0004g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.198+22872G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57780721 | ||||||
| chr3:57780774
|
G | T | 1 | a0001c0001t0035g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.198+22925G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57780774 | ||||||
| chr3:57781003
|
CAT | C | 79 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.198+23164_198+2316 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57781003 | |||||
| chr3:57781004
|
A | G | 1 | a0001c0002t0001g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.198+23155A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781004 | ||||||
| chr3:57781041
|
C | T | 1 | a0001c0008t0005g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.198+23192C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781041 | ||||||
| chr3:57781043
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+23194C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781043 | ||||||
| chr3:57781184
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.198+23335A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781184 | ||||||
| chr3:57781207
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+23358A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781207 | ||||||
| chr3:57781305
|
T | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+23456T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781305 | ||||||
| chr3:57781467
|
C | T | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.198+23618C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781467 | ||||||
| chr3:57781503
|
A | G | 1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+23654A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781503 | ||||||
| chr3:57781586
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.198+23737G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781586 | ||||||
| chr3:57781729
|
A | AT | 19 | a0001c0001t0001g0136a0001c0001t0003g0008a0001c0001t0003g0129others(16): Show | 19 | HG00733.hp1 HG01099.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+23901dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57781729 | |||||
| chr3:57781729
|
A | ATT | 193 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0287others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.198+23900_198+2390 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57781729 | |||||
| chr3:57781729
|
A | ATTT | 29 | a0001c0001t0001g0120a0001c0001t0002g0034a0001c0001t0002g0035others(26): Show | 29 | HG00735.hp2 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.198+23899_198+2390 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57781729 | |||||
| chr3:57781794
|
G | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+23945G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781794 | ||||||
| chr3:57781894
|
A | G | 79 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(76): Show | 79 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.198+24045A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57781894 | ||||||
| chr3:57782091
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+24242G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782091 | ||||||
| chr3:57782158
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.198+24309G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782158 | ||||||
| chr3:57782346
|
A | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+24497A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782346 | ||||||
| chr3:57782392
|
G | A | 3 | a0001c0001t0002g0043a0001c0001t0002g0053a0001c0001t0002g0054 | 3 | HG03017.hp1 NA18947.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.198+24543G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782392 | ||||||
| chr3:57782424
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+24575A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782424 | ||||||
| chr3:57782427
|
A | G | 1 | a0001c0002t0001g0264 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.198+24578A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782427 | ||||||
| chr3:57782642
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.198+24793T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782642 | ||||||
| chr3:57782758
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+24909C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782758 | ||||||
| chr3:57782889
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.198+25040C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782889 | ||||||
| chr3:57782905
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.198+25056A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782905 | ||||||
| chr3:57782940
|
C | T | 1 | a0001c0001t0005g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.198+25091C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57782940 | ||||||
| chr3:57783062
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198+25213A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783062 | ||||||
| chr3:57783110
|
C | T | 5 | a0001c0002t0001g0196a0001c0002t0001g0199a0001c0002t0001g0237others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+25261C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783110 | ||||||
| chr3:57783146
|
G | A | 1 | a0001c0001t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.198+25297G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783146 | ||||||
| chr3:57783458
|
T | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+25609T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783458 | ||||||
| chr3:57783671
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+25822C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783671 | ||||||
| chr3:57783680
|
G | T | 3 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0011t0028g0133 | 3 | HG01106.hp2 HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.198+25831G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783680 | ||||||
| chr3:57783792
|
C | T | 1 | a0001c0001t0004g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.198+25943C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783792 | ||||||
| chr3:57783793
|
G | A | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+25944G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783793 | ||||||
| chr3:57783988
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+26139C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57783988 | ||||||
| chr3:57784588
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+26739C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57784588 | ||||||
| chr3:57784839
|
G | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.198+26990G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57784839 | ||||||
| chr3:57785033
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+27184A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785033 | ||||||
| chr3:57785077
|
A | G | 1 | a0001c0002t0008g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.198+27228A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785077 | ||||||
| chr3:57785247
|
T | G | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+27398T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785247 | ||||||
| chr3:57785518
|
C | T | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(8): Show | 11 | HG01934.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+27669C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785518 | ||||||
| chr3:57785633
|
A | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+27784A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785633 | ||||||
| chr3:57785650
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+27801T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785650 | ||||||
| chr3:57785742
|
C | A | 1 | a0001c0001t0002g0309 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.198+27893C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785742 | ||||||
| chr3:57785995
|
A | G | 236 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(233): Show | 236 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.198+28146A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57785995 | ||||||
| chr3:57786129
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+28280C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786129 | ||||||
| chr3:57786258
|
T | A | 3 | a0001c0001t0004g0075a0001c0001t0004g0081a0001c0002t0017g0101 | 3 | NA18940.hp1 NA18943.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.198+28409T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786258 | ||||||
| chr3:57786392
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+28543A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786392 | ||||||
| chr3:57786552
|
C | CT | 10 | a0001c0001t0001g0290a0001c0001t0005g0177a0001c0001t0005g0178others(7): Show | 10 | HG01361.hp1 HG01516.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+28724dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57786552 | |||||
| chr3:57786552
|
CT | C | 13 | a0001c0001t0001g0136a0001c0001t0002g0026a0001c0001t0002g0037others(10): Show | 13 | HG01168.hp2 HG01257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+28724delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57786552 | |||||
| chr3:57786553
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0003g0131 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.198+28704T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786553 | ||||||
| chr3:57786576
|
A | G | 2 | a0001c0006t0002g0012a0001c0006t0002g0064 | 2 | NA18949.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.198+28727A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786576 | ||||||
| chr3:57786596
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+28747A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786596 | ||||||
| chr3:57786597
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+28748T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786597 | ||||||
| chr3:57786612
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.198+28763A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786612 | ||||||
| chr3:57786731
|
A | AT | 14 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0003g0192others(11): Show | 14 | HG01099.hp2 HG01168.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+28902dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57786731 | |||||
| chr3:57786731
|
AT | A | 121 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(118): Show | 121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.198+28902delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57786731 | |||||
| chr3:57786784
|
A | C | 1 | a0001c0002t0002g0056 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.198+28935A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786784 | ||||||
| chr3:57786787
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+28938G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786787 | ||||||
| chr3:57786834
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+28985C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786834 | ||||||
| chr3:57786894
|
T | C | 1 | a0001c0001t0006g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.198+29045T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786894 | ||||||
| chr3:57786916
|
T | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+29067T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786916 | ||||||
| chr3:57786982
|
C | T | 2 | a0001c0001t0005g0152a0001c0001t0005g0183 | 2 | HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.198+29133C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57786982 | ||||||
| chr3:57787082
|
C | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+29233C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787082 | ||||||
| chr3:57787546
|
C | T | 1 | a0001c0001t0006g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.198+29697C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787546 | ||||||
| chr3:57787629
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+29780C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787629 | ||||||
| chr3:57787737
|
A | G | 26 | a0001c0001t0004g0075a0001c0001t0004g0080a0001c0001t0004g0081others(23): Show | 26 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.198+29888A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787737 | ||||||
| chr3:57787767
|
A | T | 23 | a0001c0001t0027g0246a0001c0002t0001g0201a0001c0002t0001g0202others(20): Show | 23 | HG00673.hp2 HG01928.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+29918A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787767 | ||||||
| chr3:57787866
|
A | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+30017A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787866 | ||||||
| chr3:57787921
|
A | G | 1 | a0001c0002t0002g0015 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+30072A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57787921 | ||||||
| chr3:57788295
|
TTAAG | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+30450_198+3045 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57788295 | |||||
| chr3:57788298
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+30449A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57788298 | ||||||
| chr3:57788335
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+30486A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57788335 | ||||||
| chr3:57788394
|
T | TG | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+30546dupG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57788394 | |||||
| chr3:57788612
|
G | A | 7 | a0001c0001t0036g0200a0001c0002t0001g0273a0001c0002t0008g0223others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+30763G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57788612 | ||||||
| chr3:57788832
|
C | A | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.198+30983C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57788832 | ||||||
| chr3:57788859
|
TAGGGAGT others(5): Show |
T | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.198+31025_198+3103 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57788859 | |||||
| chr3:57789101
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+31252T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789101 | ||||||
| chr3:57789241
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+31392G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789241 | ||||||
| chr3:57789282
|
G | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+31433G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789282 | ||||||
| chr3:57789451
|
A | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+31602A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789451 | ||||||
| chr3:57789468
|
C | T | 1 | a0001c0001t0014g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.198+31619C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789468 | ||||||
| chr3:57789589
|
A | G | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.198+31740A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789589 | ||||||
| chr3:57789600
|
A | G | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.198+31751A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789600 | ||||||
| chr3:57789612
|
A | G | 93 | a0001c0001t0027g0246a0001c0001t0036g0200a0001c0002t0001g0196others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.198+31763A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789612 | ||||||
| chr3:57789761
|
A | T | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.198+31912A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789761 | ||||||
| chr3:57789876
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+32027G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789876 | ||||||
| chr3:57789998
|
A | G | 243 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(240): Show | 243 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.198+32149A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57789998 | ||||||
| chr3:57790061
|
C | G | 2 | a0001c0001t0004g0081a0001c0002t0017g0101 | 2 | NA18943.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.198+32212C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790061 | ||||||
| chr3:57790424
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+32575G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790424 | ||||||
| chr3:57790481
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.198+32632A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790481 | ||||||
| chr3:57790543
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.198+32694A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790543 | ||||||
| chr3:57790670
|
G | T | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.198+32821G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790670 | ||||||
| chr3:57790681
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.198+32832G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790681 | ||||||
| chr3:57790684
|
A | G | 3 | a0001c0001t0004g0083a0001c0001t0004g0090a0001c0001t0004g0095 | 3 | NA18947.hp1 NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.198+32835A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790684 | ||||||
| chr3:57790878
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.198+33029A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57790878 | ||||||
| chr3:57791201
|
C | CA | 5 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0154others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+33361dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57791201 | |||||
| chr3:57791333
|
C | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+33484C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791333 | ||||||
| chr3:57791342
|
A | G | 2 | a0001c0001t0004g0081a0001c0002t0017g0101 | 2 | NA18943.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.198+33493A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791342 | ||||||
| chr3:57791393
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+33544T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791393 | ||||||
| chr3:57791440
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.198+33591A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791440 | ||||||
| chr3:57791749
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+33900A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791749 | ||||||
| chr3:57791970
|
G | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+34121G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57791970 | ||||||
| chr3:57792035
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+34186T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792035 | ||||||
| chr3:57792141
|
T | TAAATATT others(123): Show |
1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.198+34302_198+3430 others(134): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57792141 | |||||
| chr3:57792199
|
TG | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+34352delG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57792199 | |||||
| chr3:57792260
|
A | G | 3 | a0001c0001t0006g0103a0001c0001t0025g0003a0001c0001t0032g0004 | 3 | HG02055.hp1 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198+34411A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792260 | ||||||
| chr3:57792294
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198+34445G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792294 | ||||||
| chr3:57792529
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+34680G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792529 | ||||||
| chr3:57792536
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+34687T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792536 | ||||||
| chr3:57792876
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+35027A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792876 | ||||||
| chr3:57792907
|
C | G | 243 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(240): Show | 243 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.198+35058C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57792907 | ||||||
| chr3:57793009
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0127 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.198+35160C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793009 | ||||||
| chr3:57793056
|
T | C | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0034others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+35207T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793056 | ||||||
| chr3:57793119
|
C | CAGAGTAA others(1): Show |
124 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.198+35271_198+3527 others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57793119 | |||||
| chr3:57793315
|
A | G | 5 | a0001c0002t0001g0219a0001c0002t0001g0238a0001c0002t0001g0261others(2): Show | 5 | HG00639.hp2 HG03927.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+35466A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793315 | ||||||
| chr3:57793716
|
A | G | 2 | a0001c0001t0011g0179a0001c0001t0011g0191 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.198+35867A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793716 | ||||||
| chr3:57793831
|
G | T | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+35982G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793831 | ||||||
| chr3:57793896
|
T | TA | 16 | a0001c0001t0001g0122a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00621.hp1 HG01109.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198+36067dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57793896 | |||||
| chr3:57793896
|
TA | T | 9 | a0001c0001t0002g0033a0001c0001t0002g0050a0001c0001t0002g0306others(6): Show | 9 | HG01168.hp2 HG01346.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+36067delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57793896 | |||||
| chr3:57793943
|
T | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+36094T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793943 | ||||||
| chr3:57793947
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+36098G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57793947 | ||||||
| chr3:57794109
|
T | C | 131 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.198+36260T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794109 | ||||||
| chr3:57794196
|
T | TAGTGTGC others(203): Show |
1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.198+36359_198+3636 others(214): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57794196 | |||||
| chr3:57794196
|
T | TAGTGTGC others(241): Show |
1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+36359_198+3636 others(252): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57794196 | |||||
| chr3:57794241
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.198+36392A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794241 | ||||||
| chr3:57794252
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+36403G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794252 | ||||||
| chr3:57794284
|
A | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+36435A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794284 | ||||||
| chr3:57794347
|
T | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+36498T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794347 | ||||||
| chr3:57794555
|
A | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+36706A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794555 | ||||||
| chr3:57794672
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-36711G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57794672 | ||||||
| chr3:57795017
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-36366G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795017 | ||||||
| chr3:57795174
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.199-36209T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795174 | ||||||
| chr3:57795204
|
T | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0044 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.199-36179T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795204 | ||||||
| chr3:57795277
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-36106C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795277 | ||||||
| chr3:57795315
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-36068G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795315 | ||||||
| chr3:57795321
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-36062C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795321 | ||||||
| chr3:57795322
|
GA | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-36060delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795322 | ||||||
| chr3:57795354
|
G | A | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-36029G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795354 | ||||||
| chr3:57795366
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.199-36017C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795366 | ||||||
| chr3:57795393
|
A | C | 4 | a0001c0001t0013g0077a0001c0001t0013g0078a0001c0001t0013g0079others(1): Show | 4 | NA18980.hp2 NA18982.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-35990A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795393 | ||||||
| chr3:57795415
|
T | C | 1 | a0001c0002t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.199-35968T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795415 | ||||||
| chr3:57795674
|
T | C | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.199-35709T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795674 | ||||||
| chr3:57795679
|
A | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-35704A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795679 | ||||||
| chr3:57795712
|
G | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-35671G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795712 | ||||||
| chr3:57795737
|
C | A | 1 | a0001c0002t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.199-35646C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795737 | ||||||
| chr3:57795798
|
A | AAACACTG others(19): Show |
1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-35584_199-3555 others(30): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57795798 | |||||
| chr3:57795812
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.199-35571T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795812 | ||||||
| chr3:57795989
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-35394A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57795989 | ||||||
| chr3:57796139
|
C | G | 1 | a0001c0001t0002g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.199-35244C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796139 | ||||||
| chr3:57796182
|
G | T | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-35201G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796182 | ||||||
| chr3:57796247
|
G | A | 1 | a0001c0002t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.199-35136G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796247 | ||||||
| chr3:57796260
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-35123A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796260 | ||||||
| chr3:57796370
|
A | C | 2 | a0001c0002t0001g0204a0001c0002t0001g0206 | 2 | HG00099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.199-35013A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796370 | ||||||
| chr3:57796934
|
C | T | 3 | a0001c0002t0001g0205a0001c0002t0001g0211a0001c0002t0001g0263 | 3 | HG00280.hp1 HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.199-34449C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57796934 | ||||||
| chr3:57797013
|
C | G | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.199-34370C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797013 | ||||||
| chr3:57797018
|
A | AT | 73 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.199-34354dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57797018 | |||||
| chr3:57797183
|
T | TA | 104 | a0001c0001t0003g0125a0001c0001t0004g0075a0001c0001t0004g0086others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.199-34180dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57797183 | |||||
| chr3:57797183
|
T | TAA | 9 | a0001c0001t0014g0102a0001c0002t0001g0226a0001c0002t0001g0227others(6): Show | 9 | HG02145.hp2 NA18940.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-34181_199-3418 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57797183 | |||||
| chr3:57797453
|
C | G | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33930C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797453 | ||||||
| chr3:57797455
|
G | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33928G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797455 | ||||||
| chr3:57797460
|
G | C | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33923G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797460 | ||||||
| chr3:57797466
|
A | C | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33917A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797466 | ||||||
| chr3:57797511
|
G | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33872G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797511 | ||||||
| chr3:57797517
|
G | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33866G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797517 | ||||||
| chr3:57797522
|
G | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33861G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797522 | ||||||
| chr3:57797524
|
T | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33859T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797524 | ||||||
| chr3:57797569
|
G | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33814G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797569 | ||||||
| chr3:57797570
|
T | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33813T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797570 | ||||||
| chr3:57797619
|
T | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33764T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797619 | ||||||
| chr3:57797621
|
A | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33762A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797621 | ||||||
| chr3:57797622
|
T | C | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33761T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797622 | ||||||
| chr3:57797623
|
A | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33760A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797623 | ||||||
| chr3:57797625
|
T | A | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33758T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797625 | ||||||
| chr3:57797626
|
C | T | 1 | a0001c0001t0038g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-33757C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57797626 | ||||||
| chr3:57798007
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-33376G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798007 | ||||||
| chr3:57798092
|
A | G | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-33291A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798092 | ||||||
| chr3:57798112
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-33271T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798112 | ||||||
| chr3:57798127
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-33256G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798127 | ||||||
| chr3:57798164
|
T | C | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.199-33219T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798164 | ||||||
| chr3:57798184
|
G | T | 3 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0193 | 3 | HG02451.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.199-33199G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798184 | ||||||
| chr3:57798254
|
GCTGT | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-33124_199-3312 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57798254 | |||||
| chr3:57798369
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.199-33014T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798369 | ||||||
| chr3:57798546
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-32837C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798546 | ||||||
| chr3:57798609
|
A | G | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-32774A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798609 | ||||||
| chr3:57798740
|
T | G | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0266 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.199-32643T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798740 | ||||||
| chr3:57798928
|
T | A | 1 | a0001c0001t0004g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.199-32455T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57798928 | ||||||
| chr3:57799365
|
T | G | 7 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(4): Show | 7 | HG00544.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-32018T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799365 | ||||||
| chr3:57799379
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-32004G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799379 | ||||||
| chr3:57799387
|
T | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-31996T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799387 | ||||||
| chr3:57799450
|
T | C | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-31933T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799450 | ||||||
| chr3:57799553
|
T | A | 1 | a0001c0001t0005g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199-31830T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799553 | ||||||
| chr3:57799571
|
A | T | 21 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.199-31812A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799571 | ||||||
| chr3:57799636
|
A | G | 1 | a0001c0001t0005g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.199-31747A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799636 | ||||||
| chr3:57799797
|
C | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-31586C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57799797 | ||||||
| chr3:57800131
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-31252G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800131 | ||||||
| chr3:57800204
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-31179G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800204 | ||||||
| chr3:57800277
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-31106G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800277 | ||||||
| chr3:57800518
|
A | G | 1 | a0001c0001t0005g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.199-30865A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800518 | ||||||
| chr3:57800606
|
G | C | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-30777G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800606 | ||||||
| chr3:57800670
|
G | T | 5 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0126others(2): Show | 5 | HG00280.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-30713G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800670 | ||||||
| chr3:57800687
|
A | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-30696A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800687 | ||||||
| chr3:57800825
