Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51684 |
|---|---|
| ensemblid | ENSG00000107882.12 |
| hgncid | 16466 |
| symbol | SUFU |
| name | SUFU negative regulator of hedgehog signaling |
| refseq_nuc | NM_016169.4 |
| refseq_prot | NP_057253.2 |
| ensembl_nuc | ENST00000369902.8 |
| ensembl_prot | ENSP00000358918.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 102503972 |
| end | 102633535 |
| strand | + |
| ver | v1.2 |
| region | chr10:102503972-102633535 |
| region5000 | chr10:102498972-102638535 |
| regionname0 | SUFU_chr10_102503972_102633535 |
| regionname5000 | SUFU_chr10_102498972_102638535 |
| 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 | 484 | 268 | 60 | 56 | 106 | 8 | 36 | 84 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| 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 | 1455 | 189 | 45 | 47 | 62 | 6 | 27 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| c0002 | 0/0 | 1455 | 76 | 15 | 9 | 42 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| c0003 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| c0004 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| c0005 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| 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 | 0/1 | 3562 | 92 | 14 | 24 | 32 | 4 | 17 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0002 | 0/0 | 3562 | 64 | 7 | 8 | 39 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0003 | 0/0 | 3562 | 26 | 6 | 9 | 5 | 2 | 4 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0004 | 0/0 | 3562 | 21 | 0 | 5 | 16 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0005 | 0/0 | 3562 | 13 | 11 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0006 | 0/0 | 3562 | 12 | 0 | 0 | 8 | 0 | 4 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0007 | 0/0 | 3562 | 5 | 5 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0008 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0009 | 0/0 | 3562 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0010 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0011 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0012 | 0/0 | 3562 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0013 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0014 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0015 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0016 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0017 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0018 | 0/0 | 3562 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0019 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0020 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0021 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0022 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0023 | 0/0 | 3562 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0024 | 0/0 | 3562 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0025 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0026 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0027 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0028 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0029 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0030 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0031 | 0/0 | 3562 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0032 | 1/0 | 3562 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0033 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0034 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| t0035 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| 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 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| 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 | 1455 | 189 | 45 | 47 | 62 | 6 | 27 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002 | 0/0 | 1455 | 76 | 15 | 9 | 42 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0003 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0004 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0005 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5016 | 92 | 14 | 24 | 32 | 4 | 17 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0003 | 0/0 | 5016 | 24 | 6 | 9 | 4 | 2 | 3 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0004 | 0/0 | 5016 | 20 | 0 | 5 | 15 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0005 | 0/0 | 5016 | 13 | 11 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0006 | 0/0 | 5016 | 12 | 0 | 0 | 8 | 0 | 4 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0008 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0009 | 0/0 | 5016 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0010 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0011 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0012 | 0/0 | 5016 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0013 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0014 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0015 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0016 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0017 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0018 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0019 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0020 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0021 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0022 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0023 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0024 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0031 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0032 | 1/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0033 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0001t0034 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0002 | 0/0 | 5016 | 64 | 7 | 8 | 39 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0007 | 0/0 | 5016 | 5 | 5 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0025 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0026 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0027 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0028 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0029 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0030 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0002t0035 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0003t0003 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0004t0003 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| a0001c0005t0004 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | copy fasta | chr10 | 102498972 | 102638535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0012g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0012g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0015g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0016g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0017g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0019g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0021g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0022g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0023g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0024g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0031g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0032g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0033g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0034g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0025g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0027g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0028g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0029g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0030g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0035g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0005t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | FIN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00558 | hp1 | a0001 | c0001 | t0019 | g0205 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00597 | hp1 | a0001 | c0003 | t0003 | g0220 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0236 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0192 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0080 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01175 | hp1 | a0001 | c0001 | t0012 | g0262 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01346 | hp2 | a0001 | c0001 | t0021 | g0153 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01433 | hp1 | a0001 | c0001 | t0022 | g0233 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | IBS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0265 | EUR | IBS | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01943 | hp2 | a0001 | c0002 | t0030 | g0089 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01952 | hp1 | a0001 | c0001 | t0017 | g0200 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | CDX | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0189 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02451 | hp2 | a0001 | c0002 | t0007 | g0105 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0249 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02615 | hp2 | a0001 | c0002 | t0026 | g0036 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02622 | hp2 | a0001 | c0002 | t0029 | g0037 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02683 | hp2 | a0001 | c0001 | t0018 | g0241 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0052 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0248 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0231 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02922 | hp2 | a0001 | c0002 | t0035 | g0084 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0017 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0103 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0106 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0099 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0261 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0216 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0104 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03654 | hp1 | a0001 | c0001 | t0024 | g0252 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0263 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0038 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0226 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0041 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG04228 | hp2 | a0001 | c0001 | t0023 | g0180 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0092 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18906 | hp2 | a0001 | c0002 | t0007 | g0160 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18952 | hp2 | a0001 | c0001 | t0031 | g0258 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18954 | hp1 | a0001 | c0005 | t0004 | g0165 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18960 | hp2 | a0001 | c0001 | t0016 | g0191 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18975 | hp1 | a0001 | c0002 | t0028 | g0086 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18981 | hp1 | a0001 | c0002 | t0025 | g0065 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19004 | hp1 | a0001 | c0002 | t0027 | g0056 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | LWK | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | LWK | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19043 | hp1 | a0001 | c0001 | t0034 | g0076 | AFR | LWK | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0122 | AFR | LWK | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0137 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | YRI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0014 | EUR | TSI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0013 | EUR | TSI | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0268 | SAS | GIH | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02486 | hp2 | a0001 | c0001 | t0033 | g0069 | AFR | ACB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0085 | AFR | USA | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0203 | REF | REF | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0032 | g0068 | REF | REF | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102550093
|
C | T | 1 | a0001c0005 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.441C>T | p.Tyr147Tyr | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/12 | 622/5016 | 441/1455 | 147/484 | chr10 | 102550093 | ||
| chr10:102593683
|
C | T | 1 | a0001c0004 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.645C>T | p.Asn215Asn | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 5/12 | 826/5016 | 645/1455 | 215/484 | chr10 | 102593683 | ||
| chr10:102597238
|
C | T | 1 | a0001c0003 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.855C>T | p.Asp285Asp | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/12 | 1036/5016 | 855/1455 | 285/484 | chr10 | 102597238 | ||
| chr10:102627177
|
T | C | 1 | a0001c0002 | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
splice_region_variant&synonymous_variant | LOW | c.1299T>C | p.Ile433Ile | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/12 | 1480/5016 | 1299/1455 | 433/484 | chr10 | 102627177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102503975
|
C | T | 3 | a0001c0001t0005a0001c0001t0034a0001c0002t0035 | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-178C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/12 | 178 | chr10 | 102503975 | |||||
| chr10:102504120
|
C | T | 2 | a0001c0001t0014a0001c0001t0033 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-33C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/12 | 33 | chr10 | 102504120 | |||||
| chr10:102630175
|
T | G | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*20T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 20 | chr10 | 102630175 | |||||
| chr10:102630273
|
C | T | 2 | a0001c0001t0004a0001c0005t0004 | 21 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*118C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 118 | chr10 | 102630273 | |||||