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-30558C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800825 | ||||||
| chr3:57800858
|
T | A | 1 | a0001c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.199-30525T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800858 | ||||||
| chr3:57800876
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.199-30507G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800876 | ||||||
| chr3:57800930
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-30453A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57800930 | ||||||
| chr3:57801034
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-30349G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801034 | ||||||
| chr3:57801114
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.199-30269A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801114 | ||||||
| chr3:57801130
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-30253T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801130 | ||||||
| chr3:57801262
|
G | A | 1 | a0001c0001t0012g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.199-30121G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801262 | ||||||
| chr3:57801283
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-30100G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801283 | ||||||
| chr3:57801342
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-30041G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801342 | ||||||
| chr3:57801349
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0001g0233 | 2 | NA18991.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.199-30034G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801349 | ||||||
| chr3:57801643
|
G | GT | 106 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.199-29727dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57801643 | |||||
| chr3:57801643
|
GT | G | 39 | a0001c0001t0002g0021a0001c0001t0002g0061a0001c0001t0003g0138others(36): Show | 39 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.199-29727delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57801643 | |||||
| chr3:57801696
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.199-29687G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801696 | ||||||
| chr3:57801801
|
TC | T | 6 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-29580delC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57801801 | |||||
| chr3:57801913
|
A | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-29470A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57801913 | ||||||
| chr3:57802155
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199-29228G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802155 | ||||||
| chr3:57802242
|
G | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-29141G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802242 | ||||||
| chr3:57802337
|
G | A | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.199-29046G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802337 | ||||||
| chr3:57802498
|
T | A | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.199-28885T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802498 | ||||||
| chr3:57802556
|
G | A | 93 | a0001c0001t0027g0246a0001c0001t0036g0200a0001c0002t0001g0196others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.199-28827G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802556 | ||||||
| chr3:57802936
|
A | G | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.199-28447A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802936 | ||||||
| chr3:57802982
|
T | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-28401T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57802982 | ||||||
| chr3:57803001
|
AGTG | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-28381_199-2837 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57803001 | ||||||
| chr3:57803094
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.199-28289A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57803094 | ||||||
| chr3:57803946
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-27437C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57803946 | ||||||
| chr3:57804039
|
T | C | 1 | a0001c0001t0007g0150 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.199-27344T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804039 | ||||||
| chr3:57804307
|
G | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-27076G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804307 | ||||||
| chr3:57804425
|
G | A | 2 | a0001c0002t0001g0234a0001c0002t0001g0272 | 2 | NA19005.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.199-26958G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804425 | ||||||
| chr3:57804555
|
G | A | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-26828G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804555 | ||||||
| chr3:57804627
|
C | G | 1 | a0001c0001t0035g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-26756C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804627 | ||||||
| chr3:57804846
|
C | T | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.199-26537C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804846 | ||||||
| chr3:57804869
|
G | A | 4 | a0001c0002t0001g0197a0001c0002t0001g0207a0001c0002t0001g0208others(1): Show | 4 | HG00733.hp1 HG00741.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-26514G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804869 | ||||||
| chr3:57804915
|
T | G | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.199-26468T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57804915 | ||||||
| chr3:57805179
|
T | C | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-26204T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805179 | ||||||
| chr3:57805343
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-26040C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805343 | ||||||
| chr3:57805395
|
T | A | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-25988T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805395 | ||||||
| chr3:57805395
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-25988T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805395 | ||||||
| chr3:57805421
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-25962A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805421 | ||||||
| chr3:57805712
|
A | T | 2 | a0001c0002t0001g0231a0001c0002t0001g0235 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.199-25671A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805712 | ||||||
| chr3:57805841
|
C | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-25542C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805841 | ||||||
| chr3:57805868
|
A | G | 1 | a0001c0001t0015g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.199-25515A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57805868 | ||||||
| chr3:57805900
|
GACTCACT others(3): Show |
G | 2 | a0001c0001t0001g0136a0001c0001t0003g0182 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.199-25477_199-2546 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57805900 | |||||
| chr3:57806019
|
G | GT | 8 | a0001c0001t0004g0075a0001c0001t0004g0094a0001c0001t0025g0003others(5): Show | 8 | HG01358.hp2 HG02055.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-25354dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57806019 | |||||
| chr3:57806021
|
T | TG | 4 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007others(1): Show | 4 | HG01934.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-25362_199-2536 others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806021 | ||||||
| chr3:57806022
|
T | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-25361T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806022 | ||||||
| chr3:57806026
|
T | G | 1 | a0001c0002t0001g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.199-25357T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806026 | ||||||
| chr3:57806044
|
T | G | 1 | a0001c0001t0005g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.199-25339T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806044 | ||||||
| chr3:57806170
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-25213A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806170 | ||||||
| chr3:57806207
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.199-25176C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806207 | ||||||
| chr3:57806364
|
C | G | 1 | a0001c0002t0001g0221 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.199-25019C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806364 | ||||||
| chr3:57806416
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-24967G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806416 | ||||||
| chr3:57806474
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.199-24909G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806474 | ||||||
| chr3:57806530
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-24853C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806530 | ||||||
| chr3:57806604
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-24779A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806604 | ||||||
| chr3:57806640
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-24743G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806640 | ||||||
| chr3:57806661
|
C | T | 1 | a0001c0002t0001g0296 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.199-24722C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806661 | ||||||
| chr3:57806691
|
C | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-24692C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806691 | ||||||
| chr3:57806800
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.199-24583A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806800 | ||||||
| chr3:57806886
|
T | C | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-24497T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57806886 | ||||||
| chr3:57807020
|
A | G | 1 | a0001c0001t0013g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.199-24363A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807020 | ||||||
| chr3:57807045
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-24338A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807045 | ||||||
| chr3:57807051
|
C | T | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.199-24332C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807051 | ||||||
| chr3:57807367
|
G | A | 1 | a0001c0001t0009g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199-24016G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807367 | ||||||
| chr3:57807870
|
G | T | 1 | a0001c0008t0005g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.199-23513G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807870 | ||||||
| chr3:57807872
|
A | G | 1 | a0001c0002t0001g0221 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.199-23511A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57807872 | ||||||
| chr3:57808053
|
G | T | 39 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(36): Show | 39 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.199-23330G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808053 | ||||||
| chr3:57808095
|
G | A | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-23288G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808095 | ||||||
| chr3:57808216
|
T | C | 1 | a0001c0002t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.199-23167T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808216 | ||||||
| chr3:57808243
|
G | A | 1 | a0001c0002t0001g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199-23140G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808243 | ||||||
| chr3:57808385
|
G | A | 1 | a0001c0001t0006g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.199-22998G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808385 | ||||||
| chr3:57808448
|
G | C | 1 | a0001c0001t0020g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.199-22935G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808448 | ||||||
| chr3:57808603
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-22780G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808603 | ||||||
| chr3:57808726
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-22657A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808726 | ||||||
| chr3:57808875
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-22508T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57808875 | ||||||
| chr3:57809071
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0044 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.199-22312C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57809071 | ||||||
| chr3:57809359
|
G | A | 3 | a0001c0002t0002g0051a0001c0002t0002g0057a0001c0002t0002g0070 | 3 | NA19004.hp1 NA19058.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.199-22024G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57809359 | ||||||
| chr3:57809527
|
A | G | 93 | a0001c0001t0027g0246a0001c0001t0036g0200a0001c0002t0001g0196others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.199-21856A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57809527 | ||||||
| chr3:57809571
|
C | T | 41 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(38): Show | 41 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.199-21812C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57809571 | ||||||
| chr3:57809572
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-21811G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57809572 | ||||||
| chr3:57810258
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.199-21125G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810258 | ||||||
| chr3:57810269
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.199-21114C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810269 | ||||||
| chr3:57810348
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-21035G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810348 | ||||||
| chr3:57810450
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-20933G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810450 | ||||||
| chr3:57810456
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-20927C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810456 | ||||||
| chr3:57810643
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-20740C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57810643 | ||||||
| chr3:57811324
|
G | C | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-20059G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57811324 | ||||||
| chr3:57811534
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.199-19849G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57811534 | ||||||
| chr3:57811729
|
C | T | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.199-19654C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57811729 | ||||||
| chr3:57811875
|
T | C | 2 | a0001c0002t0001g0251a0001c0002t0001g0253 | 2 | NA18990.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.199-19508T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57811875 | ||||||
| chr3:57812023
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-19360G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812023 | ||||||
| chr3:57812441
|
T | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.199-18942T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812441 | ||||||
| chr3:57812451
|
T | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-18932T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812451 | ||||||
| chr3:57812459
|
G | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.199-18924G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812459 | ||||||
| chr3:57812697
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-18686G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812697 | ||||||
| chr3:57812815
|
T | A | 43 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(40): Show | 43 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-18568T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812815 | ||||||
| chr3:57812936
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-18447T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57812936 | ||||||
| chr3:57813013
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.199-18370T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813013 | ||||||
| chr3:57813019
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.199-18364C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813019 | ||||||
| chr3:57813095
|
C | CT | 8 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0075others(5): Show | 8 | HG01175.hp2 HG02559.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-18270dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57813095 | |||||
| chr3:57813095
|
CT | C | 9 | a0001c0001t0001g0120a0001c0001t0002g0309a0001c0001t0005g0149others(6): Show | 9 | HG01099.hp2 HG01256.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-18270delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57813095 | |||||
| chr3:57813188
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.199-18195C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813188 | ||||||
| chr3:57813408
|
T | C | 1 | a0001c0001t0022g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.199-17975T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813408 | ||||||
| chr3:57813452
|
A | G | 308 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.199-17931A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813452 | ||||||
| chr3:57813633
|
A | C | 215 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(212): Show | 215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.199-17750A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813633 | ||||||
| chr3:57813701
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-17682G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813701 | ||||||
| chr3:57813794
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.199-17589A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813794 | ||||||
| chr3:57813901
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.199-17482T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57813901 | ||||||
| chr3:57814092
|
CT | C | 7 | a0001c0001t0002g0024a0001c0001t0002g0029a0001c0001t0005g0177others(4): Show | 7 | HG01361.hp1 HG01516.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-17278delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57814092 | |||||
| chr3:57814125
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-17258C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814125 | ||||||
| chr3:57814173
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-17210G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814173 | ||||||
| chr3:57814292
|
C | T | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-17091C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814292 | ||||||
| chr3:57814431
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-16952G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814431 | ||||||
| chr3:57814875
|
C | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-16508C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814875 | ||||||
| chr3:57814959
|
T | C | 34 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(31): Show | 34 | HG01109.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.199-16424T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57814959 | ||||||
| chr3:57815001
|
A | T | 2 | a0001c0001t0001g0136a0001c0001t0003g0182 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.199-16382A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815001 | ||||||
| chr3:57815031
|
A | G | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-16352A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815031 | ||||||
| chr3:57815044
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-16339C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815044 | ||||||
| chr3:57815237
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-16146G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815237 | ||||||
| chr3:57815250
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-16133T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815250 | ||||||
| chr3:57815448
|
G | GC | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-15931dupC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57815448 | |||||
| chr3:57815556
|
T | C | 10 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-15827T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815556 | ||||||
| chr3:57815695
|
C | T | 1 | a0001c0001t0006g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.199-15688C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815695 | ||||||
| chr3:57815833
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.199-15550C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815833 | ||||||
| chr3:57815987
|
T | G | 131 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.199-15396T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57815987 | ||||||
| chr3:57816127
|
G | GTGTT | 31 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(28): Show | 31 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.199-15226_199-1522 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57816127 | |||||
| chr3:57816127
|
GTGTT | G | 12 | a0001c0001t0002g0058a0001c0001t0004g0088a0001c0001t0010g0300others(9): Show | 12 | HG00673.hp1 HG01934.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-15226_199-1522 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57816127 | |||||
| chr3:57816335
|
G | A | 35 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(32): Show | 35 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.199-15048G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816335 | ||||||
| chr3:57816345
|
T | C | 5 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0005g0163others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-15038T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816345 | ||||||
| chr3:57816444
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-14939G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816444 | ||||||
| chr3:57816542
|
T | C | 1 | a0001c0011t0028g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.199-14841T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816542 | ||||||
| chr3:57816632
|
G | A | 2 | a0001c0006t0002g0012a0001c0006t0002g0064 | 2 | NA18949.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.199-14751G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816632 | ||||||
| chr3:57816740
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0042 | 2 | HG02083.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.199-14643T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57816740 | ||||||
| chr3:57817186
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-14197G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57817186 | ||||||
| chr3:57817212
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-14171G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57817212 | ||||||
| chr3:57817360
|
A | G | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-14023A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57817360 | ||||||
| chr3:57817874
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-13509A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57817874 | ||||||
| chr3:57818076
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.199-13307T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818076 | ||||||
| chr3:57818158
|
TTTG | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-13222_199-1322 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57818158 | |||||
| chr3:57818244
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.199-13139C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818244 | ||||||
| chr3:57818383
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0033g0305 | 2 | HG00673.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.199-13000G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818383 | ||||||
| chr3:57818447
|
G | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-12936G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818447 | ||||||
| chr3:57818514
|
G | A | 1 | a0001c0001t0022g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.199-12869G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818514 | ||||||
| chr3:57818773
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.199-12610A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818773 | ||||||
| chr3:57818822
|
T | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-12561T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818822 | ||||||
| chr3:57818824
|
T | C | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-12559T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57818824 | ||||||
| chr3:57819050
|
C | A | 1 | a0001c0002t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.199-12333C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819050 | ||||||
| chr3:57819512
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-11871A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819512 | ||||||
| chr3:57819528
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.199-11855A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819528 | ||||||
| chr3:57819545
|
A | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-11838A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819545 | ||||||
| chr3:57819731
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-11652T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819731 | ||||||
| chr3:57819790
|
T | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-11593T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819790 | ||||||
| chr3:57819828
|
C | G | 1 | a0001c0001t0009g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.199-11555C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819828 | ||||||
| chr3:57819858
|
T | G | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.199-11525T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819858 | ||||||
| chr3:57819863
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.199-11520C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57819863 | ||||||
| chr3:57820015
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-11368C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820015 | ||||||
| chr3:57820172
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199-11211A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820172 | ||||||
| chr3:57820199
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-11184G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820199 | ||||||
| chr3:57820290
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-11093G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820290 | ||||||
| chr3:57820337
|
A | G | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-11046A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820337 | ||||||
| chr3:57820559
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-10824C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820559 | ||||||
| chr3:57820562
|
G | T | 1 | a0001c0001t0004g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.199-10821G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57820562 | ||||||
| chr3:57820876
|
T | TATTG | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-10506_199-1050 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57820876 | |||||
| chr3:57821221
|
T | C | 2 | a0001c0002t0001g0234a0001c0002t0001g0272 | 2 | NA19005.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.199-10162T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821221 | ||||||
| chr3:57821281
|
A | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-10102A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821281 | ||||||
| chr3:57821357
|
G | A | 2 | a0001c0004t0002g0013a0001c0004t0002g0018 | 2 | HG02055.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.199-10026G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821357 | ||||||
| chr3:57821392
|
T | C | 3 | a0001c0001t0002g0039a0001c0001t0002g0065a0001c0001t0002g0069 | 3 | HG00438.hp1 HG02056.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.199-9991T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821392 | ||||||
| chr3:57821610
|
C | T | 6 | a0001c0001t0001g0119a0001c0002t0001g0196a0001c0002t0001g0199others(3): Show | 6 | HG01243.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-9773C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821610 | ||||||
| chr3:57821840
|
C | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0009t0031g0001 | 3 | HG02559.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.199-9543C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821840 | ||||||
| chr3:57821912
|
T | TTCC | 9 | a0001c0001t0002g0041a0001c0001t0011g0179a0001c0001t0011g0180others(6): Show | 9 | HG01099.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-9444_199-9442d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57821912 | |||||
| chr3:57821912
|
T | TTCCTCC | 127 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.199-9447_199-9442d others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57821912 | |||||
| chr3:57821912
|
T | TTCCTCCT others(5): Show |
1 | a0001c0002t0001g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.199-9453_199-9442d others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57821912 | |||||
| chr3:57821912
|
TTCCTCC | T | 4 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-9447_199-9442d others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57821912 | |||||
| chr3:57821932
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.199-9451C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57821932 | ||||||
| chr3:57822336
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0042 | 2 | HG02083.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.199-9047T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57822336 | ||||||
| chr3:57822618
|
C | G | 4 | a0001c0001t0003g0145a0001c0001t0003g0159a0001c0001t0003g0160others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-8765C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57822618 | ||||||
| chr3:57822743
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-8640C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57822743 | ||||||
| chr3:57822915
|
T | C | 4 | a0001c0002t0001g0199a0001c0002t0001g0237a0001c0002t0001g0259others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-8468T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57822915 | ||||||
| chr3:57823099
|
A | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-8284A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823099 | ||||||
| chr3:57823123
|
A | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-8260A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823123 | ||||||
| chr3:57823156
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-8227G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823156 | ||||||
| chr3:57823189
|
T | G | 22 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-8194T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823189 | ||||||
| chr3:57823248
|
T | C | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-8135T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823248 | ||||||
| chr3:57823368
|
T | C | 34 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(31): Show | 34 | HG01109.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.199-8015T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823368 | ||||||
| chr3:57823395
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-7988G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823395 | ||||||
| chr3:57823669
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199-7714G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823669 | ||||||
| chr3:57823790
|
G | A | 1 | a0001c0001t0011g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-7593G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57823790 | ||||||
| chr3:57824072
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-7311G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824072 | ||||||
| chr3:57824092
|
A | G | 1 | a0001c0001t0009g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199-7291A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824092 | ||||||
| chr3:57824184
|
TAAGTAAA others(4): Show |
T | 1 | a0001c0002t0002g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.199-7195_199-7185d others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57824184 | |||||
| chr3:57824454
|
G | T | 1 | a0001c0002t0002g0015 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.199-6929G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824454 | ||||||
| chr3:57824528
|
A | C | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.199-6855A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824528 | ||||||
| chr3:57824612
|
C | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-6771C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824612 | ||||||
| chr3:57824655
|
T | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-6728T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824655 | ||||||
| chr3:57824881
|
A | C | 1 | a0001c0002t0001g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-6502A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57824881 | ||||||
| chr3:57825221
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0003g0182 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.199-6162A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825221 | ||||||
| chr3:57825319
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-6064C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825319 | ||||||
| chr3:57825500
|
CT | C | 12 | a0001c0001t0003g0141a0001c0001t0004g0080a0001c0001t0004g0086others(9): Show | 12 | HG01257.hp2 HG02145.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-5867delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57825500 | |||||
| chr3:57825506
|
T | C | 2 | a0001c0002t0001g0218a0001c0002t0021g0239 | 2 | NA18977.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.199-5877T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825506 | ||||||
| chr3:57825525
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-5858A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825525 | ||||||
| chr3:57825639
|
A | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.199-5744A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825639 | ||||||
| chr3:57825657
|
A | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0067 | 2 | NA19007.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.199-5726A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825657 | ||||||
| chr3:57825761
|
G | A | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.199-5622G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825761 | ||||||
| chr3:57825841
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-5542G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57825841 | ||||||
| chr3:57826045
|
T | C | 1 | a0001c0002t0008g0277 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.199-5338T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826045 | ||||||
| chr3:57826121
|
G | A | 4 | a0001c0001t0004g0087a0001c0001t0004g0088a0001c0001t0004g0094others(1): Show | 4 | HG01358.hp2 HG01361.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-5262G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826121 | ||||||
| chr3:57826199
|
C | T | 1 | a0001c0001t0013g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199-5184C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826199 | ||||||
| chr3:57826321
|
A | G | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-5062A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826321 | ||||||
| chr3:57826374
|
T | G | 1 | a0001c0001t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.199-5009T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826374 | ||||||
| chr3:57826846
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-4537A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57826846 | ||||||
| chr3:57827073
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-4310A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827073 | ||||||
| chr3:57827118
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-4265A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827118 | ||||||
| chr3:57827204
|
C | A | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(121): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.199-4179C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827204 | ||||||
| chr3:57827433
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0288 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.199-3950C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827433 | ||||||
| chr3:57827464
|
A | G | 1 | a0001c0002t0008g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.199-3919A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827464 | ||||||
| chr3:57827708
|
T | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-3675T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827708 | ||||||
| chr3:57827796
|
G | T | 1 | a0001c0002t0019g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.199-3587G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57827796 | ||||||
| chr3:57827834
|
GAGA | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-3546_199-3544d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57827834 | |||||
| chr3:57828535
|
A | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-2848A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57828535 | ||||||
| chr3:57828729
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.199-2654C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57828729 | ||||||
| chr3:57828906
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.199-2477G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57828906 | ||||||
| chr3:57828997
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-2386G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57828997 | ||||||
| chr3:57829205
|
T | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2178T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829205 | ||||||
| chr3:57829443
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0040 | 2 | HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199-1940C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829443 | ||||||
| chr3:57829643
|
C | G | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.199-1740C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829643 | ||||||
| chr3:57829760
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.199-1623A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829760 | ||||||
| chr3:57829857
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-1526G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829857 | ||||||
| chr3:57829875
|
T | G | 243 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(240): Show | 243 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.199-1508T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829875 | ||||||
| chr3:57829876
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-1507C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57829876 | ||||||
| chr3:57830074
|
G | T | 1 | a0001c0001t0004g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.199-1309G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830074 | ||||||
| chr3:57830097
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.199-1286C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830097 | ||||||
| chr3:57830132
|
T | G | 3 | a0001c0002t0001g0236a0001c0002t0017g0299a0001c0002t0030g0279 | 3 | NA18939.hp2 NA18999.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.199-1251T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830132 | ||||||
| chr3:57830215
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-1168C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830215 | ||||||
| chr3:57830287
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1096C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830287 | ||||||
| chr3:57830332
|
G | T | 1 | a0001c0001t0002g0021 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.199-1051G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830332 | ||||||
| chr3:57830379
|
A | G | 11 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-1004A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830379 | ||||||
| chr3:57830425
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.199-958C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830425 | ||||||
| chr3:57830426
|
A | G | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-957A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830426 | ||||||
| chr3:57830474
|
T | C | 1 | a0001c0002t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.199-909T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830474 | ||||||
| chr3:57830486
|
G | T | 1 | a0001c0001t0010g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-897G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830486 | ||||||
| chr3:57830487
|
G | T | 1 | a0001c0001t0010g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-896G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830487 | ||||||
| chr3:57830658
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-725T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830658 | ||||||
| chr3:57830689
|
T | C | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.199-694T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830689 | ||||||
| chr3:57830696
|
C | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.199-687C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830696 | ||||||
| chr3:57830917
|
T | C | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01169.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-466T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57830917 | ||||||
| chr3:57831017
|
T | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-366T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831017 | ||||||
| chr3:57831039
|
A | G | 1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.199-344A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831039 | ||||||
| chr3:57831063
|
T | A | 2 | a0001c0002t0001g0298a0004c0010t0001g0285 | 2 | HG01168.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.199-320T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831063 | ||||||
| chr3:57831108
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-275A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831108 | ||||||
| chr3:57831148
|
T | C | 1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-235T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831148 | ||||||
| chr3:57831226
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-157A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831226 | ||||||
| chr3:57831277
|
ATTCACTT others(7): Show |
A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-103_199-90delC others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 57831277 | |||||
| chr3:57831293
|
T | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-90T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831293 | ||||||
| chr3:57831316
|
T | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0067 | 2 | NA19007.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.199-67T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 2/24 | chr3 | 57831316 | ||||||
| chr3:57831715
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.346+185G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57831715 | ||||||
| chr3:57831768
|
A | G | 39 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(36): Show | 39 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.346+238A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57831768 | ||||||
| chr3:57831855
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.346+325G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57831855 | ||||||
| chr3:57832205
|
C | T | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.346+675C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832205 | ||||||
| chr3:57832345
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.346+815G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832345 | ||||||
| chr3:57832476
|
G | T | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+946G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832476 | ||||||
| chr3:57832672
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.346+1142G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832672 | ||||||
| chr3:57832773
|
G | T | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1243G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832773 | ||||||
| chr3:57832914
|
A | G | 109 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.346+1384A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57832914 | ||||||
| chr3:57833018
|
G | C | 1 | a0001c0001t0002g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.346+1488G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833018 | ||||||
| chr3:57833090
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.346+1560C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833090 | ||||||
| chr3:57833115
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.346+1585C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833115 | ||||||
| chr3:57833262
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.346+1732C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833262 | ||||||
| chr3:57833329
|
A | G | 1 | a0001c0003t0007g0156 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.346+1799A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833329 | ||||||
| chr3:57833391
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.346+1861A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833391 | ||||||
| chr3:57833428
|
G | GT | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.346+1910dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57833428 | |||||
| chr3:57833688
|
G | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.346+2158G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833688 | ||||||
| chr3:57833790
|
T | A | 1 | a0001c0001t0003g0171 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.346+2260T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833790 | ||||||
| chr3:57833790
|
T | TA | 13 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+2273dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57833790 | |||||
| chr3:57833902
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.346+2372T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57833902 | ||||||
| chr3:57834033
|
C | G | 1 | a0001c0002t0002g0015 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.346+2503C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57834033 | ||||||
| chr3:57834393
|
A | T | 2 | a0001c0001t0015g0139a0001c0001t0015g0174 | 2 | HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.346+2863A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57834393 | ||||||
| chr3:57834581
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.346+3051A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57834581 | ||||||
| chr3:57835077
|
G | A | 1 | a0001c0001t0010g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346+3547G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835077 | ||||||
| chr3:57835121
|
C | CA | 12 | a0001c0001t0002g0042a0001c0001t0003g0129a0001c0001t0003g0130others(9): Show | 12 | HG01106.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.346+3619dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57835121 | |||||
| chr3:57835121
|
CA | C | 152 | a0001c0001t0001g0119a0001c0001t0001g0142a0001c0001t0001g0287others(149): Show | 152 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.346+3619delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57835121 | |||||
| chr3:57835121
|
CAA | C | 80 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0136others(77): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.346+3618_346+3619d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57835121 | |||||
| chr3:57835121
|
CAAA | C | 9 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(6): Show | 9 | HG00280.hp1 HG01099.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+3617_346+3619d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57835121 | |||||
| chr3:57835242
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0105 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.346+3712C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835242 | ||||||
| chr3:57835279
|
C | T | 1 | a0001c0001t0006g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.346+3749C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835279 | ||||||
| chr3:57835285
|
TG | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+3757delG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57835285 | |||||
| chr3:57835528
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.346+3998G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835528 | ||||||
| chr3:57835539
|
G | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+4009G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835539 | ||||||
| chr3:57835793
|
A | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.346+4263A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835793 | ||||||
| chr3:57835875
|
CAAAACAA others(11): Show |
C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+4346_346+4363d others(20): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835875 | ||||||
| chr3:57835998
|
A | G | 1 | a0001c0002t0008g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.346+4468A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57835998 | ||||||
| chr3:57836145
|
A | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+4615A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836145 | ||||||
| chr3:57836159
|
A | T | 6 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0051others(3): Show | 6 | NA18974.hp2 NA18984.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+4629A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836159 | ||||||
| chr3:57836308
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+4778G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836308 | ||||||
| chr3:57836677
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.347-4622C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836677 | ||||||
| chr3:57836695
|
A | G | 10 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(7): Show | 10 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-4604A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836695 | ||||||
| chr3:57836859
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-4440C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57836859 | ||||||
| chr3:57837005
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.347-4294T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837005 | ||||||
| chr3:57837039
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.347-4260A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837039 | ||||||
| chr3:57837116
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-4183A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837116 | ||||||
| chr3:57837223
|
T | G | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.347-4076T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837223 | ||||||
| chr3:57837526
|
G | C | 1 | a0001c0004t0002g0018 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.347-3773G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837526 | ||||||
| chr3:57837529
|
C | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0301 | 3 | HG02559.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.347-3770C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837529 | ||||||
| chr3:57837888
|
C | T | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-3411C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837888 | ||||||
| chr3:57837896
|
G | A | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.347-3403G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837896 | ||||||
| chr3:57837984
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-3315C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57837984 | ||||||
| chr3:57838028
|
AT | A | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3268delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57838028 | |||||
| chr3:57838157
|
C | CT | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3136dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57838157 | |||||
| chr3:57838295
|
A | G | 7 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(4): Show | 7 | HG00544.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-3004A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838295 | ||||||
| chr3:57838335
|
A | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.347-2964A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838335 | ||||||
| chr3:57838537
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.347-2762C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838537 | ||||||
| chr3:57838598
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-2701A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838598 | ||||||
| chr3:57838612
|
A | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-2687A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838612 | ||||||
| chr3:57838645
|
GA | G | 91 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.347-2653delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838645 | ||||||
| chr3:57838748
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.347-2551T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838748 | ||||||
| chr3:57838822
|
C | G | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.347-2477C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838822 | ||||||
| chr3:57838854
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-2445A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838854 | ||||||
| chr3:57838991
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-2308C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57838991 | ||||||
| chr3:57839079
|
G | A | 1 | a0001c0001t0005g0152 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.347-2220G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839079 | ||||||
| chr3:57839139
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.347-2160G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839139 | ||||||
| chr3:57839313
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-1986G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839313 | ||||||
| chr3:57839434
|
A | AT | 30 | a0001c0001t0002g0036a0001c0001t0002g0062a0001c0001t0002g0065others(27): Show | 30 | HG00741.hp1 HG01099.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.347-1841dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57839434 | |||||
| chr3:57839434
|
AT | A | 11 | a0001c0001t0002g0020a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 11 | HG00099.hp2 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1841delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57839434 | |||||
| chr3:57839495
|
C | CA | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-1803dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | 57839495 | |||||
| chr3:57839509
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-1790C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839509 | ||||||
| chr3:57839567
|
G | A | 1 | a0001c0001t0006g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-1732G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839567 | ||||||
| chr3:57839578
|
A | G | 1 | a0001c0001t0005g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.347-1721A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839578 | ||||||
| chr3:57839682
|
C | T | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.347-1617C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839682 | ||||||
| chr3:57839835
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.347-1464A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839835 | ||||||
| chr3:57839908
|
G | A | 2 | a0001c0002t0001g0219a0001c0002t0001g0234 | 2 | NA18968.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.347-1391G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57839908 | ||||||
| chr3:57840180
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-1119C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840180 | ||||||
| chr3:57840237
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.347-1062A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840237 | ||||||
| chr3:57840245
|
T | G | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.347-1054T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840245 | ||||||
| chr3:57840380
|
A | G | 158 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.347-919A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840380 | ||||||
| chr3:57840384
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.347-915T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840384 | ||||||
| chr3:57840406
|
G | C | 1 | a0001c0001t0022g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347-893G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840406 | ||||||
| chr3:57840633
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-666G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840633 | ||||||
| chr3:57840633
|
G | C | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.347-666G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840633 | ||||||
| chr3:57840658
|
G | A | 2 | a0001c0001t0004g0091a0001c0001t0004g0107 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.347-641G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57840658 | ||||||
| chr3:57841127
|
G | A | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(121): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.347-172G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57841127 | ||||||
| chr3:57841157
|
A | G | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.347-142A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 3/24 | chr3 | 57841157 | ||||||
| chr3:57841444
|
G | A | 15 | a0001c0001t0004g0075a0001c0001t0004g0081a0001c0001t0004g0083others(12): Show | 15 | HG02056.hp2 HG02132.hp1 HG03688.hp2 others(12): Show |
intron_variant | MODIFIER | c.419+73G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57841444 | ||||||
| chr3:57841472
|
A | G | 1 | a0001c0001t0005g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.419+101A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57841472 | ||||||
| chr3:57841538
|
A | G | 3 | a0001c0002t0001g0205a0001c0002t0001g0211a0001c0002t0001g0263 | 3 | HG00280.hp1 HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.419+167A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57841538 | ||||||
| chr3:57841859
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0017 | 2 | NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.419+488A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57841859 | ||||||
| chr3:57842277
|
G | T | 31 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.419+906G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842277 | ||||||
| chr3:57842278
|
T | G | 31 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.419+907T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842278 | ||||||
| chr3:57842413
|
C | T | 1 | a0001c0002t0001g0236 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.419+1042C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842413 | ||||||
| chr3:57842518
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.419+1147C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842518 | ||||||
| chr3:57842745
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.419+1374G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842745 | ||||||
| chr3:57842862
|
C | T | 1 | a0001c0001t0010g0303 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.419+1491C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57842862 | ||||||
| chr3:57843075
|
T | A | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(121): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.419+1704T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843075 | ||||||
| chr3:57843134
|
G | A | 1 | a0001c0002t0008g0277 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.419+1763G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843134 | ||||||
| chr3:57843202
|
TAGTA | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.419+1836_419+1839d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843202 | |||||
| chr3:57843257
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.419+1886C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843257 | ||||||
| chr3:57843305
|
C | CT | 26 | a0001c0001t0004g0075a0001c0001t0004g0080a0001c0001t0004g0081others(23): Show | 26 | HG01175.hp2 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.419+1958dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843305
|
C | CTT | 18 | a0001c0001t0004g0076a0001c0001t0004g0086a0001c0001t0004g0092others(15): Show | 18 | HG00408.hp1 HG00639.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.419+1957_419+1958d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843305
|
C | CTTT | 90 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.419+1956_419+1958d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843305
|
C | CTTTT | 10 | a0001c0001t0001g0288a0001c0001t0001g0292a0001c0001t0001g0294others(7): Show | 10 | HG02080.hp2 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.419+1955_419+1958d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843305
|
CTTTTTTT | C | 57 | a0001c0001t0001g0136a0001c0001t0002g0010a0001c0001t0002g0014others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.419+1952_419+1958d others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843305
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0030others(19): Show | 22 | HG00609.hp1 HG01934.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.419+1951_419+1958d others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843305 | |||||
| chr3:57843365
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+1994G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843365 | ||||||
| chr3:57843375
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+2004C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843375 | ||||||
| chr3:57843540
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.419+2169A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843540 | ||||||
| chr3:57843580
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+2209A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843580 | ||||||
| chr3:57843639
|
T | C | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.419+2268T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843639 | ||||||
| chr3:57843693
|
T | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0048 | 3 | HG02080.hp1 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.419+2322T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843693 | ||||||
| chr3:57843704
|
TTTTC | T | 108 | a0001c0001t0001g0120a0001c0001t0001g0287a0001c0001t0001g0288others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.419+2349_419+2352d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843704 | |||||
| chr3:57843706
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.419+2335T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843706 | ||||||
| chr3:57843707
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.419+2336T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843707 | ||||||
| chr3:57843708
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.419+2337C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843708 | ||||||
| chr3:57843720
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.419+2349C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843720 | ||||||
| chr3:57843722
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.419+2351T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843722 | ||||||
| chr3:57843766
|
C | T | 4 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0252others(1): Show | 4 | HG00673.hp2 HG02040.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+2395C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843766 | ||||||
| chr3:57843767
|
T | TC | 4 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0252others(1): Show | 4 | HG00673.hp2 HG02040.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+2396_419+2397i others(3): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843767 | ||||||
| chr3:57843775
|
C | CT | 87 | a0001c0001t0001g0291a0001c0001t0002g0010a0001c0001t0002g0011others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.419+2426dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843775 | |||||
| chr3:57843775
|
C | CTT | 99 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0287others(96): Show | 99 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.419+2425_419+2426d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843775 | |||||
| chr3:57843775
|
C | CTTT | 10 | a0001c0001t0001g0119a0001c0001t0001g0292a0001c0001t0001g0294others(7): Show | 10 | HG01243.hp1 HG02027.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.419+2424_419+2426d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843775 | |||||
| chr3:57843775
|
CT | C | 7 | a0001c0001t0001g0136a0001c0001t0003g0138a0001c0001t0003g0182others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.419+2426delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57843775 | |||||
| chr3:57843836
|
G | A | 2 | a0001c0004t0002g0013a0001c0004t0002g0018 | 2 | HG02055.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.419+2465G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843836 | ||||||
| chr3:57843883
|
T | C | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+2512T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843883 | ||||||
| chr3:57843900
|
C | T | 1 | a0001c0001t0005g0152 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.419+2529C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57843900 | ||||||
| chr3:57844082
|
AC | A | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.419+2713delC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57844082 | |||||
| chr3:57844125
|
G | C | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.419+2754G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844125 | ||||||
| chr3:57844171
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.419+2800T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844171 | ||||||
| chr3:57844219
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419+2848C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844219 | ||||||
| chr3:57844222
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.419+2851G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844222 | ||||||
| chr3:57844231
|
A | T | 1 | a0001c0002t0001g0242 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.419+2860A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844231 | ||||||
| chr3:57844265
|
G | A | 2 | a0001c0001t0013g0077a0001c0001t0013g0097 | 2 | NA18980.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.419+2894G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844265 | ||||||
| chr3:57844350
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420-2847G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844350 | ||||||
| chr3:57844406
|
T | A | 1 | a0001c0001t0009g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.420-2791T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844406 | ||||||
| chr3:57844452
|
C | T | 3 | a0001c0001t0006g0113a0001c0001t0006g0114a0001c0001t0006g0115 | 3 | HG00544.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.420-2745C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844452 | ||||||
| chr3:57844487
|
C | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.420-2710C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844487 | ||||||
| chr3:57844670
|
TA | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.420-2517delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57844670 | |||||
| chr3:57844711
|
CT | C | 222 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(219): Show | 222 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.420-2466delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57844711 | |||||
| chr3:57844770
|
G | A | 309 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.420-2427G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844770 | ||||||
| chr3:57844902
|
A | G | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.420-2295A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57844902 | ||||||
| chr3:57845103
|
C | T | 1 | a0001c0001t0004g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.420-2094C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845103 | ||||||
| chr3:57845135
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.420-2062T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845135 | ||||||
| chr3:57845314
|
G | A | 1 | a0001c0001t0011g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.420-1883G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845314 | ||||||
| chr3:57845483
|
C | T | 1 | a0001c0001t0011g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420-1714C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845483 | ||||||
| chr3:57845484
|
A | G | 233 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(230): Show | 233 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.420-1713A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845484 | ||||||
| chr3:57845526
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.420-1671C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845526 | ||||||
| chr3:57845613
|
G | A | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.420-1584G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845613 | ||||||
| chr3:57845705
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.420-1492C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845705 | ||||||
| chr3:57845755
|
C | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.420-1442C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845755 | ||||||
| chr3:57845799
|
A | G | 1 | a0001c0002t0001g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.420-1398A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845799 | ||||||
| chr3:57845897
|
A | C | 1 | a0001c0002t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.420-1300A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57845897 | ||||||
| chr3:57846028
|