| chr10:102630360
|
G | A | 1 | a0001c0001t0008 | 2 | HG03225.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*205G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 205 | chr10 | 102630360 | |||||
| chr10:102630498
|
C | T | 1 | a0001c0001t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 343 | chr10 | 102630498 | |||||
| chr10:102630546
|
A | G | 9 | a0001c0002t0002a0001c0002t0007a0001c0002t0025others(6): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*391A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 391 | chr10 | 102630546 | |||||
| chr10:102630562
|
T | G | 1 | a0001c0001t0015 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*407T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 407 | chr10 | 102630562 | |||||
| chr10:102630660
|
T | G | 1 | a0001c0002t0035 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*505T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 505 | chr10 | 102630660 | |||||
| chr10:102631016
|
G | C | 1 | a0001c0001t0016 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*861G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 861 | chr10 | 102631016 | |||||
| chr10:102631277
|
C | T | 11 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(8): Show | 47 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1122 | chr10 | 102631277 | |||||
| chr10:102631415
|
T | A | 1 | a0001c0002t0025 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1260T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1260 | chr10 | 102631415 | |||||
| chr10:102631528
|
C | T | 9 | a0001c0002t0002a0001c0002t0007a0001c0002t0025others(6): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1373C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1373 | chr10 | 102631528 | |||||
| chr10:102631533
|
C | A | 1 | a0001c0001t0022 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1378C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1378 | chr10 | 102631533 | |||||
| chr10:102631769
|
C | G | 1 | a0001c0001t0024 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1614C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1614 | chr10 | 102631769 | |||||
| chr10:102631788
|
C | T | 9 | a0001c0002t0002a0001c0002t0007a0001c0002t0025others(6): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1633C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1633 | chr10 | 102631788 | |||||
| chr10:102631827
|
A | G | 1 | a0001c0001t0021 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1672A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1672 | chr10 | 102631827 | |||||
| chr10:102631830
|
G | A | 1 | a0001c0001t0012 | 2 | HG00735.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1675G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1675 | chr10 | 102631830 | |||||
| chr10:102631870
|
A | G | 9 | a0001c0002t0002a0001c0002t0007a0001c0002t0025others(6): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1715A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1715 | chr10 | 102631870 | |||||
| chr10:102631875
|
C | T | 1 | a0001c0001t0020 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1720C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1720 | chr10 | 102631875 | |||||
| chr10:102632044
|
C | G | 1 | a0001c0001t0011 | 2 | HG02257.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1889C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1889 | chr10 | 102632044 | |||||
| chr10:102632091
|
C | T | 1 | a0001c0001t0019 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 1936 | chr10 | 102632091 | |||||
| chr10:102632250
|
T | C | 1 | a0001c0001t0023 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2095T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2095 | chr10 | 102632250 | |||||
| chr10:102632295
|
G | T | 1 | a0001c0001t0018 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2140G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2140 | chr10 | 102632295 | |||||
| chr10:102632345
|
C | T | 1 | a0001c0002t0030 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2190 | chr10 | 102632345 | |||||
| chr10:102632348
|
A | G | 1 | a0001c0001t0011 | 2 | HG02257.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2193A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2193 | chr10 | 102632348 | |||||
| chr10:102632740
|
T | C | 13 | a0001c0001t0006a0001c0001t0008a0001c0001t0012others(10): Show | 93 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2585T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2585 | chr10 | 102632740 | |||||
| chr10:102632761
|
C | CTGGTGCT others(34): Show |
1 | a0001c0002t0029 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2609_*2649dupGTGC others(37): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2650 | INFO_REALIGN_3_PRIME | chr10 | 102632761 | ||||
| chr10:102632823
|
C | T | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0022others(4): Show | 30 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2668C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2668 | chr10 | 102632823 | |||||
| chr10:102632884
|
T | C | 1 | a0001c0002t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 2729 | chr10 | 102632884 | |||||
| chr10:102633241
|
A | G | 3 | a0001c0001t0010a0001c0001t0033a0001c0001t0034 | 4 | HG02486.hp2 HG02717.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3086A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3086 | chr10 | 102633241 | |||||
| chr10:102633423
|
G | C | 1 | a0001c0001t0017 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3268 | chr10 | 102633423 | |||||
| chr10:102633445
|
C | G | 1 | a0001c0001t0009 | 2 | HG00741.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3290C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3290 | chr10 | 102633445 | |||||
| chr10:102633501
|
C | T | 1 | a0001c0002t0028 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3346C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3346 | chr10 | 102633501 | |||||
| chr10:102633509
|
C | T | 1 | a0001c0002t0027 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3354C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3354 | chr10 | 102633509 | |||||
| chr10:102633511
|
G | T | 1 | a0001c0002t0007 | 5 | HG02451.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3356G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 12/12 | 3356 | chr10 | 102633511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102504350
|
C | T | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.182+16C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504350 | ||||||
| chr10:102504523
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.182+189C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504523 | ||||||
| chr10:102504684
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.182+350G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504684 | ||||||
| chr10:102504723
|
C | G | 1 | a0001c0001t0008g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.182+389C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504723 | ||||||
| chr10:102504753
|