G | T | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.420-1169G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846028 | ||||||
| chr3:57846408
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.420-789G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846408 | ||||||
| chr3:57846478
|
T | G | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.420-719T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846478 | ||||||
| chr3:57846554
|
A | AT | 23 | a0001c0001t0002g0021a0001c0001t0002g0195a0001c0001t0003g0008others(20): Show | 23 | HG00639.hp2 HG01934.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.420-623dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57846554 | |||||
| chr3:57846554
|
AT | A | 11 | a0001c0001t0001g0290a0001c0001t0002g0030a0001c0001t0006g0113others(8): Show | 11 | HG00099.hp2 HG00544.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.420-623delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | 57846554 | |||||
| chr3:57846609
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.420-588T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846609 | ||||||
| chr3:57846618
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.420-579G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846618 | ||||||
| chr3:57846639
|
C | T | 1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.420-558C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57846639 | ||||||
| chr3:57847013
|
G | C | 1 | a0001c0001t0006g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.420-184G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57847013 | ||||||
| chr3:57847013
|
G | T | 1 | a0001c0001t0002g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.420-184G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57847013 | ||||||
| chr3:57847019
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.420-178A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57847019 | ||||||
| chr3:57847096
|
C | T | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.420-101C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 4/24 | chr3 | 57847096 | ||||||
| chr3:57847362
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.456+129A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847362 | ||||||
| chr3:57847374
|
T | C | 1 | a0001c0002t0001g0219 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.456+141T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847374 | ||||||
| chr3:57847574
|
A | G | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.456+341A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847574 | ||||||
| chr3:57847659
|
C | G | 1 | a0001c0001t0003g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456+426C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847659 | ||||||
| chr3:57847677
|
C | G | 1 | a0001c0001t0003g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.456+444C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847677 | ||||||
| chr3:57847699
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.456+466T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847699 | ||||||
| chr3:57847770
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.456+537C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847770 | ||||||
| chr3:57847820
|
C | A | 1 | a0001c0001t0027g0246 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.456+587C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847820 | ||||||
| chr3:57847840
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.456+607A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847840 | ||||||
| chr3:57847972
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.456+739G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57847972 | ||||||
| chr3:57848039
|
G | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.456+806G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848039 | ||||||
| chr3:57848213
|
T | G | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.456+980T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848213 | ||||||
| chr3:57848269
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.456+1036C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848269 | ||||||
| chr3:57848272
|
A | C | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.456+1039A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848272 | ||||||
| chr3:57848424
|
C | T | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.456+1191C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848424 | ||||||
| chr3:57848442
|
G | C | 1 | a0001c0001t0003g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456+1209G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848442 | ||||||
| chr3:57848513
|
TCTTCTTC others(10): Show |
T | 3 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0048 | 3 | HG02080.hp1 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.457-1229_457-1213d others(19): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 57848513 | |||||
| chr3:57848581
|
GCTCCCTC others(2): Show |
G | 93 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.457-1170_457-1162d others(11): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 57848581 | |||||
| chr3:57848592
|
T | C | 1 | a0001c0002t0017g0299 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.457-1162T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848592 | ||||||
| chr3:57848604
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.457-1150C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848604 | ||||||
| chr3:57848632
|
C | T | 1 | a0001c0001t0035g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.457-1122C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848632 | ||||||
| chr3:57848709
|
C | CT | 110 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.457-1026dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 57848709 | |||||
| chr3:57848709
|
C | CTT | 108 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.457-1027_457-1026d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 57848709 | |||||
| chr3:57848853
|
G | T | 1 | a0001c0002t0019g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.457-901G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848853 | ||||||
| chr3:57848888
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.457-866T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57848888 | ||||||
| chr3:57849068
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.457-686C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849068 | ||||||
| chr3:57849109
|
G | A | 1 | a0001c0001t0006g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.457-645G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849109 | ||||||
| chr3:57849180
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.457-574C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849180 | ||||||
| chr3:57849303
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.457-451A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849303 | ||||||
| chr3:57849595
|
A | G | 1 | a0001c0001t0005g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.457-159A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849595 | ||||||
| chr3:57849688
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.457-66A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 5/24 | chr3 | 57849688 | ||||||
| chr3:57849866
|
T | C | 1 | a0001c0001t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.519+50T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57849866 | ||||||
| chr3:57849921
|
C | A | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.519+105C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57849921 | ||||||
| chr3:57849939
|
C | G | 1 | a0001c0001t0003g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.519+123C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57849939 | ||||||
| chr3:57849974
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.519+158G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57849974 | ||||||
| chr3:57850018
|
T | A | 10 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(7): Show | 10 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+202T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850018 | ||||||
| chr3:57850092
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.519+276C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850092 | ||||||
| chr3:57850381
|
T | G | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.519+565T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850381 | ||||||
| chr3:57850698
|
A | G | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.519+882A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850698 | ||||||
| chr3:57850729
|
G | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.519+913G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850729 | ||||||
| chr3:57850752
|
G | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.519+936G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57850752 | ||||||
| chr3:57851001
|
G | A | 1 | a0001c0002t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.519+1185G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851001 | ||||||
| chr3:57851221
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.519+1405T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851221 | ||||||
| chr3:57851246
|
T | C | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.519+1430T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851246 | ||||||
| chr3:57851352
|
G | GT | 8 | a0001c0001t0002g0021a0001c0001t0002g0066a0001c0001t0002g0195others(5): Show | 8 | HG01891.hp2 HG01978.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+1551dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57851352 | |||||
| chr3:57851352
|
G | GTT | 30 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(27): Show | 30 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.519+1550_519+1551d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57851352 | |||||
| chr3:57851352
|
G | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+1536G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851352 | ||||||
| chr3:57851352
|
GT | G | 125 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.519+1551delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57851352 | |||||
| chr3:57851405
|
T | C | 1 | a0001c0001t0006g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.519+1589T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851405 | ||||||
| chr3:57851477
|
G | GT | 7 | a0001c0001t0003g0188a0001c0001t0015g0139a0001c0001t0025g0003others(4): Show | 7 | HG00408.hp1 HG01175.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+1674dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57851477 | |||||
| chr3:57851483
|
T | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.519+1667T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851483 | ||||||
| chr3:57851533
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.519+1717C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851533 | ||||||
| chr3:57851553
|
A | G | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.519+1737A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851553 | ||||||
| chr3:57851565
|
C | T | 2 | a0001c0001t0003g0130a0001c0011t0028g0133 | 2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.519+1749C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851565 | ||||||
| chr3:57851639
|
A | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.519+1823A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851639 | ||||||
| chr3:57851697
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.519+1881C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851697 | ||||||
| chr3:57851728
|
A | G | 1 | a0001c0001t0020g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.519+1912A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851728 | ||||||
| chr3:57851760
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+1944C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851760 | ||||||
| chr3:57851823
|
C | G | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+2007C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851823 | ||||||
| chr3:57851824
|
T | A | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+2008T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851824 | ||||||
| chr3:57851825
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+2009T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851825 | ||||||
| chr3:57851827
|
T | A | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+2011T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57851827 | ||||||
| chr3:57852129
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+2313C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852129 | ||||||
| chr3:57852162
|
T | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+2346T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852162 | ||||||
| chr3:57852543
|
T | A | 1 | a0001c0001t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.519+2727T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852543 | ||||||
| chr3:57852740
|
G | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519+2924G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852740 | ||||||
| chr3:57852748
|
A | G | 70 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.519+2932A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852748 | ||||||
| chr3:57852779
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.519+2963A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852779 | ||||||
| chr3:57852889
|
A | T | 1 | a0001c0002t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.519+3073A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852889 | ||||||
| chr3:57852894
|
A | G | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.519+3078A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57852894 | ||||||
| chr3:57853330
|
T | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+3514T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853330 | ||||||
| chr3:57853786
|
A | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.520-3947A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853786 | ||||||
| chr3:57853873
|
G | A | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3860G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853873 | ||||||
| chr3:57853896
|
A | G | 1 | a0001c0001t0004g0095 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.520-3837A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853896 | ||||||
| chr3:57853941
|
C | CA | 28 | a0001c0001t0001g0120a0001c0001t0001g0289a0001c0001t0001g0292others(25): Show | 28 | HG00099.hp2 HG00733.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.520-3779dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853941 | |||||
| chr3:57853953
|
AATTATAT others(4): Show |
A | 1 | a0001c0001t0018g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.520-3777_520-3767d others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853953 | |||||
| chr3:57853953
|
AATTATAT others(10): Show |
A | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.520-3777_520-3761d others(19): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853953 | |||||
| chr3:57853954
|
A | AATT | 27 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0291others(24): Show | 27 | HG01257.hp2 HG01361.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.520-3779_520-3778i others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | AATTAT | 26 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0290others(23): Show | 26 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.520-3779_520-3778i others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | AATTATAT others(4): Show |
4 | a0001c0001t0004g0075a0001c0001t0020g0099a0001c0002t0001g0225others(1): Show | 4 | HG03688.hp2 HG04204.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3779_520-3778i others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | AATTATAT others(6): Show |
3 | a0001c0001t0004g0084a0001c0001t0036g0200a0004c0010t0001g0285 | 3 | HG01168.hp1 NA18943.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.520-3779_520-3778i others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | AATTATAT others(8): Show |
3 | a0001c0002t0001g0211a0001c0002t0001g0224a0001c0002t0001g0252 | 3 | HG00735.hp2 HG01074.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.520-3779_520-3778i others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | AATTTTAT others(4): Show |
1 | a0001c0001t0010g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-3779_520-3778i others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853954
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0182 | 2 | HG01891.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.520-3779A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853954 | ||||||
| chr3:57853955
|
T | A | 125 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0287others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.520-3778T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853955 | ||||||
| chr3:57853955
|
T | TTA | 39 | a0001c0001t0001g0142a0001c0001t0002g0021a0001c0001t0002g0022others(36): Show | 39 | HG00544.hp2 HG00609.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.520-3734_520-3733d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATA | 16 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0043others(13): Show | 16 | HG01109.hp1 HG01243.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-3736_520-3733d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATATA | 9 | a0001c0001t0002g0025a0001c0001t0002g0036a0001c0001t0002g0065others(6): Show | 9 | HG01255.hp2 HG01891.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-3738_520-3733d others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0003g0168 | 3 | HG00438.hp1 HG02630.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.520-3740_520-3733d others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.520-3742_520-3733d others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.520-3744_520-3733d others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0002g0014 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.520-3748_520-3733d others(18): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTA | T | 11 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0048others(8): Show | 11 | HG00735.hp1 HG02040.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-3734_520-3733d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATA | T | 6 | a0001c0001t0003g0159a0001c0001t0003g0173a0001c0001t0005g0147others(3): Show | 6 | HG01496.hp1 HG02280.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-3736_520-3733d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATA | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0050a0001c0001t0002g0072 | 3 | NA18977.hp1 NA18981.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.520-3738_520-3733d others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(1): Show |
T | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0304others(4): Show | 7 | HG00099.hp1 HG02523.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-3740_520-3733d others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0001g0119a0001c0001t0002g0030a0001c0001t0002g0053others(2): Show | 5 | HG01243.hp1 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-3742_520-3733d others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(5): Show |
T | 3 | a0001c0001t0003g0123a0001c0001t0003g0127a0001c0001t0003g0131 | 3 | HG00280.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.520-3744_520-3733d others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(7): Show |
T | 2 | a0001c0001t0002g0058a0001c0001t0006g0114 | 2 | HG00673.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.520-3746_520-3733d others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0002g0031a0001c0001t0003g0126a0001c0001t0037g0071 | 3 | HG00408.hp2 HG01074.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.520-3748_520-3733d others(18): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0005g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.520-3752_520-3733d others(22): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853955
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0002g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.520-3756_520-3733d others(26): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853955 | |||||
| chr3:57853956
|
T | A | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.520-3777T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TA | T | 5 | a0001c0001t0004g0091a0001c0002t0001g0205a0001c0002t0001g0206others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-3776delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATA | T | 15 | a0001c0001t0004g0083a0001c0001t0004g0093a0001c0001t0004g0104others(12): Show | 15 | HG00741.hp2 HG01175.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-3776_520-3774d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATA | T | 8 | a0001c0001t0001g0295a0001c0001t0004g0087a0001c0001t0025g0003others(5): Show | 8 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3776_520-3772d others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATATA | T | 11 | a0001c0002t0001g0215a0001c0002t0001g0217a0001c0002t0001g0227others(8): Show | 11 | HG00609.hp2 HG02080.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-3776_520-3770d others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3776_520-3762d others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-3776_520-3760d others(19): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATATA others(12): Show |
T | 2 | a0001c0001t0003g0008a0001c0001t0004g0088 | 2 | HG02559.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.520-3776_520-3758d others(21): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853956
|
TATATATA others(22): Show |
T | 1 | a0001c0001t0004g0090 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.520-3776_520-3748d others(31): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853956 | ||||||
| chr3:57853957
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.520-3776A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853957 | ||||||
| chr3:57853959
|
A | T | 4 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0035g0132others(1): Show | 4 | HG01106.hp2 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3774A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853959 | ||||||
| chr3:57853961
|
A | T | 5 | a0001c0001t0003g0125a0001c0001t0003g0129a0001c0001t0011g0180others(2): Show | 5 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-3772A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853961 | ||||||
| chr3:57853963
|
A | T | 2 | a0001c0001t0011g0179a0001c0001t0011g0191 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.520-3770A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853963 | ||||||
| chr3:57853965
|
A | T | 1 | a0001c0001t0018g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.520-3768A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853965 | ||||||
| chr3:57853967
|
A | G | 5 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0005g0163others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-3766A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853967 | ||||||
| chr3:57853968
|
TATATATA others(68): Show |
T | 5 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0005g0163others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-3764_520-3690d others(77): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853968 | ||||||
| chr3:57853969
|
A | T | 1 | a0001c0001t0003g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.520-3764A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853969 | ||||||
| chr3:57853971
|
A | T | 4 | a0001c0001t0003g0123a0001c0001t0003g0127a0001c0001t0003g0131others(1): Show | 4 | HG00280.hp2 HG01261.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3762A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853971 | ||||||
| chr3:57853973
|
A | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0293 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.520-3760A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853973 | ||||||
| chr3:57853975
|
A | T | 1 | a0001c0001t0003g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.520-3758A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853975 | ||||||
| chr3:57853976
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0293 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.520-3757T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57853976 | ||||||
| chr3:57853978
|
TATATATA others(24): Show |
T | 1 | a0001c0001t0015g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.520-3746_520-3716d others(33): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853978 | |||||
| chr3:57853999
|
AT | A | 3 | a0001c0002t0001g0257a0001c0002t0001g0261a0001c0002t0001g0278 | 3 | HG01169.hp1 HG03927.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.520-3731delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57853999 | |||||
| chr3:57854033
|
ATG | A | 72 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-3696_520-3695d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57854033 | |||||
| chr3:57854037
|
G | GTA | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3687_520-3686d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57854037 | |||||
| chr3:57854068
|
T | TTA | 226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.520-3653_520-3652d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57854068 | |||||
| chr3:57854068
|
T | TTATA | 3 | a0001c0001t0014g0102a0001c0002t0001g0215a0001c0002t0001g0229 | 3 | HG02145.hp2 NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.520-3655_520-3652d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57854068 | |||||
| chr3:57854115
|
A | G | 35 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(32): Show | 35 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.520-3618A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854115 | ||||||
| chr3:57854269
|
A | G | 7 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(4): Show | 7 | HG00544.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-3464A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854269 | ||||||
| chr3:57854324
|
C | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0230 | 2 | HG00408.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.520-3409C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854324 | ||||||
| chr3:57854334
|
TG | T | 308 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.520-3397delG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57854334 | |||||
| chr3:57854384
|
G | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3349G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854384 | ||||||
| chr3:57854520
|
C | T | 1 | a0001c0002t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.520-3213C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854520 | ||||||
| chr3:57854523
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3210G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854523 | ||||||
| chr3:57854646
|
G | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3087G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854646 | ||||||
| chr3:57854773
|
T | C | 1 | a0001c0008t0005g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.520-2960T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854773 | ||||||
| chr3:57854913
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-2820C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57854913 | ||||||
| chr3:57855144
|
G | A | 31 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(28): Show | 31 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.520-2589G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855144 | ||||||
| chr3:57855205
|
C | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.520-2528C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855205 | ||||||
| chr3:57855271
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.520-2462G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855271 | ||||||
| chr3:57855275
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.520-2458G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855275 | ||||||
| chr3:57855320
|
G | A | 2 | a0002c0005t0001g0213a0002c0005t0001g0265 | 2 | NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.520-2413G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855320 | ||||||
| chr3:57855325
|
C | A | 1 | a0001c0001t0006g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.520-2408C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855325 | ||||||
| chr3:57855514
|
G | T | 1 | a0001c0002t0002g0056 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.520-2219G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855514 | ||||||
| chr3:57855596
|
G | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-2137G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855596 | ||||||
| chr3:57855670
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.520-2063G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855670 | ||||||
| chr3:57855711
|
T | TA | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0075others(32): Show | 35 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.520-2008dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57855711 | |||||
| chr3:57855711
|
T | TAA | 20 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0287others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.520-2009_520-2008d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57855711 | |||||
| chr3:57855711
|
T | TAAA | 76 | a0001c0001t0001g0120a0001c0001t0009g0118a0001c0001t0012g0109others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.520-2010_520-2008d others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57855711 | |||||
| chr3:57855711
|
T | TAAAA | 20 | a0001c0001t0001g0136a0001c0001t0002g0046a0001c0002t0001g0197others(17): Show | 20 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.520-2011_520-2008d others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57855711 | |||||
| chr3:57855726
|
C | A | 114 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.520-2007C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855726 | ||||||
| chr3:57855726
|
C | CA | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-1996dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57855726 | |||||
| chr3:57855734
|
A | C | 1 | a0001c0001t0002g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.520-1999A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855734 | ||||||
| chr3:57855760
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-1973G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855760 | ||||||
| chr3:57855999
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-1734C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57855999 | ||||||
| chr3:57856000
|
G | A | 1 | a0001c0002t0008g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.520-1733G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856000 | ||||||
| chr3:57856050
|
GA | G | 9 | a0001c0001t0003g0182a0001c0001t0003g0192a0001c0001t0006g0113others(6): Show | 9 | HG00544.hp2 HG01099.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.520-1670delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | 57856050 | |||||
| chr3:57856069
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.520-1664T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856069 | ||||||
| chr3:57856131
|
G | A | 29 | a0001c0001t0005g0135a0001c0001t0005g0137a0001c0001t0005g0147others(26): Show | 29 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.520-1602G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856131 | ||||||
| chr3:57856234
|
A | G | 2 | a0001c0001t0005g0149a0001c0001t0005g0157 | 2 | HG01255.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.520-1499A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856234 | ||||||
| chr3:57856477
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.520-1256G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856477 | ||||||
| chr3:57856664
|
TG | T | 3 | a0001c0001t0014g0082a0001c0001t0014g0098a0001c0001t0014g0102 | 3 | HG01257.hp2 HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.520-1068delG | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856664 | ||||||
| chr3:57856973
|
T | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-760T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57856973 | ||||||
| chr3:57857023
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.520-710T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857023 | ||||||
| chr3:57857030
|
A | G | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.520-703A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857030 | ||||||
| chr3:57857226
|
C | G | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.520-507C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857226 | ||||||
| chr3:57857387
|
A | G | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-346A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857387 | ||||||
| chr3:57857465
|
A | T | 1 | a0001c0001t0006g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.520-268A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857465 | ||||||
| chr3:57857687
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.520-46A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 6/24 | chr3 | 57857687 | ||||||
| chr3:57857834
|
C | T | 1 | a0001c0002t0001g0262 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.615+6C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 7/24 | chr3 | 57857834 | ||||||
| chr3:57857948
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.615+120G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 7/24 | chr3 | 57857948 | ||||||
| chr3:57857987
|
T | C | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.616-101T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 7/24 | chr3 | 57857987 | ||||||
| chr3:57858030
|
T | C | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0266 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.616-58T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 7/24 | chr3 | 57858030 | ||||||
| chr3:57858364
|
A | G | 40 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(37): Show | 40 | HG01109.hp2 HG01175.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.687+205A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57858364 | ||||||
| chr3:57858444
|
T | A | 1 | a0001c0002t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.687+285T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57858444 | ||||||
| chr3:57858854
|
A | G | 30 | a0001c0001t0003g0141a0001c0001t0005g0135a0001c0001t0005g0137others(27): Show | 30 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.687+695A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57858854 | ||||||
| chr3:57858998
|
C | T | 1 | a0001c0001t0003g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687+839C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57858998 | ||||||
| chr3:57859150
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.687+991C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859150 | ||||||
| chr3:57859185
|
A | G | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0009t0031g0001 | 3 | HG02559.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.687+1026A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859185 | ||||||
| chr3:57859245
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.687+1086C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859245 | ||||||
| chr3:57859246
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.687+1087G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859246 | ||||||
| chr3:57859320
|
C | CA | 16 | a0001c0001t0001g0293a0001c0001t0002g0065a0001c0001t0002g0304others(13): Show | 16 | HG01243.hp2 HG01346.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.687+1180dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr3 | 57859320 | |||||
| chr3:57859320
|
CA | C | 47 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0075others(44): Show | 47 | HG01175.hp1 HG01257.hp2 HG01433.hp2 others(44): Show |
intron_variant | MODIFIER | c.687+1180delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr3 | 57859320 | |||||
| chr3:57859341
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.687+1182C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859341 | ||||||
| chr3:57859546
|
C | A | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.688-1153C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859546 | ||||||
| chr3:57859562
|
A | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.688-1137A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859562 | ||||||
| chr3:57859654
|
C | T | 5 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0126others(2): Show | 5 | HG00280.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-1045C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859654 | ||||||
| chr3:57859713
|
G | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.688-986G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859713 | ||||||
| chr3:57859786
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-913C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859786 | ||||||
| chr3:57859853
|
G | C | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.688-846G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57859853 | ||||||
| chr3:57860081
|
T | G | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.688-618T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57860081 | ||||||
| chr3:57860243
|
G | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.688-456G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57860243 | ||||||
| chr3:57860307
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.688-392A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57860307 | ||||||
| chr3:57860426
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.688-273A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 8/24 | chr3 | 57860426 | ||||||
| chr3:57860850
|
C | A | 82 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.828+11C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57860850 | ||||||
| chr3:57860979
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.828+140C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57860979 | ||||||
| chr3:57861123
|
GT | G | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.828+285delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861123 | ||||||
| chr3:57861213
|
C | T | 2 | a0001c0001t0005g0135a0001c0001t0023g0158 | 2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.828+374C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861213 | ||||||
| chr3:57861368
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.828+529T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861368 | ||||||
| chr3:57861586
|
G | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-363G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861586 | ||||||
| chr3:57861616
|
A | T | 1 | a0001c0001t0015g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.829-333A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861616 | ||||||
| chr3:57861657
|
A | G | 1 | a0001c0001t0002g0019 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.829-292A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861657 | ||||||
| chr3:57861723
|
C | T | 1 | a0001c0001t0010g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.829-226C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861723 | ||||||
| chr3:57861796
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.829-153T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861796 | ||||||
| chr3:57861934
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.829-15A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 9/24 | chr3 | 57861934 | ||||||
| chr3:57862297
|
G | A | 1 | a0001c0001t0022g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.966+211G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862297 | ||||||
| chr3:57862377
|
C | T | 1 | a0001c0001t0020g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.966+291C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862377 | ||||||
| chr3:57862444
|
C | A | 1 | a0001c0001t0034g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.966+358C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862444 | ||||||
| chr3:57862608
|
A | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.966+522A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862608 | ||||||
| chr3:57862615
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.966+529C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862615 | ||||||
| chr3:57862616
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.966+530G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862616 | ||||||
| chr3:57862638
|
C | CA | 90 | a0001c0001t0002g0014a0001c0001t0002g0017a0001c0001t0002g0019others(87): Show | 90 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.966+574dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr3 | 57862638 | |||||
| chr3:57862638
|
C | CAA | 36 | a0001c0001t0001g0289a0001c0001t0002g0010a0001c0001t0002g0011others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.966+573_966+574dup others(2): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr3 | 57862638 | |||||
| chr3:57862638
|
C | CAAA | 105 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0136others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.966+572_966+574dup others(3): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr3 | 57862638 | |||||
| chr3:57862638
|
C | CAAAA | 13 | a0001c0001t0001g0120a0001c0001t0001g0288a0001c0001t0001g0292others(10): Show | 13 | HG01256.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.966+571_966+574dup others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr3 | 57862638 | |||||
| chr3:57862959
|
G | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+873G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57862959 | ||||||
| chr3:57863569
|
A | G | 123 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.967-979A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57863569 | ||||||
| chr3:57863582
|
T | C | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.967-966T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57863582 | ||||||
| chr3:57863674
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.967-874C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57863674 | ||||||
| chr3:57864129
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.967-419C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57864129 | ||||||
| chr3:57864321
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.967-227C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 10/24 | chr3 | 57864321 | ||||||
| chr3:57864931
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1186+74A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 12/24 | chr3 | 57864931 | ||||||
| chr3:57864944
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+87A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 12/24 | chr3 | 57864944 | ||||||
| chr3:57865004
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192 | 3 | HG01891.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1186+147A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 12/24 | chr3 | 57865004 | ||||||
| chr3:57865328
|
A | G | 4 | a0001c0002t0001g0201a0001c0002t0001g0224a0001c0002t0001g0231others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+36A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57865328 | ||||||
| chr3:57865641
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1237+349A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57865641 | ||||||
| chr3:57865741
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1237+449G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57865741 | ||||||
| chr3:57865799
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237+507C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57865799 | ||||||
| chr3:57865985
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1237+693C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57865985 | ||||||
| chr3:57866163
|
G | C | 237 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1237+871G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866163 | ||||||
| chr3:57866273
|
AAAAAG | A | 114 | a0001c0001t0001g0142a0001c0001t0003g0123a0001c0001t0003g0124others(111): Show | 114 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.1237+1003_1237+100 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57866273 | |||||
| chr3:57866273
|
AAAAAGAA others(3): Show |
A | 2 | a0001c0001t0002g0052a0001c0001t0006g0113 | 2 | HG00544.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1237+998_1237+1007 others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57866273 | |||||
| chr3:57866278
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+986G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866278 | ||||||
| chr3:57866283
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1237+991G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866283 | ||||||
| chr3:57866426
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1237+1134A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866426 | ||||||
| chr3:57866492
|
ATATGTAA others(6): Show |
A | 1 | a0001c0002t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1237+1202_1237+121 others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57866492 | |||||
| chr3:57866501
|
G | T | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1237+1209G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866501 | ||||||
| chr3:57866513
|
T | G | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01169.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237+1221T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866513 | ||||||
| chr3:57866620
|
A | T | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1237+1328A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866620 | ||||||
| chr3:57866632
|
G | A | 1 | a0001c0001t0012g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1237+1340G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866632 | ||||||
| chr3:57866700
|
T | C | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1237+1408T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866700 | ||||||
| chr3:57866726
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1237+1434T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57866726 | ||||||
| chr3:57866874
|
C | CA | 10 | a0001c0001t0002g0010a0001c0001t0004g0106a0001c0001t0010g0300others(7): Show | 10 | HG00673.hp2 HG02293.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237+1595dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57866874 | |||||
| chr3:57867438
|
G | C | 93 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1237+2146G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57867438 | ||||||
| chr3:57867770
|
A | G | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1237+2478A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57867770 | ||||||
| chr3:57867928
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1237+2636G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57867928 | ||||||
| chr3:57867965
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+2673C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57867965 | ||||||
| chr3:57868292
|
A | C | 1 | a0001c0002t0001g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1237+3000A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868292 | ||||||
| chr3:57868302
|
T | C | 10 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237+3010T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868302 | ||||||
| chr3:57868405
|
C | T | 7 | a0001c0002t0001g0212a0001c0002t0001g0226a0001c0002t0001g0227others(4): Show | 7 | HG00621.hp2 NA18944.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+3113C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868405 | ||||||
| chr3:57868429
|
T | A | 5 | a0001c0001t0002g0065a0001c0001t0012g0109a0001c0001t0012g0110others(2): Show | 5 | HG02056.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+3137T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868429 | ||||||
| chr3:57868460
|
A | G | 1 | a0001c0001t0011g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1237+3168A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868460 | ||||||
| chr3:57868559
|
T | A | 1 | a0001c0001t0006g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1238-3077T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868559 | ||||||
| chr3:57868706
|
A | C | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1238-2930A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868706 | ||||||
| chr3:57868753
|
C | G | 6 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0228others(3): Show | 6 | NA18944.hp1 NA18962.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-2883C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868753 | ||||||
| chr3:57868795
|
A | AAT | 22 | a0001c0001t0003g0138a0001c0001t0003g0159a0001c0001t0003g0167others(19): Show | 22 | HG01361.hp1 HG01516.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1238-2815_1238-281 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868795 | |||||
| chr3:57868795
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1238-2823_1238-281 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868795 | |||||
| chr3:57868795
|
AATATAT | A | 5 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0003g0192others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-2819_1238-281 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868795 | |||||
| chr3:57868795
|
AATATATA others(1): Show |
A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1238-2821_1238-281 others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868795 | |||||
| chr3:57868821
|
T | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1238-2815T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868821 | ||||||
| chr3:57868836
|
T | A | 1 | a0001c0001t0003g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1238-2800T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57868836 | ||||||
| chr3:57868859
|
TTA | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1238-2771_1238-277 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868859 | |||||
| chr3:57868935
|
TTATATGT others(15): Show |
T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0034others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-2673_1238-265 others(26): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868935 | |||||
| chr3:57868998
|
A | ATTATATA others(22): Show |
1 | a0001c0001t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1238-2637_1238-260 others(33): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57868998 | |||||
| chr3:57869138
|
G | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0009t0031g0001 | 3 | HG02559.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1238-2498G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869138 | ||||||
| chr3:57869372
|
A | G | 1 | a0001c0002t0001g0264 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1238-2264A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869372 | ||||||
| chr3:57869630
|
T | TATATATA others(12): Show |
1 | a0001c0001t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1238-2006_1238-200 others(23): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869630 | ||||||
| chr3:57869630
|
T | TTA | 33 | a0001c0001t0001g0142a0001c0001t0002g0014a0001c0001t0003g0123others(30): Show | 33 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1238-1977_1238-197 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATA | 15 | a0001c0001t0003g0125a0001c0001t0004g0080a0001c0001t0004g0087others(12): Show | 15 | HG00735.hp1 HG01071.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1238-1979_1238-197 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATA | 40 | a0001c0001t0005g0148a0001c0001t0005g0154a0001c0001t0005g0166others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1238-1981_1238-197 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(1): Show |
28 | a0001c0001t0001g0136a0001c0001t0003g0182a0001c0001t0005g0147others(25): Show | 28 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1238-1983_1238-197 others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(3): Show |
12 | a0001c0002t0001g0218a0001c0002t0001g0219a0001c0002t0001g0238others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1238-1985_1238-197 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0002t0001g0207others(2): Show | 5 | HG02622.hp1 HG02896.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-1987_1238-197 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(7): Show |
8 | a0001c0001t0001g0295a0001c0001t0002g0017a0001c0001t0002g0049others(5): Show | 8 | HG03130.hp1 HG03831.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1238-1989_1238-197 others(18): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(9): Show |
19 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0294others(16): Show | 19 | HG00438.hp1 HG01074.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1238-1991_1238-197 others(20): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(11): Show |
29 | a0001c0001t0001g0122a0001c0001t0001g0289a0001c0001t0001g0293others(26): Show | 29 | HG00609.hp1 HG01106.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.1238-1993_1238-197 others(22): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(13): Show |
9 | a0001c0001t0001g0288a0001c0001t0002g0023a0001c0001t0002g0024others(6): Show | 9 | HG00621.hp1 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1238-1995_1238-197 others(24): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(15): Show |
7 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0042others(4): Show | 7 | HG00673.hp1 HG01993.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238-1997_1238-197 others(26): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(17): Show |
5 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0043others(2): Show | 5 | HG02647.hp2 NA18980.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-1999_1238-197 others(28): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(19): Show |
3 | a0001c0001t0002g0195a0001c0001t0002g0304a0001c0002t0002g0016 | 3 | HG01978.hp1 NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1238-2001_1238-197 others(30): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0002g0021 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1238-2005_1238-197 others(34): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATAT others(25): Show |
1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1238-1976_1238-197 others(36): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTATATGT others(21): Show |
1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1238-2001_1238-200 others(32): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTTTATAT others(3): Show |
2 | a0001c0002t0001g0231a0001c0002t0001g0235 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1238-2005_1238-200 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
T | TTTTATAT others(7): Show |
2 | a0001c0002t0001g0201a0001c0002t0001g0224 | 2 | HG01074.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1238-2005_1238-200 others(18): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
TTA | T | 13 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(10): Show | 13 | HG01069.hp2 HG01175.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1238-1977_1238-197 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
TTATA | T | 3 | a0001c0001t0001g0120a0001c0001t0003g0009a0001c0001t0025g0003 | 3 | HG02630.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1238-1979_1238-197 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0002g0019 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1238-1985_1238-197 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869630
|
TTATATAT others(5): Show |
T | 7 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(4): Show | 7 | HG01109.hp2 HG01934.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1238-1987_1238-197 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869630 | |||||
| chr3:57869633
|
T | TATATATA others(20): Show |
1 | a0001c0001t0003g0171 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1238-1993_1238-196 others(31): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869633 | |||||
| chr3:57869638
|
A | AT | 3 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0186 | 3 | HG01243.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1238-1997dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869638 | |||||
| chr3:57869643
|
T | TATATATA others(6): Show |
3 | a0001c0001t0011g0179a0001c0001t0011g0181a0001c0001t0011g0191 | 3 | HG01099.hp2 HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1238-1992_1238-198 others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869643 | |||||
| chr3:57869645
|
T | TATATATA others(4): Show |
1 | a0001c0001t0011g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1238-1990_1238-198 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869645 | |||||
| chr3:57869649
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1238-1977_1238-196 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | 57869649 | |||||
| chr3:57869660
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0037g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1238-1976_1238-197 others(22): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869660 | ||||||
| chr3:57869660
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0038 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1238-1976_1238-197 others(23): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869660 | ||||||
| chr3:57869661
|
A | T | 1 | a0001c0001t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1238-1975A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869661 | ||||||
| chr3:57869662
|
T | A | 1 | a0001c0001t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1238-1974T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869662 | ||||||
| chr3:57869869
|
A | G | 1 | a0001c0001t0020g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1238-1767A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869869 | ||||||
| chr3:57869922
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0017 | 2 | NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1238-1714A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869922 | ||||||
| chr3:57869974
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1238-1662A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57869974 | ||||||
| chr3:57870104
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1238-1532T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870104 | ||||||
| chr3:57870566
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1238-1070A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870566 | ||||||
| chr3:57870670
|
C | T | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(121): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1238-966C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870670 | ||||||
| chr3:57870697
|
C | T | 33 | a0001c0001t0003g0192a0001c0001t0004g0075a0001c0001t0004g0076others(30): Show | 33 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.1238-939C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870697 | ||||||
| chr3:57870698
|
G | A | 1 | a0001c0001t0011g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1238-938G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870698 | ||||||
| chr3:57870749
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-887C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870749 | ||||||
| chr3:57870879
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1238-757A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870879 | ||||||
| chr3:57870959
|
C | G | 2 | a0001c0001t0001g0142a0001c0001t0003g0144 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1238-677C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57870959 | ||||||
| chr3:57871189
|
C | T | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1238-447C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57871189 | ||||||
| chr3:57871210
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1238-426A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57871210 | ||||||
| chr3:57871236
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1238-400C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57871236 | ||||||
| chr3:57871314
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0042 | 2 | HG02083.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1238-322A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57871314 | ||||||
| chr3:57871454
|
A | C | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1238-182A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 13/24 | chr3 | 57871454 | ||||||
| chr3:57871712
|
A | G | 5 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0154others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300+14A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57871712 | ||||||
| chr3:57871955
|
T | G | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1300+257T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57871955 | ||||||
| chr3:57871979
|
A | C | 1 | a0001c0002t0001g0250 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1300+281A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57871979 | ||||||
| chr3:57872196
|
G | C | 1 | a0001c0002t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1300+498G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872196 | ||||||
| chr3:57872256
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+558C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872256 | ||||||
| chr3:57872337
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1300+639G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872337 | ||||||
| chr3:57872373
|
T | C | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1300+675T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872373 | ||||||
| chr3:57872496
|
A | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1300+798A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872496 | ||||||
| chr3:57872985
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300+1287C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57872985 | ||||||
| chr3:57873096
|
A | T | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1300+1398A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873096 | ||||||
| chr3:57873374
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300+1676A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873374 | ||||||
| chr3:57873401
|
T | G | 160 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1300+1703T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873401 | ||||||
| chr3:57873451
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1300+1753C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873451 | ||||||
| chr3:57873481
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1300+1783C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873481 | ||||||
| chr3:57873486
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1300+1788G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873486 | ||||||
| chr3:57873498
|
G | A | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.1300+1800G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873498 | ||||||
| chr3:57873713
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300+2015C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873713 | ||||||
| chr3:57873782
|
T | G | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1300+2084T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873782 | ||||||
| chr3:57873891
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1300+2193C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873891 | ||||||
| chr3:57873937
|
A | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300+2239A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57873937 | ||||||
| chr3:57874072
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1300+2374A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874072 | ||||||
| chr3:57874145
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1300+2447A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874145 | ||||||
| chr3:57874206
|
C | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300+2508C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874206 | ||||||
| chr3:57874241
|
A | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+2543A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874241 | ||||||
| chr3:57874313
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1300+2615A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874313 | ||||||
| chr3:57874446
|
T | C | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.1300+2748T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874446 | ||||||
| chr3:57874480
|
G | T | 1 | a0001c0002t0001g0218 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1300+2782G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874480 | ||||||
| chr3:57874592
|
G | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300+2894G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874592 | ||||||
| chr3:57874625
|
C | T | 23 | a0001c0001t0005g0137a0001c0001t0005g0147a0001c0001t0005g0148others(20): Show | 23 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1300+2927C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874625 | ||||||
| chr3:57874755
|
A | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300+3057A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57874755 | ||||||
| chr3:57874859
|
C | CA | 7 | a0001c0001t0002g0055a0001c0001t0003g0176a0001c0001t0013g0078others(4): Show | 7 | HG02027.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300+3176dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57874859 | |||||
| chr3:57875220
|
T | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300+3522T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875220 | ||||||
| chr3:57875328
|
C | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300+3630C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875328 | ||||||
| chr3:57875378
|
G | A | 1 | a0001c0001t0004g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1300+3680G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875378 | ||||||
| chr3:57875382
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1300+3684A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875382 | ||||||
| chr3:57875397
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1300+3699C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875397 | ||||||
| chr3:57875575
|
C | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0034others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+3877C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875575 | ||||||
| chr3:57875868
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1300+4170A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875868 | ||||||
| chr3:57875959
|
T | G | 236 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(233): Show | 236 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1300+4261T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57875959 | ||||||
| chr3:57876243
|
A | G | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1300+4545A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57876243 | ||||||
| chr3:57876403
|
T | G | 1 | a0001c0002t0002g0070 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1300+4705T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57876403 | ||||||
| chr3:57876604
|
T | A | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1300+4906T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57876604 | ||||||
| chr3:57876696
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300+4998A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57876696 | ||||||
| chr3:57877013
|
G | A | 278 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1300+5315G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877013 | ||||||
| chr3:57877613
|
T | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+5915T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877613 | ||||||
| chr3:57877635
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1300+5937A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877635 | ||||||
| chr3:57877640
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+5942G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877640 | ||||||
| chr3:57877690
|
G | C | 1 | a0001c0002t0001g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1300+5992G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877690 | ||||||
| chr3:57877708
|
T | A | 1 | a0001c0002t0001g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1300+6010T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877708 | ||||||
| chr3:57877831
|
C | CT | 21 | a0001c0001t0001g0142a0001c0001t0002g0011a0001c0001t0002g0022others(18): Show | 21 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1300+6155dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57877831 | |||||
| chr3:57877831
|
C | CTTT | 32 | a0001c0001t0002g0036a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300+6153_1300+615 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57877831 | |||||
| chr3:57877831
|
CT | C | 12 | a0001c0001t0003g0124a0001c0001t0003g0170a0001c0001t0005g0147others(9): Show | 12 | HG01255.hp2 HG01256.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1300+6155delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57877831 | |||||
| chr3:57877854
|
A | T | 2 | a0001c0001t0004g0086a0001c0001t0012g0110 | 2 | HG02735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1300+6156A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877854 | ||||||
| chr3:57877855
|
A | T | 2 | a0001c0001t0004g0086a0001c0001t0012g0110 | 2 | HG02735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1300+6157A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877855 | ||||||
| chr3:57877857
|
C | A | 2 | a0001c0001t0004g0086a0001c0001t0012g0110 | 2 | HG02735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1300+6159C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877857 | ||||||
| chr3:57877857
|
CAG | C | 34 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(31): Show | 34 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1300+6162_1300+616 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57877857 | |||||
| chr3:57877859
|
G | C | 2 | a0001c0001t0004g0086a0001c0001t0012g0110 | 2 | HG02735.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1300+6161G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877859 | ||||||
| chr3:57877865
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1300+6167C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877865 | ||||||
| chr3:57877905
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300+6207A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57877905 | ||||||
| chr3:57878089
|
T | C | 280 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1300+6391T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878089 | ||||||
| chr3:57878271
|
G | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1300+6573G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878271 | ||||||
| chr3:57878594
|
T | C | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1300+6896T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878594 | ||||||
| chr3:57878762
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1300+7064A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878762 | ||||||
| chr3:57878922
|
G | A | 278 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1300+7224G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878922 | ||||||
| chr3:57878977
|
G | A | 4 | a0001c0001t0003g0145a0001c0001t0003g0159a0001c0001t0003g0160others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+7279G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57878977 | ||||||
| chr3:57879035
|
T | C | 123 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1300+7337T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879035 | ||||||
| chr3:57879041
|
C | T | 1 | a0001c0001t0005g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1300+7343C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879041 | ||||||
| chr3:57879430
|
T | C | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1300+7732T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879430 | ||||||
| chr3:57879463
|
A | G | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1300+7765A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879463 | ||||||
| chr3:57879613
|
G | A | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1300+7915G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879613 | ||||||
| chr3:57879767
|
C | T | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+8069C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879767 | ||||||
| chr3:57879956
|
A | T | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+8258A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879956 | ||||||
| chr3:57879957
|
A | AT | 110 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1300+8259_1300+826 others(5): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879957 | ||||||
| chr3:57879957
|
A | T | 9 | a0001c0001t0002g0029a0001c0001t0002g0042a0001c0001t0006g0074others(6): Show | 9 | HG00544.hp2 HG02083.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1300+8259A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879957 | ||||||
| chr3:57879958
|
A | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1300+8260A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879958 | ||||||
| chr3:57879963
|
T | A | 1 | a0001c0001t0005g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1300+8265T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879963 | ||||||
| chr3:57879969
|
T | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1300+8271T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879969 | ||||||
| chr3:57879970
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300+8272A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57879970 | ||||||
| chr3:57880021
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1300+8323T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880021 | ||||||
| chr3:57880112
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1300+8414C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880112 | ||||||
| chr3:57880169
|
T | TTTTTG | 32 | a0001c0001t0002g0309a0001c0001t0003g0123a0001c0001t0003g0128others(29): Show | 32 | HG00544.hp2 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300+8514_1300+851 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880169
|
T | TTTTTGTT others(3): Show |
6 | a0001c0001t0003g0009a0001c0001t0005g0137a0001c0001t0022g0134others(3): Show | 6 | HG03453.hp1 HG03831.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300+8509_1300+851 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880169
|
TTTTTG | T | 20 | a0001c0001t0001g0293a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 20 | HG01074.hp2 HG01099.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1300+8514_1300+851 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880169
|
TTTTTGTT others(3): Show |
T | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1300+8509_1300+851 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880169
|
TTTTTGTT others(8): Show |
T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300+8504_1300+851 others(19): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880169
|
TTTTTGTT others(13): Show |
T | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1300+8499_1300+851 others(24): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57880169 | |||||
| chr3:57880449
|
C | T | 2 | a0001c0001t0004g0076a0001c0001t0004g0092 | 2 | HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1300+8751C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880449 | ||||||
| chr3:57880564
|
T | A | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1300+8866T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880564 | ||||||
| chr3:57880568
|
G | A | 1 | a0001c0008t0005g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1300+8870G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880568 | ||||||
| chr3:57880625
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+8927C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880625 | ||||||
| chr3:57880651
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1300+8953G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880651 | ||||||
| chr3:57880775
|
C | T | 70 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1300+9077C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880775 | ||||||
| chr3:57880778
|
G | A | 1 | a0001c0001t0002g0038 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1300+9080G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57880778 | ||||||
| chr3:57881065
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1301-8976G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881065 | ||||||
| chr3:57881094
|
T | C | 3 | a0001c0001t0004g0083a0001c0001t0004g0090a0001c0001t0004g0095 | 3 | NA18947.hp1 NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1301-8947T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881094 | ||||||
| chr3:57881120
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-8921G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881120 | ||||||
| chr3:57881239
|
A | G | 3 | a0001c0001t0004g0085a0001c0001t0004g0089a0001c0001t0027g0246 | 3 | HG02056.hp2 HG02132.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1301-8802A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881239 | ||||||
| chr3:57881289
|
TATC | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1301-8749_1301-874 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57881289 | |||||
| chr3:57881369
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1301-8672A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881369 | ||||||
| chr3:57881456
|
T | G | 1 | a0001c0006t0002g0064 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1301-8585T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881456 | ||||||
| chr3:57881521
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1301-8520G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881521 | ||||||
| chr3:57881583
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1301-8458G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881583 | ||||||
| chr3:57881609
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1301-8432C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881609 | ||||||
| chr3:57881749
|
C | T | 1 | a0001c0002t0019g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1301-8292C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881749 | ||||||
| chr3:57881975
|
C | G | 1 | a0001c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1301-8066C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57881975 | ||||||
| chr3:57882007
|
T | TTAAA | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG00741.hp2 HG01934.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301-8012_1301-800 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57882007 | |||||
| chr3:57882007
|
TTAAATAA others(5): Show |
T | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1301-8020_1301-800 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57882007 | |||||
| chr3:57882102
|
T | C | 10 | a0001c0001t0001g0122a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301-7939T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882102 | ||||||
| chr3:57882250
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1301-7791A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882250 | ||||||
| chr3:57882317
|
T | C | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1301-7724T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882317 | ||||||
| chr3:57882378
|
A | C | 1 | a0001c0001t0006g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1301-7663A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882378 | ||||||
| chr3:57882427
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1301-7614A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882427 | ||||||
| chr3:57882931
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1301-7110T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57882931 | ||||||
| chr3:57883191
|
C | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1301-6850C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57883191 | ||||||
| chr3:57883372
|
A | G | 2 | a0001c0001t0004g0094a0001c0001t0004g0108 | 2 | HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1301-6669A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57883372 | ||||||
| chr3:57883937
|
C | CT | 7 | a0001c0001t0003g0141a0001c0001t0003g0189a0001c0001t0005g0161others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1301-6088dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57883937 | |||||
| chr3:57883937
|
CT | C | 193 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1301-6088delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57883937 | |||||
| chr3:57884023
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1301-6018G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884023 | ||||||
| chr3:57884148
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1301-5893C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884148 | ||||||
| chr3:57884236
|
T | C | 121 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1301-5805T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884236 | ||||||
| chr3:57884263
|
G | T | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1301-5778G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884263 | ||||||
| chr3:57884587
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1301-5454T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884587 | ||||||
| chr3:57884753
|
G | A | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1301-5288G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884753 | ||||||
| chr3:57884796
|
C | G | 2 | a0002c0005t0001g0213a0002c0005t0001g0265 | 2 | NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1301-5245C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884796 | ||||||
| chr3:57884818
|
T | A | 3 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0262 | 3 | HG00099.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1301-5223T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884818 | ||||||
| chr3:57884835
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1301-5206A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884835 | ||||||
| chr3:57884844
|
A | G | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1301-5197A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884844 | ||||||
| chr3:57884885
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1301-5156G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57884885 | ||||||
| chr3:57885034
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1301-5007G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885034 | ||||||
| chr3:57885041
|
G | A | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1301-5000G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885041 | ||||||
| chr3:57885071
|
A | AT | 73 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0017others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1301-4952dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885071 | |||||
| chr3:57885071
|
AT | A | 7 | a0001c0001t0003g0170a0001c0001t0011g0179a0001c0001t0011g0180others(4): Show | 7 | HG00639.hp1 HG01099.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1301-4952delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885071 | |||||
| chr3:57885153
|
AC | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1301-4886delC | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885153 | |||||
| chr3:57885174
|
G | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-4867G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885174 | ||||||
| chr3:57885175
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-4866C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885175 | ||||||
| chr3:57885376
|
TTTG | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-4650_1301-464 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885376 | |||||
| chr3:57885423
|
G | GT | 30 | a0001c0001t0003g0128a0001c0001t0003g0138a0001c0001t0003g0141others(27): Show | 30 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1301-4604dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885423 | |||||
| chr3:57885423
|
GT | G | 223 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(220): Show | 223 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1301-4604delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885423 | |||||
| chr3:57885481
|
G | A | 2 | a0001c0001t0012g0109a0001c0001t0012g0111 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1301-4560G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885481 | ||||||
| chr3:57885505
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-4536C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885505 | ||||||
| chr3:57885625
|
G | T | 1 | a0001c0001t0005g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1301-4416G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885625 | ||||||
| chr3:57885760
|
G | T | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1301-4281G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885760 | ||||||
| chr3:57885771
|
C | CT | 6 | a0001c0001t0003g0125a0001c0001t0003g0141a0001c0001t0005g0135others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1301-4240dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0012g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1301-4261_1301-424 others(26): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0012g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1301-4263_1301-424 others(28): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0014g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1301-4265_1301-424 others(30): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CT | C | 53 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0142others(50): Show | 53 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1301-4240delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTT | C | 85 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0287others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1301-4241_1301-424 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTT | C | 8 | a0001c0001t0001g0293a0001c0001t0009g0116a0001c0001t0009g0117others(5): Show | 8 | HG00408.hp1 HG01069.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1301-4242_1301-424 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0014 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1301-4249_1301-424 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(4): Show |
C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0017others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1301-4250_1301-424 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(5): Show |
C | 25 | a0001c0001t0004g0075a0001c0001t0004g0080a0001c0001t0004g0081others(22): Show | 25 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1301-4251_1301-424 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0290a0001c0001t0025g0003 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1301-4255_1301-424 others(20): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-4256_1301-424 others(21): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885771
|
CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1301-4257_1301-424 others(22): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57885771 | |||||
| chr3:57885927
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1301-4114G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885927 | ||||||
| chr3:57885928
|
C | T | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1301-4113C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57885928 | ||||||
| chr3:57886106
|
A | AT | 158 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0136others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1301-3920dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57886106 | |||||
| chr3:57886184
|
A | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1301-3857A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886184 | ||||||
| chr3:57886205
|
G | A | 4 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-3836G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886205 | ||||||
| chr3:57886288
|
G | A | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1301-3753G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886288 | ||||||
| chr3:57886399
|
T | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301-3642T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886399 | ||||||
| chr3:57886911
|
G | T | 1 | a0001c0001t0003g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1301-3130G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886911 | ||||||
| chr3:57886980
|
A | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1301-3061A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57886980 | ||||||
| chr3:57887033
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1301-3008G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57887033 | ||||||
| chr3:57887235
|
A | AT | 39 | a0001c0001t0002g0073a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 39 | HG00280.hp1 HG00735.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1301-2789dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57887235 | |||||
| chr3:57887235
|
A | T | 1 | a0001c0002t0001g0296 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1301-2806A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57887235 | ||||||
| chr3:57887235
|
AT | A | 17 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(14): Show | 17 | HG01069.hp2 HG01168.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1301-2789delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57887235 | |||||
| chr3:57887495
|
A | G | 4 | a0001c0001t0003g0145a0001c0001t0003g0159a0001c0001t0003g0160others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-2546A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57887495 | ||||||
| chr3:57887759
|
C | A | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-2282C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57887759 | ||||||
| chr3:57887918
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1301-2123A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57887918 | ||||||
| chr3:57888092
|
T | C | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1301-1949T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888092 | ||||||
| chr3:57888125
|
G | A | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1301-1916G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888125 | ||||||
| chr3:57888126
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0288 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1301-1915A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888126 | ||||||
| chr3:57888206
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1301-1835T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888206 | ||||||
| chr3:57888426
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1301-1615G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888426 | ||||||
| chr3:57888434
|
T | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-1607T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888434 | ||||||
| chr3:57888730
|
AAT | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-1309_1301-130 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57888730 | |||||
| chr3:57888763
|
G | T | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1301-1278G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888763 | ||||||
| chr3:57888834
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1301-1207A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888834 | ||||||
| chr3:57888875
|
G | A | 1 | a0001c0001t0004g0085 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1301-1166G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888875 | ||||||
| chr3:57888902
|
T | G | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1301-1139T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57888902 | ||||||
| chr3:57888905
|
GT | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301-1127delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 57888905 | |||||
| chr3:57889010
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1301-1031G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889010 | ||||||
| chr3:57889312
|
T | G | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1301-729T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889312 | ||||||
| chr3:57889517
|
A | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1301-524A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889517 | ||||||
| chr3:57889658
|
A | G | 23 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0229others(20): Show | 23 | HG00673.hp2 HG01928.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1301-383A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889658 | ||||||
| chr3:57889857
|
G | A | 3 | a0001c0002t0001g0236a0001c0002t0017g0299a0001c0002t0030g0279 | 3 | NA18939.hp2 NA18999.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1301-184G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889857 | ||||||
| chr3:57889860
|
A | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301-181A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57889860 | ||||||
| chr3:57890029
|
T | C | 1 | a0001c0001t0004g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1301-12T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 14/24 | chr3 | 57890029 | ||||||
| chr3:57890204
|
T | C | 5 | a0001c0002t0001g0196a0001c0002t0001g0199a0001c0002t0001g0237others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+104T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890204 | ||||||
| chr3:57890281
|
C | T | 1 | a0001c0001t0014g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1360+181C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890281 | ||||||
| chr3:57890440
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1360+340A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890440 | ||||||
| chr3:57890594
|
T | C | 1 | a0001c0002t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1360+494T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890594 | ||||||
| chr3:57890927
|
A | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1360+827A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890927 | ||||||
| chr3:57890976
|
G | A | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.1360+876G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57890976 | ||||||
| chr3:57891117
|
A | G | 1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1360+1017A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891117 | ||||||
| chr3:57891206
|
G | GA | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+1120dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57891206 | |||||
| chr3:57891206
|
GA | G | 7 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0002g0040others(4): Show | 7 | HG00280.hp2 HG02293.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1360+1120delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57891206 | |||||
| chr3:57891260
|
T | C | 32 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(29): Show | 32 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1360+1160T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891260 | ||||||
| chr3:57891490
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360+1390C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891490 | ||||||
| chr3:57891551
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+1451A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891551 | ||||||
| chr3:57891577
|
C | CT | 38 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(35): Show | 38 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1360+1489dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57891577 | |||||
| chr3:57891598
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1360+1498C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891598 | ||||||
| chr3:57891722
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1360+1622G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891722 | ||||||
| chr3:57891790
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1360+1690T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891790 | ||||||
| chr3:57891820
|
ACCCGCCT others(1249): Show |
A | 2 | a0001c0002t0001g0221a0001c0002t0019g0220 | 2 | HG02735.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1360+1753_1360+300 others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57891820 | |||||
| chr3:57891889
|
C | T | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1360+1789C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891889 | ||||||
| chr3:57891996
|
A | T | 1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1360+1896A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57891996 | ||||||
| chr3:57892053
|
A | G | 1 | a0001c0001t0004g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1360+1953A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892053 | ||||||
| chr3:57892055
|
A | G | 1 | a0001c0001t0010g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1360+1955A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892055 | ||||||
| chr3:57892231
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1360+2131T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892231 | ||||||
| chr3:57892237
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1360+2137A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892237 | ||||||
| chr3:57892238
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1360+2138T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892238 | ||||||
| chr3:57892349
|
C | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1360+2249C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892349 | ||||||
| chr3:57892387
|
A | G | 1 | a0001c0001t0003g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1360+2287A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892387 | ||||||
| chr3:57892783
|
A | AAC | 16 | a0001c0001t0001g0293a0001c0001t0003g0124a0001c0001t0004g0080others(13): Show | 16 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1360+2709_1360+271 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892783 | |||||
| chr3:57892783
|
A | AACAC | 29 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0081others(26): Show | 29 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1360+2707_1360+271 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892783 | |||||
| chr3:57892783
|
A | AACACAC | 4 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0014g0102others(1): Show | 4 | HG02145.hp2 HG02698.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360+2705_1360+271 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892783 | |||||
| chr3:57892783
|
AACAC | A | 9 | a0001c0001t0002g0061a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02559.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360+2707_1360+271 others(8): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892783 | |||||
| chr3:57892783
|
AACACACA others(5): Show |
A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360+2699_1360+271 others(16): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892783 | |||||
| chr3:57892811
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1360+2711T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892811 | ||||||
| chr3:57892831
|
CT | C | 262 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1360+2750delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57892831 | |||||
| chr3:57892905
|
C | T | 3 | a0001c0001t0015g0139a0001c0001t0015g0174a0001c0001t0015g0175 | 3 | HG01255.hp2 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1360+2805C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892905 | ||||||
| chr3:57892932
|
T | C | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(121): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1360+2832T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57892932 | ||||||
| chr3:57893053
|
T | C | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1360+2953T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893053 | ||||||
| chr3:57893331
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-3180C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893331 | ||||||
| chr3:57893445
|
GA | G | 121 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(118): Show | 121 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1361-3053delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57893445 | |||||
| chr3:57893448
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1361-3063A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893448 | ||||||
| chr3:57893682
|
T | C | 1 | a0001c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1361-2829T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893682 | ||||||
| chr3:57893709
|
C | CCTTTTGT others(31): Show |
1 | a0001c0001t0001g0290 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1361-2771_1361-277 others(42): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57893709 | |||||
| chr3:57893852
|
G | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-2659G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893852 | ||||||
| chr3:57893884
|
T | G | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1361-2627T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893884 | ||||||
| chr3:57893894
|
G | A | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-2617G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57893894 | ||||||
| chr3:57894193
|
T | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1361-2318T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57894193 | ||||||
| chr3:57894204
|
C | A | 1 | a0001c0001t0005g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1361-2307C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57894204 | ||||||
| chr3:57894207
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1361-2304A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57894207 | ||||||
| chr3:57894281
|
T | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-2230T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57894281 | ||||||
| chr3:57894617
|
A | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1361-1894A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57894617 | ||||||
| chr3:57895027
|
C | T | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1361-1484C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895027 | ||||||
| chr3:57895159
|
A | G | 3 | a0001c0002t0001g0232a0001c0002t0001g0245a0001c0002t0001g0260 | 3 | HG01928.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1361-1352A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895159 | ||||||
| chr3:57895160
|
G | A | 1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1361-1351G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895160 | ||||||
| chr3:57895160
|
G | C | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1361-1351G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895160 | ||||||
| chr3:57895336
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1361-1175T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895336 | ||||||
| chr3:57895345
|
C | A | 1 | a0001c0002t0001g0254 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1361-1166C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895345 | ||||||
| chr3:57895587
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-924G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895587 | ||||||
| chr3:57895680
|
G | T | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-831G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57895680 | ||||||
| chr3:57895943
|
C | CA | 39 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(36): Show | 39 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.1361-553dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57895943 | |||||
| chr3:57896010
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1361-501T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | chr3 | 57896010 | ||||||
| chr3:57896057
|
G | GT | 271 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1361-445dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 57896057 | |||||
| chr3:57896688
|
G | GA | 14 | a0001c0001t0002g0010a0001c0001t0002g0055a0001c0001t0002g0066others(11): Show | 14 | HG01175.hp1 HG02027.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1441+107dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr3 | 57896688 | |||||
| chr3:57896693
|
A | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+102A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 16/24 | chr3 | 57896693 | ||||||
| chr3:57896810
|
A | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1442-63A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 16/24 | chr3 | 57896810 | ||||||
| chr3:57897077
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0017others(17): Show | 20 | HG00544.hp1 HG00609.hp1 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.1501+145T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897077 | ||||||
| chr3:57897143
|
C | T | 4 | a0001c0001t0002g0069a0001c0002t0001g0221a0001c0002t0001g0274others(1): Show | 4 | HG02027.hp2 HG02735.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+211C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897143 | ||||||
| chr3:57897190
|
TTTGTTTA others(3): Show |
T | 1 | a0001c0001t0006g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1501+263_1501+272d others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57897190 | |||||
| chr3:57897207
|
C | T | 1 | a0001c0001t0015g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1501+275C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897207 | ||||||
| chr3:57897214
|
A | G | 1 | a0001c0002t0001g0215 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1501+282A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897214 | ||||||
| chr3:57897242
|
T | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+310T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897242 | ||||||
| chr3:57897406
|
T | C | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1501+474T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897406 | ||||||
| chr3:57897522
|
C | A | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+590C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897522 | ||||||
| chr3:57897539
|
G | A | 120 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(117): Show | 120 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1501+607G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897539 | ||||||
| chr3:57897552
|
C | T | 2 | a0001c0001t0003g0127a0001c0002t0001g0211 | 2 | HG00280.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1501+620C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897552 | ||||||
| chr3:57897566
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0034 | 2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1501+634C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897566 | ||||||
| chr3:57897589
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+657G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897589 | ||||||
| chr3:57897704
|
A | T | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01169.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+772A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897704 | ||||||
| chr3:57897706
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1501+774G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57897706 | ||||||
| chr3:57898106
|
T | C | 1 | a0001c0002t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1501+1174T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898106 | ||||||
| chr3:57898118
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1501+1186G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898118 | ||||||
| chr3:57898255
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1501+1323T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898255 | ||||||
| chr3:57898343
|
C | G | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1501+1411C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898343 | ||||||
| chr3:57898454
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1501+1522T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898454 | ||||||
| chr3:57898556
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1501+1624T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898556 | ||||||
| chr3:57898666
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1501+1734G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898666 | ||||||
| chr3:57898890
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1501+1958G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898890 | ||||||
| chr3:57898900
|
T | A | 1 | a0001c0002t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1501+1968T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898900 | ||||||
| chr3:57898959
|
T | C | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1501+2027T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57898959 | ||||||
| chr3:57899336
|
C | T | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1501+2404C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57899336 | ||||||
| chr3:57899341
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1501+2409G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57899341 | ||||||
| chr3:57899359
|
A | G | 35 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(32): Show | 35 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1501+2427A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57899359 | ||||||
| chr3:57899609
|
A | G | 2 | a0001c0002t0001g0221a0001c0002t0019g0220 | 2 | HG02735.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1501+2677A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57899609 | ||||||
| chr3:57899626
|
C | A | 1 | a0001c0001t0015g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1501+2694C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57899626 | ||||||
| chr3:57899978
|
T | TTTATG | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1501+3052_1501+305 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57899978 | |||||
| chr3:57900011
|
T | A | 1 | a0001c0001t0003g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1501+3079T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57900011 | ||||||
| chr3:57900199
|
T | A | 109 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1501+3267T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57900199 | ||||||
| chr3:57900540
|
A | C | 32 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.1501+3608A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57900540 | ||||||
| chr3:57900569
|
A | G | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+3637A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57900569 | ||||||
| chr3:57900736
|
G | A | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1501+3804G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57900736 | ||||||
| chr3:57901298
|
C | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0061 | 2 | NA18961.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1501+4366C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901298 | ||||||
| chr3:57901411
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1501+4479G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901411 | ||||||
| chr3:57901672
|
C | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1501+4740C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901672 | ||||||
| chr3:57901745
|
A | C | 3 | a0001c0001t0014g0082a0001c0001t0014g0098a0001c0001t0014g0102 | 3 | HG01257.hp2 HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1501+4813A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901745 | ||||||
| chr3:57901749
|
C | T | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+4817C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901749 | ||||||
| chr3:57901758
|
G | A | 6 | a0001c0001t0003g0182a0001c0001t0003g0192a0001c0001t0009g0116others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501+4826G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901758 | ||||||
| chr3:57901766
|
T | C | 1 | a0001c0001t0004g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1501+4834T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901766 | ||||||
| chr3:57901771
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501+4839C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901771 | ||||||
| chr3:57901813
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1501+4881C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901813 | ||||||
| chr3:57901904
|
A | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1501+4972A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901904 | ||||||
| chr3:57901957
|
C | T | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+5025C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57901957 | ||||||
| chr3:57902069
|
T | C | 124 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1501+5137T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902069 | ||||||
| chr3:57902180
|
G | C | 160 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1501+5248G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902180 | ||||||
| chr3:57902584
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1502-5300G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902584 | ||||||
| chr3:57902594
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1502-5290G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902594 | ||||||
| chr3:57902598
|
A | G | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.1502-5286A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902598 | ||||||
| chr3:57902641
|
T | G | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1502-5243T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902641 | ||||||
| chr3:57902652
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1502-5232T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902652 | ||||||
| chr3:57902861
|
T | C | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.1502-5023T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57902861 | ||||||
| chr3:57903184
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1502-4700G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903184 | ||||||
| chr3:57903385
|
G | C | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-4499G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903385 | ||||||
| chr3:57903407
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-4477A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903407 | ||||||
| chr3:57903428
|
T | A | 1 | a0001c0002t0001g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1502-4456T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903428 | ||||||
| chr3:57903515
|
G | C | 1 | a0001c0001t0034g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1502-4369G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903515 | ||||||
| chr3:57903518
|
T | A | 1 | a0001c0001t0001g0293 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1502-4366T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903518 | ||||||
| chr3:57903757
|
CA | C | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-4126delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57903757 | ||||||
| chr3:57904121
|
T | TAGTTATA others(4): Show |
4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3763_1502-376 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904121 | ||||||
| chr3:57904123
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3761G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904123 | ||||||
| chr3:57904125
|
A | C | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3759A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904125 | ||||||
| chr3:57904130
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3754G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904130 | ||||||
| chr3:57904131
|
T | TAATAACA | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3753_1502-375 others(11): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904131 | ||||||
| chr3:57904314
|
T | C | 1 | a0001c0001t0034g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1502-3570T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904314 | ||||||
| chr3:57904375
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3509C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904375 | ||||||
| chr3:57904377
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1502-3507T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904377 | ||||||
| chr3:57904388
|
C | T | 1 | a0001c0002t0001g0236 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1502-3496C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904388 | ||||||
| chr3:57904389
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-3495G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904389 | ||||||
| chr3:57904495
|
A | C | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1502-3389A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904495 | ||||||
| chr3:57904637
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0288others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1502-3247G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904637 | ||||||
| chr3:57904677
|
G | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0287others(8): Show | 11 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1502-3207G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904677 | ||||||
| chr3:57904699
|
C | T | 112 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1502-3185C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904699 | ||||||
| chr3:57904728
|
A | G | 1 | a0001c0001t0014g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1502-3156A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904728 | ||||||
| chr3:57904903
|
C | CA | 11 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0287others(8): Show | 11 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1502-2975dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57904903 | |||||
| chr3:57904907
|
A | C | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1502-2977A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904907 | ||||||
| chr3:57904971
|
G | T | 1 | a0001c0002t0002g0070 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1502-2913G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57904971 | ||||||
| chr3:57905036
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-2848A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905036 | ||||||
| chr3:57905110
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1502-2774A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905110 | ||||||
| chr3:57905178
|
C | CTGTGTGT others(3): Show |
8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-2705_1502-269 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57905178 | |||||
| chr3:57905248
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1502-2636G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905248 | ||||||
| chr3:57905261
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-2623A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905261 | ||||||
| chr3:57905313
|
ACTCTGTT others(1027): Show |
A | 1 | a0001c0002t0001g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1502-2564_1502-153 others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57905313 | |||||
| chr3:57905324
|
C | A | 1 | a0001c0001t0005g0166 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1502-2560C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905324 | ||||||
| chr3:57905330
|
G | A | 3 | a0001c0001t0012g0109a0001c0001t0012g0111a0001c0001t0012g0112 | 3 | HG02280.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1502-2554G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905330 | ||||||
| chr3:57905418
|
A | T | 1 | a0004c0010t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1502-2466A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905418 | ||||||
| chr3:57905462
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-2422A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905462 | ||||||
| chr3:57905471
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1502-2413G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905471 | ||||||
| chr3:57905551
|
T | G | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1502-2333T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905551 | ||||||
| chr3:57905602
|
C | A | 14 | a0001c0002t0001g0202a0001c0002t0001g0229a0001c0002t0001g0233others(11): Show | 14 | HG00673.hp2 HG02040.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.1502-2282C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905602 | ||||||
| chr3:57905657
|
A | G | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-2227A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905657 | ||||||
| chr3:57905782
|
T | C | 1 | a0001c0002t0002g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1502-2102T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905782 | ||||||
| chr3:57905789
|
A | G | 1 | a0001c0001t0016g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1502-2095A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57905789 | ||||||
| chr3:57906050
|
T | TA | 82 | a0001c0001t0001g0291a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1502-1813dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906050 | |||||
| chr3:57906050
|
TA | T | 22 | a0001c0001t0001g0292a0001c0001t0003g0008a0001c0001t0003g0009others(19): Show | 22 | HG00544.hp2 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1502-1813delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906050 | |||||
| chr3:57906106
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1502-1778A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906106 | ||||||
| chr3:57906295
|
T | C | 3 | a0001c0002t0001g0199a0001c0002t0001g0259a0001c0002t0001g0266 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1502-1589T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906295 | ||||||
| chr3:57906300
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(15): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(32): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0011g0179a0001c0001t0011g0191 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(23): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0011g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(27): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0011g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(34): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(32): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0037g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(36): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(35): Show |
1 | a0001c0001t0002g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(46): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0002g0309a0001c0002t0002g0015a0001c0002t0002g0070 | 3 | HG01516.hp1 NA18974.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(30): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(20): Show |
7 | a0001c0001t0002g0021a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG01106.hp1 NA18966.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(31): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(21): Show |
9 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0032others(6): Show | 9 | HG00438.hp1 HG00609.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(32): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(22): Show |
8 | a0001c0001t0002g0014a0001c0001t0002g0019a0001c0001t0002g0036others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(33): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0002g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(34): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(24): Show |
2 | a0001c0001t0002g0023a0001c0001t0002g0046 | 2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(35): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(25): Show |
5 | a0001c0001t0002g0024a0001c0001t0002g0038a0001c0001t0002g0066others(2): Show | 5 | NA18968.hp1 NA18977.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(36): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0002g0049a0001c0001t0002g0195 | 2 | HG01978.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(37): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(27): Show |
3 | a0001c0001t0002g0035a0001c0001t0002g0065a0001c0001t0002g0304 | 3 | HG02056.hp1 HG03239.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(38): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(28): Show |
2 | a0001c0001t0002g0022a0001c0001t0002g0052 | 2 | HG03669.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(39): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0002g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(40): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0002g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(41): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(32): Show |
2 | a0001c0001t0002g0029a0001c0001t0002g0053 | 2 | HG02083.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(43): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(34): Show |
1 | a0001c0001t0002g0061 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(45): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(35): Show |
1 | a0001c0001t0002g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(46): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(36): Show |
1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(47): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(20): Show |
1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(31): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0054 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1502-1575_1502-157 others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906300
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1502-1575_1502-157 others(27): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906300 | |||||
| chr3:57906304
|
T | C | 31 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(28): Show | 31 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1502-1580T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906304 | ||||||
| chr3:57906304
|
T | TTTTTC | 6 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0034others(3): Show | 6 | HG01928.hp2 HG01993.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-1576_1502-157 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906304 | |||||
| chr3:57906305
|
T | TTTTCTTT others(13): Show |
1 | a0001c0001t0002g0306 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1502-1576_1502-157 others(24): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906305 | |||||
| chr3:57906305
|
TTTTTC | T | 30 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(27): Show | 30 | HG01358.hp2 HG01361.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.1502-1574_1502-157 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906305 | |||||
| chr3:57906310
|
C | CT | 9 | a0001c0001t0002g0063a0001c0001t0003g0145a0001c0001t0003g0189others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1502-1552dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(1): Show |
16 | a0001c0001t0001g0142a0001c0001t0001g0289a0001c0001t0001g0293others(13): Show | 16 | HG00609.hp2 HG01074.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1502-1559_1502-155 others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1502-1566_1502-156 others(33): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0122a0001c0001t0001g0288a0001c0002t0001g0212others(10): Show | 13 | HG00438.hp2 HG00621.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1502-1560_1502-155 others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0217a0001c0002t0008g0243 | 2 | HG02080.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1502-1561_1502-155 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0295 | 3 | HG02258.hp2 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1502-1564_1502-155 others(17): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(9): Show |
2 | a0001c0002t0001g0202a0001c0002t0001g0262 | 2 | NA18991.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1502-1567_1502-155 others(20): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1502-1569_1502-155 others(22): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1502-1570_1502-155 others(23): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(15): Show |
1 | a0001c0002t0001g0221 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1502-1573_1502-155 others(26): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(16): Show |
7 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0256others(4): Show | 7 | HG01069.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(27): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(17): Show |
6 | a0001c0002t0001g0196a0001c0002t0001g0208a0001c0002t0001g0218others(3): Show | 6 | HG00639.hp2 HG01071.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(28): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(18): Show |
10 | a0001c0001t0001g0136a0001c0002t0001g0207a0001c0002t0001g0245others(7): Show | 10 | HG00673.hp2 HG02027.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(29): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(19): Show |
11 | a0001c0002t0001g0205a0001c0002t0001g0211a0001c0002t0001g0219others(8): Show | 11 | HG00735.hp2 HG01256.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(30): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(20): Show |
2 | a0001c0002t0001g0253a0001c0002t0001g0263 | 2 | HG00280.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(31): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(23): Show |
3 | a0001c0002t0001g0198a0001c0002t0001g0255a0001c0002t0001g0270 | 3 | HG00408.hp1 HG03669.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(34): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(24): Show |
4 | a0001c0002t0001g0199a0001c0002t0001g0233a0001c0002t0001g0259others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(35): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(25): Show |
3 | a0001c0002t0001g0236a0001c0002t0001g0244a0001c0002t0001g0248 | 3 | HG03834.hp2 NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(36): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(26): Show |
3 | a0001c0002t0001g0203a0001c0002t0001g0209a0001c0002t0001g0272 | 3 | HG00733.hp1 HG03688.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1502-1552_1502-155 others(37): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(28): Show |
1 | a0001c0002t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1502-1552_1502-155 others(39): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(30): Show |
1 | a0001c0002t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1502-1552_1502-155 others(41): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | CTTTTTTT others(35): Show |
1 | a0001c0002t0001g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1502-1552_1502-155 others(46): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906310 | |||||
| chr3:57906310
|
C | T | 77 | a0001c0001t0001g0119a0001c0001t0001g0291a0001c0001t0002g0011others(74): Show | 77 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1502-1574C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906310 | ||||||
| chr3:57906311
|
T | C | 4 | a0001c0001t0002g0030a0001c0001t0002g0068a0001c0001t0018g0002others(1): Show | 4 | NA18939.hp1 NA18941.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-1573T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906311 | ||||||
| chr3:57906312
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0050a0001c0001t0038g0047others(1): Show | 4 | HG02300.hp2 NA18948.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1502-1572T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906312 | ||||||
| chr3:57906313
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1502-1571T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906313 | ||||||
| chr3:57906316
|
T | C | 3 | a0001c0001t0002g0059a0001c0001t0003g0008a0001c0001t0003g0009 | 3 | HG02559.hp1 HG03453.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1502-1568T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906316 | ||||||
| chr3:57906317
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1502-1567T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906317 | ||||||
| chr3:57906317
|
T | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-1567T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906317 | ||||||
| chr3:57906325
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1502-1559T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906325 | ||||||
| chr3:57906332
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1502-1552T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906332 | ||||||
| chr3:57906332
|
T | TTTTTTTT others(9): Show |
1 | a0001c0001t0002g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1502-1552_1502-155 others(20): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906332 | ||||||
| chr3:57906334
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1502-1550G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906334 | ||||||
| chr3:57906378
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1502-1506C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906378 | ||||||
| chr3:57906379
|
G | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-1505G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906379 | ||||||
| chr3:57906420
|
A | G | 32 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.1502-1464A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906420 | ||||||
| chr3:57906438
|
C | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-1446C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906438 | ||||||
| chr3:57906515
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-1369A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906515 | ||||||
| chr3:57906531
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-1353G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906531 | ||||||
| chr3:57906607
|
G | A | 7 | a0001c0001t0006g0074a0001c0001t0006g0096a0001c0001t0006g0100others(4): Show | 7 | HG00544.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-1277G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906607 | ||||||
| chr3:57906666
|
GAA | G | 7 | a0001c0001t0003g0144a0001c0001t0003g0168a0001c0001t0003g0169others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-1210_1502-120 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906666 | |||||
| chr3:57906672
|
A | T | 1 | a0001c0001t0003g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1502-1212A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906672 | ||||||
| chr3:57906673
|
AAATAT | A | 6 | a0001c0001t0004g0075a0001c0001t0004g0081a0001c0001t0004g0108others(3): Show | 6 | HG01255.hp2 HG01361.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1502-1209_1502-120 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906673 | |||||
| chr3:57906673
|
AAATATAT others(2): Show |
A | 7 | a0001c0001t0003g0009a0001c0001t0010g0300a0001c0001t0010g0301others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-1209_1502-120 others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906673 | |||||
| chr3:57906674
|
A | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0128 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1502-1210A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906674 | ||||||
| chr3:57906674
|
AAT | A | 9 | a0001c0001t0003g0140a0001c0001t0003g0167a0001c0001t0003g0171others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1502-1184_1502-118 others(6): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906674 | |||||
| chr3:57906674
|
AATATAT | A | 115 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1502-1188_1502-118 others(10): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906674 | |||||
| chr3:57906674
|
AATATATA others(1): Show |
A | 75 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(72): Show | 75 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1502-1190_1502-118 others(12): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906674 | |||||
| chr3:57906674
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1502-1192_1502-118 others(14): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57906674 | |||||
| chr3:57906675
|
AT | A | 5 | a0001c0001t0003g0308a0001c0001t0005g0135a0001c0001t0005g0152others(2): Show | 5 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1502-1208delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906675 | ||||||
| chr3:57906675
|
ATAT | A | 28 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(25): Show | 28 | HG00639.hp1 HG00733.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1502-1208_1502-120 others(7): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906675 | ||||||
| chr3:57906675
|
ATATAT | A | 21 | a0001c0001t0001g0136a0001c0001t0004g0080a0001c0001t0004g0084others(18): Show | 21 | HG01175.hp1 HG01358.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1502-1208_1502-120 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906675 | ||||||
| chr3:57906675
|
ATATATAT | A | 5 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-1208_1502-120 others(11): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906675 | ||||||
| chr3:57906675
|
ATATATAT others(2): Show |
A | 3 | a0001c0001t0003g0008a0001c0001t0004g0095a0001c0001t0033g0305 | 3 | HG02559.hp1 HG03209.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1502-1208_1502-120 others(13): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906675 | ||||||
| chr3:57906676
|
T | A | 5 | a0001c0001t0003g0126a0001c0001t0003g0129a0001c0001t0006g0074others(2): Show | 5 | HG00544.hp2 HG01993.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1502-1208T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906676 | ||||||
| chr3:57906678
|
T | A | 7 | a0001c0001t0003g0307a0001c0001t0005g0152a0001c0001t0005g0183others(4): Show | 7 | HG00099.hp1 HG01069.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-1206T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906678 | ||||||
| chr3:57906680
|
T | A | 31 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(28): Show | 31 | HG00639.hp1 HG00733.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1502-1204T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906680 | ||||||
| chr3:57906682
|
T | A | 64 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0287others(61): Show | 64 | HG00621.hp2 HG00639.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1502-1202T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906682 | ||||||
| chr3:57906684
|
T | A | 89 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0287others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1502-1200T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906684 | ||||||
| chr3:57906686
|
T | A | 14 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0291others(11): Show | 14 | HG01099.hp2 HG01934.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1502-1198T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906686 | ||||||
| chr3:57906719
|
T | C | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1502-1165T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906719 | ||||||
| chr3:57906903
|
A | G | 5 | a0001c0002t0001g0196a0001c0002t0001g0199a0001c0002t0001g0237others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1502-981A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57906903 | ||||||
| chr3:57907028
|
G | GT | 9 | a0001c0001t0002g0286a0001c0001t0004g0075a0001c0001t0011g0181others(6): Show | 9 | HG01099.hp2 HG02145.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1502-845dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 57907028 | |||||
| chr3:57907055
|
T | A | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1502-829T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907055 | ||||||
| chr3:57907097
|
G | A | 5 | a0001c0002t0001g0214a0001c0002t0001g0222a0001c0002t0001g0241others(2): Show | 5 | HG01978.hp2 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-787G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907097 | ||||||
| chr3:57907265
|
G | T | 1 | a0001c0002t0029g0280 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1502-619G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907265 | ||||||
| chr3:57907322
|
C | T | 4 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | HG01169.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-562C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907322 | ||||||
| chr3:57907323
|
A | G | 235 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(232): Show | 235 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1502-561A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907323 | ||||||
| chr3:57907565
|
C | G | 11 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1502-319C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907565 | ||||||
| chr3:57907626
|
G | A | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1502-258G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907626 | ||||||
| chr3:57907780
|
A | G | 115 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1502-104A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 17/24 | chr3 | 57907780 | ||||||
| chr3:57908046
|
A | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1624+40A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908046 | ||||||
| chr3:57908086
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1624+80C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908086 | ||||||
| chr3:57908091
|
G | T | 1 | a0001c0001t0004g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1624+85G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908091 | ||||||
| chr3:57908200
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1624+194A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908200 | ||||||
| chr3:57908288
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1624+282G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908288 | ||||||
| chr3:57908316
|
T | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1624+310T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908316 | ||||||
| chr3:57908346
|
T | C | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1624+340T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908346 | ||||||
| chr3:57908426
|
C | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1624+420C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908426 | ||||||
| chr3:57908443
|
T | C | 1 | a0001c0001t0015g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1624+437T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908443 | ||||||
| chr3:57908496
|
T | C | 115 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1624+490T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908496 | ||||||
| chr3:57908556
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1625-520A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908556 | ||||||
| chr3:57908679
|
G | A | 1 | a0001c0001t0009g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1625-397G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908679 | ||||||
| chr3:57908971
|
A | G | 1 | a0001c0001t0034g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1625-105A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 18/24 | chr3 | 57908971 | ||||||
| chr3:57909180
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1699+30T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909180 | ||||||
| chr3:57909195
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1699+45G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909195 | ||||||
| chr3:57909238
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1699+88C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909238 | ||||||
| chr3:57909317
|
C | A | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1699+167C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909317 | ||||||
| chr3:57909443
|
A | G | 1 | a0001c0001t0002g0019 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1699+293A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909443 | ||||||
| chr3:57909503
|
G | GA | 77 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(74): Show | 77 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1699+368dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57909503 | |||||
| chr3:57909503
|
G | GAA | 49 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(46): Show | 49 | HG01099.hp2 HG01175.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.1699+367_1699+368d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57909503 | |||||
| chr3:57909566
|
G | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1699+416G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909566 | ||||||
| chr3:57909681
|
C | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1699+531C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909681 | ||||||
| chr3:57909770
|
A | G | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1699+620A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909770 | ||||||
| chr3:57909913
|
A | AT | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0094others(8): Show | 11 | HG01099.hp2 HG01358.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1699+779dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57909913 | |||||
| chr3:57909913
|
AT | A | 146 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(143): Show | 146 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1699+779delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57909913 | |||||
| chr3:57909942
|
A | T | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1699+792A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57909942 | ||||||
| chr3:57910252
|
T | C | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1699+1102T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910252 | ||||||
| chr3:57910282
|
C | T | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1699+1132C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910282 | ||||||
| chr3:57910327
|
G | A | 32 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.1699+1177G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910327 | ||||||
| chr3:57910381
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1699+1231A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910381 | ||||||
| chr3:57910593
|
A | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1699+1443A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910593 | ||||||
| chr3:57910597
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1699+1447G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910597 | ||||||
| chr3:57910645
|
T | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1699+1495T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910645 | ||||||
| chr3:57910743
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1699+1593A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57910743 | ||||||
| chr3:57911374
|
G | C | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1700-1007G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911374 | ||||||
| chr3:57911722
|
A | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1700-659A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911722 | ||||||
| chr3:57911741
|
A | C | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1700-640A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911741 | ||||||
| chr3:57911812
|
G | A | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1700-569G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911812 | ||||||
| chr3:57911855
|
G | A | 32 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0189others(29): Show | 32 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1700-526G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911855 | ||||||
| chr3:57911923
|
T | TA | 16 | a0001c0001t0003g0008a0001c0001t0003g0129a0001c0001t0003g0145others(13): Show | 16 | HG01109.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1700-432dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57911923 | |||||
| chr3:57911923
|
TA | T | 156 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0136others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1700-432delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57911923 | |||||
| chr3:57911923
|
TAA | T | 10 | a0001c0001t0002g0029a0001c0001t0002g0033a0001c0001t0003g0182others(7): Show | 10 | HG01099.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1700-433_1700-432d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr3 | 57911923 | |||||
| chr3:57911995
|
A | C | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0266 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1700-386A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57911995 | ||||||
| chr3:57912084
|
T | A | 307 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1700-297T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57912084 | ||||||
| chr3:57912113
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1700-268G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57912113 | ||||||
| chr3:57912152
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1700-229A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57912152 | ||||||
| chr3:57912158
|
A | G | 49 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0075others(46): Show | 49 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1700-223A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57912158 | ||||||
| chr3:57912203
|
G | A | 1 | a0001c0002t0008g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1700-178G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 19/24 | chr3 | 57912203 | ||||||
| chr3:57912771
|
G | A | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(8): Show | 11 | HG01934.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2020+70G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 20/24 | chr3 | 57912771 | ||||||
| chr3:57912890
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2020+189C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 20/24 | chr3 | 57912890 | ||||||
| chr3:57912984
|
A | C | 1 | a0001c0002t0001g0208 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2021-174A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 20/24 | chr3 | 57912984 | ||||||
| chr3:57913450
|
T | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2138+175T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57913450 | ||||||
| chr3:57913539
|
A | C | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2138+264A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57913539 | ||||||
| chr3:57913601
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2138+326G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57913601 | ||||||
| chr3:57913639
|
C | T | 30 | a0001c0001t0003g0141a0001c0001t0005g0135a0001c0001t0005g0137others(27): Show | 30 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.2138+364C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57913639 | ||||||
| chr3:57913859
|
G | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0030others(6): Show | 9 | NA18939.hp1 NA18941.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2138+584G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57913859 | ||||||
| chr3:57914067
|
C | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2138+792C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914067 | ||||||
| chr3:57914321
|
G | T | 2 | a0001c0001t0009g0116a0001c0001t0009g0117 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2138+1046G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914321 | ||||||
| chr3:57914522
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2138+1247G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914522 | ||||||
| chr3:57914768
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2138+1493G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914768 | ||||||
| chr3:57914770
|
C | T | 5 | a0001c0002t0001g0196a0001c0002t0001g0199a0001c0002t0001g0237others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2138+1495C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914770 | ||||||
| chr3:57914811
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2138+1536A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57914811 | ||||||
| chr3:57914886
|
A | AT | 41 | a0001c0001t0002g0036a0001c0001t0002g0286a0001c0001t0004g0075others(38): Show | 41 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2138+1628dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 57914886 | |||||
| chr3:57914886
|
AT | A | 10 | a0001c0001t0002g0061a0001c0001t0003g0008a0001c0001t0003g0009others(7): Show | 10 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2138+1628delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 57914886 | |||||
| chr3:57915148
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2139-1758G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915148 | ||||||
| chr3:57915237
|
C | A | 2 | a0001c0001t0011g0180a0001c0001t0011g0181 | 2 | HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2139-1669C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915237 | ||||||
| chr3:57915460
|
T | C | 1 | a0001c0002t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2139-1446T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915460 | ||||||
| chr3:57915461
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2139-1445C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915461 | ||||||
| chr3:57915549
|
A | C | 1 | a0001c0002t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2139-1357A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915549 | ||||||
| chr3:57915620
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2139-1286A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915620 | ||||||
| chr3:57915753
|
T | C | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2139-1153T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915753 | ||||||
| chr3:57915760
|
G | A | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2139-1146G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915760 | ||||||
| chr3:57915802
|
C | T | 1 | a0001c0001t0004g0106 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2139-1104C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915802 | ||||||
| chr3:57915856
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2139-1050C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915856 | ||||||
| chr3:57915905
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2139-1001C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915905 | ||||||
| chr3:57915927
|
C | G | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2139-979C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915927 | ||||||
| chr3:57915973
|
G | A | 120 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(117): Show | 120 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.2139-933G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57915973 | ||||||
| chr3:57916025
|
G | A | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2139-881G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57916025 | ||||||
| chr3:57916156
|
C | CA | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2139-736dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 57916156 | |||||
| chr3:57916705
|
G | A | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2139-201G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57916705 | ||||||
| chr3:57916726
|
T | A | 1 | a0001c0001t0027g0246 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2139-180T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57916726 | ||||||
| chr3:57916871
|
C | T | 2 | a0001c0002t0002g0015a0001c0002t0002g0056 | 2 | NA18974.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2139-35C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 21/24 | chr3 | 57916871 | ||||||
| chr3:57917195
|
T | C | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2310+118T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917195 | ||||||
| chr3:57917374
|
C | T | 2 | a0001c0002t0001g0269a0001c0002t0001g0284 | 2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2310+297C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917374 | ||||||
| chr3:57917390
|
C | T | 3 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0295 | 3 | HG02258.hp2 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2310+313C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917390 | ||||||
| chr3:57917418
|
G | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2310+341G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917418 | ||||||
| chr3:57917434
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2310+357C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917434 | ||||||
| chr3:57917686
|
G | A | 236 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(233): Show | 236 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.2310+609G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917686 | ||||||
| chr3:57917779
|
A | C | 1 | a0001c0001t0002g0066 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2310+702A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917779 | ||||||
| chr3:57917845
|
C | T | 4 | a0001c0001t0009g0116a0001c0001t0009g0117a0001c0001t0009g0118others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2310+768C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917845 | ||||||
| chr3:57917948
|
A | G | 1 | a0001c0002t0008g0277 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2310+871A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57917948 | ||||||
| chr3:57918094
|
C | T | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2310+1017C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918094 | ||||||
| chr3:57918115
|
G | T | 1 | a0001c0001t0002g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2310+1038G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918115 | ||||||
| chr3:57918322
|
G | A | 4 | a0001c0001t0012g0109a0001c0001t0012g0110a0001c0001t0012g0111others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+1245G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918322 | ||||||
| chr3:57918438
|
T | A | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2310+1361T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918438 | ||||||
| chr3:57918585
|
C | G | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2310+1508C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918585 | ||||||
| chr3:57918726
|
G | A | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0010g0300others(10): Show | 13 | HG01934.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2310+1649G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57918726 | ||||||
| chr3:57919122
|
T | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2310+2045T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919122 | ||||||
| chr3:57919153
|
G | T | 1 | a0001c0002t0001g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2310+2076G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919153 | ||||||
| chr3:57919296
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2310+2219G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919296 | ||||||
| chr3:57919567
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2310+2490A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919567 | ||||||
| chr3:57919577
|
C | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2310+2500C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919577 | ||||||
| chr3:57919744
|
A | G | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2310+2667A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919744 | ||||||
| chr3:57919795
|
C | CA | 6 | a0001c0001t0003g0125a0001c0001t0003g0182a0001c0001t0006g0103others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+2734dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57919795 | |||||
| chr3:57919795
|
CA | C | 6 | a0001c0001t0002g0028a0001c0001t0003g0138a0001c0001t0005g0152others(3): Show | 6 | HG01069.hp2 HG01099.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+2734delA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57919795 | |||||
| chr3:57919980
|
C | A | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2310+2903C>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57919980 | ||||||
| chr3:57920040
|
G | C | 1 | a0001c0002t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2311-2849G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920040 | ||||||
| chr3:57920114
|
G | C | 2 | a0001c0002t0001g0218a0001c0002t0021g0239 | 2 | NA18977.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2311-2775G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920114 | ||||||
| chr3:57920377
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2311-2512A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920377 | ||||||
| chr3:57920417
|
C | T | 1 | a0001c0001t0006g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2311-2472C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920417 | ||||||
| chr3:57920600
|
A | C | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2311-2289A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920600 | ||||||
| chr3:57920697
|
A | G | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2311-2192A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920697 | ||||||
| chr3:57920808
|
A | G | 88 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0201others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2311-2081A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920808 | ||||||
| chr3:57920973
|
C | T | 2 | a0001c0001t0025g0003a0001c0001t0032g0004 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2311-1916C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57920973 | ||||||
| chr3:57921043
|
G | A | 1 | a0001c0002t0019g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2311-1846G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921043 | ||||||
| chr3:57921105
|
T | C | 1 | a0001c0001t0032g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2311-1784T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921105 | ||||||
| chr3:57921161
|
C | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2311-1728C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921161 | ||||||
| chr3:57921214
|
G | T | 32 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2311-1675G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921214 | ||||||
| chr3:57921281
|
A | T | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2311-1608A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921281 | ||||||
| chr3:57921420
|
A | G | 2 | a0001c0002t0001g0218a0001c0002t0021g0239 | 2 | NA18977.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2311-1469A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921420 | ||||||
| chr3:57921446
|
G | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-1443G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921446 | ||||||
| chr3:57921621
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2311-1268G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921621 | ||||||
| chr3:57921656
|
T | C | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0004t0002g0013others(1): Show | 4 | HG01106.hp1 HG01516.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-1233T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921656 | ||||||
| chr3:57921784
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-1105C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921784 | ||||||
| chr3:57921820
|
C | T | 23 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0229others(20): Show | 23 | HG00673.hp2 HG01928.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.2311-1069C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921820 | ||||||
| chr3:57921821
|
G | A | 1 | a0001c0001t0033g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2311-1068G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57921821 | ||||||
| chr3:57922052
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2311-837C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922052 | ||||||
| chr3:57922108
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2311-781A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922108 | ||||||
| chr3:57922237
|
A | G | 1 | a0001c0001t0003g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2311-652A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922237 | ||||||
| chr3:57922385
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-504A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922385 | ||||||
| chr3:57922395
|
C | T | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-494C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922395 | ||||||
| chr3:57922416
|
A | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-473A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922416 | ||||||
| chr3:57922425
|
C | CT | 12 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(9): Show | 12 | HG00280.hp1 HG00673.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.2311-445dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57922425 | |||||
| chr3:57922425
|
C | CTT | 10 | a0001c0001t0005g0194a0001c0001t0010g0300a0001c0001t0010g0301others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2311-446_2311-445d others(4): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57922425 | |||||
| chr3:57922425
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0127 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2311-464C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922425 | ||||||
| chr3:57922425
|
CT | C | 72 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(69): Show | 72 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2311-445delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57922425 | |||||
| chr3:57922484
|
A | T | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2311-405A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922484 | ||||||
| chr3:57922522
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2311-367G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922522 | ||||||
| chr3:57922693
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-196C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922693 | ||||||
| chr3:57922742
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0023a0001c0001t0002g0039others(2): Show | 5 | HG00438.hp1 HG00621.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2311-147A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | chr3 | 57922742 | ||||||
| chr3:57922867
|
CT | C | 71 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2311-13delT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 57922867 | |||||
| chr3:57923284
|
T | C | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2445+261T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923284 | ||||||
| chr3:57923327
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2445+304A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923327 | ||||||
| chr3:57923367
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2445+344A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923367 | ||||||
| chr3:57923372
|
A | C | 36 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(33): Show | 36 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.2445+349A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923372 | ||||||
| chr3:57923531
|
T | G | 35 | a0001c0001t0004g0075a0001c0001t0004g0080a0001c0001t0004g0081others(32): Show | 35 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.2445+508T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923531 | ||||||
| chr3:57923647
|
G | A | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2445+624G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923647 | ||||||
| chr3:57923749
|
A | T | 32 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0080others(29): Show | 32 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2445+726A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57923749 | ||||||
| chr3:57924035
|
ATGGTT | A | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445+1018_2445+102 others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr3 | 57924035 | |||||
| chr3:57924094
|
C | G | 1 | a0001c0002t0002g0051 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2445+1071C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924094 | ||||||
| chr3:57924424
|
A | C | 2 | a0001c0002t0001g0217a0001c0002t0024g0216 | 2 | HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2445+1401A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924424 | ||||||
| chr3:57924454
|
C | T | 7 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(4): Show | 7 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2446-1391C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924454 | ||||||
| chr3:57924458
|
T | A | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1387T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924458 | ||||||
| chr3:57924460
|
C | G | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1385C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924460 | ||||||
| chr3:57924463
|
G | C | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1382G>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924463 | ||||||
| chr3:57924464
|
G | T | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1381G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924464 | ||||||
| chr3:57924465
|
T | A | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1380T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924465 | ||||||
| chr3:57924468
|
A | T | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1377A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924468 | ||||||
| chr3:57924469
|
A | C | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1376A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924469 | ||||||
| chr3:57924470
|
G | A | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1375G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924470 | ||||||
| chr3:57924471
|
C | G | 1 | a0001c0001t0036g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2446-1374C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924471 | ||||||
| chr3:57924473
|
G | A | 46 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0004g0075others(43): Show | 46 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.2446-1372G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924473 | ||||||
| chr3:57924674
|
T | C | 1 | a0001c0002t0001g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2446-1171T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924674 | ||||||
| chr3:57924828
|
A | G | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2446-1017A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924828 | ||||||
| chr3:57924904
|
A | C | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2446-941A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924904 | ||||||
| chr3:57924934
|
G | GTGTTTTT | 29 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0081others(26): Show | 29 | HG01175.hp1 HG01257.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.2446-888_2446-882d others(9): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr3 | 57924934 | |||||
| chr3:57924943
|
G | T | 3 | a0001c0002t0001g0249a0001c0002t0001g0252a0001c0002t0001g0283 | 3 | HG00673.hp2 HG02040.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2446-902G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924943 | ||||||
| chr3:57924957
|
G | GT | 20 | a0001c0001t0002g0011a0001c0001t0002g0020a0001c0001t0002g0039others(17): Show | 20 | HG00438.hp1 HG01109.hp2 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.2446-874dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr3 | 57924957 | |||||
| chr3:57924957
|
G | T | 1 | a0001c0001t0006g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2446-888G>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924957 | ||||||
| chr3:57924964
|
T | G | 2 | a0001c0001t0003g0008a0001c0002t0001g0196 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2446-881T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924964 | ||||||
| chr3:57924966
|
T | G | 1 | a0001c0009t0031g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2446-879T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57924966 | ||||||
| chr3:57925000
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0142a0001c0001t0001g0288others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446-845G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925000 | ||||||
| chr3:57925116
|
A | T | 1 | a0001c0001t0014g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2446-729A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925116 | ||||||
| chr3:57925259
|
C | T | 4 | a0001c0001t0011g0179a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01099.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2446-586C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925259 | ||||||
| chr3:57925296
|
A | C | 1 | a0001c0001t0005g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2446-549A>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925296 | ||||||
| chr3:57925334
|
C | CT | 73 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2446-496dupT | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr3 | 57925334 | |||||
| chr3:57925335
|
T | TC | 113 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2446-510_2446-509i others(3): Show |
SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925335 | ||||||
| chr3:57925337
|
T | C | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2446-508T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925337 | ||||||
| chr3:57925344
|
T | G | 1 | a0001c0001t0005g0152 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2446-501T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925344 | ||||||
| chr3:57925354
|
G | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0192 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2446-491G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925354 | ||||||
| chr3:57925487
|
C | G | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2446-358C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 23/24 | chr3 | 57925487 | ||||||
| chr3:57926385
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*6+451C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926385 | ||||||
| chr3:57926391
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0068 | 2 | NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.*6+457C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926391 | ||||||
| chr3:57926523
|
C | T | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.*6+589C>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926523 | ||||||
| chr3:57926668
|
A | T | 6 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0051others(3): Show | 6 | NA18974.hp2 NA18984.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7-628A>T | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926668 | ||||||
| chr3:57926743
|
T | C | 1 | a0001c0001t0025g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*7-553T>C | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926743 | ||||||
| chr3:57926821
|
G | A | 8 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.*7-475G>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926821 | ||||||
| chr3:57926945
|
A | G | 3 | a0001c0001t0016g0005a0001c0001t0016g0006a0001c0001t0016g0007 | 3 | HG01934.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.*7-351A>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57926945 | ||||||
| chr3:57927100
|
T | G | 9 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(6): Show | 9 | HG01934.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.*7-196T>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57927100 | ||||||
| chr3:57927138
|
C | CA | 94 | a0001c0001t0001g0136a0001c0002t0001g0196a0001c0002t0001g0197others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.*7-157dupA | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr3 | 57927138 | |||||
| chr3:57927182
|
T | A | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*7-114T>A | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57927182 | ||||||
| chr3:57927200
|
C | G | 4 | a0001c0001t0010g0300a0001c0001t0010g0301a0001c0001t0010g0302others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.*7-96C>G | SLMAP | ENSG00000163681.17 | transcript | ENST00000671191.1 | protein_coding | 24/24 | chr3 | 57927200 |