G | A | 5 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(2): Show | 5 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+419G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504753 | ||||||
| chr10:102504856
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.182+522G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504856 | ||||||
| chr10:102504879
|
G | GTCTCCTT others(32): Show |
1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.182+548_182+586dup others(39): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102504879 | |||||
| chr10:102504957
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182+623G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102504957 | ||||||
| chr10:102505284
|
C | T | 4 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(1): Show | 4 | HG01070.hp2 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+950C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102505284 | ||||||
| chr10:102505290
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.182+956C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102505290 | ||||||
| chr10:102506039
|
G | GA | 25 | a0001c0001t0001g0179a0001c0001t0003g0181a0001c0001t0003g0182others(22): Show | 25 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.182+1732dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102506039 | |||||
| chr10:102506039
|
GA | G | 80 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0124others(77): Show | 80 | HG00280.hp1 HG00733.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.182+1732delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102506039 | |||||
| chr10:102506040
|
A | G | 9 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(6): Show | 9 | HG01175.hp2 HG01928.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+1706A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506040 | ||||||
| chr10:102506041
|
A | G | 70 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0124others(67): Show | 70 | HG00280.hp1 HG00733.hp1 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.182+1707A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506041 | ||||||
| chr10:102506042
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0004g0110 | 2 | HG01069.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.182+1708A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506042 | ||||||
| chr10:102506047
|
A | G | 1 | a0001c0001t0004g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.182+1713A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506047 | ||||||
| chr10:102506473
|
G | C | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.182+2139G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506473 | ||||||
| chr10:102506477
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2143C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506477 | ||||||
| chr10:102506482
|
G | A | 33 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(30): Show | 33 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.182+2148G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506482 | ||||||
| chr10:102506502
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG00735.hp2 HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.182+2168C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506502 | ||||||
| chr10:102506513
|
A | G | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG00558.hp2 HG02056.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+2179A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506513 | ||||||
| chr10:102506527
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18955.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.182+2193C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506527 | ||||||
| chr10:102506656
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.182+2322G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506656 | ||||||
| chr10:102506733
|
A | G | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2399A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506733 | ||||||
| chr10:102506804
|
G | A | 5 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-2365G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102506804 | ||||||
| chr10:102507034
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.183-2135C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102507034 | ||||||
| chr10:102507046
|
C | T | 2 | a0001c0002t0002g0087a0001c0002t0028g0086 | 2 | HG01993.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.183-2123C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102507046 | ||||||
| chr10:102507474
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183-1695A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102507474 | ||||||
| chr10:102507961
|
A | AT | 19 | a0001c0001t0001g0071a0001c0001t0001g0207a0001c0001t0005g0020others(16): Show | 19 | HG01074.hp1 HG01081.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.183-1185dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102507961 | |||||
| chr10:102507961
|
AT | A | 17 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0211others(14): Show | 17 | HG01070.hp1 HG01891.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.183-1185delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102507961 | |||||
| chr10:102507961
|
ATT | A | 72 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(69): Show | 72 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.183-1186_183-1185d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 102507961 | |||||
| chr10:102508024
|
G | A | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.183-1145G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508024 | ||||||
| chr10:102508101
|
T | A | 1 | a0001c0002t0002g0023 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.183-1068T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508101 | ||||||
| chr10:102508364
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.183-805C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508364 | ||||||
| chr10:102508420
|
C | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.183-749C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508420 | ||||||
| chr10:102508747
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.183-422C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508747 | ||||||
| chr10:102508869
|
T | C | 54 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(51): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.183-300T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102508869 | ||||||
| chr10:102509043
|
G | C | 266 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(263): Show |
intron_variant | MODIFIER | c.183-126G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102509043 | ||||||
| chr10:102509101
|
AG | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.183-67delG | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102509101 | ||||||
| chr10:102509103
|
C | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.183-66C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102509103 | ||||||
| chr10:102509120
|
G | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.183-49G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 1/11 | chr10 | 102509120 | ||||||
| chr10:102509460
|
G | A | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.317+157G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102509460 | ||||||
| chr10:102509544
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+241G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102509544 | ||||||
| chr10:102509591
|
C | G | 1 | a0001c0001t0024g0252 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.317+288C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102509591 | ||||||
| chr10:102509918
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.317+615G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102509918 | ||||||
| chr10:102510248
|
T | G | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+945T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510248 | ||||||
| chr10:102510457
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+1154C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510457 | ||||||
| chr10:102510460
|
G | A | 54 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(51): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.317+1157G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510460 | ||||||
| chr10:102510491
|
A | AG | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+1188_317+1189i others(3): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510491 | ||||||
| chr10:102510493
|
G | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+1190G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510493 | ||||||
| chr10:102510502
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.317+1199C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510502 | ||||||
| chr10:102510601
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+1298C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510601 | ||||||
| chr10:102510619
|
C | T | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.317+1316C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510619 | ||||||
| chr10:102510716
|
C | T | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.317+1413C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102510716 | ||||||
| chr10:102511024
|
G | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+1721G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511024 | ||||||
| chr10:102511121
|
CA | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0254a0001c0001t0006g0251others(3): Show | 6 | HG00558.hp1 HG01993.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+1834delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102511121 | |||||
| chr10:102511138
|
GTAA | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+1855_317+1857d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102511138 | |||||
| chr10:102511141
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.317+1838A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511141 | ||||||
| chr10:102511335
|
C | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+2032C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511335 | ||||||
| chr10:102511518
|
T | C | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.317+2215T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511518 | ||||||
| chr10:102511546
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+2243G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511546 | ||||||
| chr10:102511586
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0206 | 2 | NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.317+2283C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511586 | ||||||
| chr10:102511628
|
G | C | 13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+2325G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511628 | ||||||
| chr10:102511917
|
G | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+2614G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102511917 | ||||||
| chr10:102512123
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.317+2820T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512123 | ||||||
| chr10:102512266
|
A | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+2963A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512266 | ||||||
| chr10:102512579
|
T | C | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+3276T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512579 | ||||||
| chr10:102512697
|
C | T | 1 | a0001c0002t0025g0065 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.317+3394C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512697 | ||||||
| chr10:102512945
|
G | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+3642G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512945 | ||||||
| chr10:102512953
|
A | T | 6 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+3650A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102512953 | ||||||
| chr10:102513032
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+3729C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513032 | ||||||
| chr10:102513078
|
T | G | 1 | a0001c0002t0002g0001 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.317+3775T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513078 | ||||||
| chr10:102513135
|
G | T | 1 | a0001c0002t0002g0064 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.317+3832G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513135 | ||||||
| chr10:102513155
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.317+3852A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513155 | ||||||
| chr10:102513571
|
G | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+4268G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513571 | ||||||
| chr10:102513595
|
C | T | 2 | a0001c0001t0013g0248a0001c0001t0013g0249 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.317+4292C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513595 | ||||||
| chr10:102513814
|
T | C | 1 | a0001c0001t0005g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.317+4511T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513814 | ||||||
| chr10:102513856
|
A | C | 1 | a0001c0002t0002g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.317+4553A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513856 | ||||||
| chr10:102513880
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.317+4577T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513880 | ||||||
| chr10:102513880
|
T | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+4577T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513880 | ||||||
| chr10:102513894
|
T | A | 1 | a0001c0002t0002g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.317+4591T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102513894 | ||||||
| chr10:102514106
|
C | T | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+4803C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514106 | ||||||
| chr10:102514133
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+4830T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514133 | ||||||
| chr10:102514186
|
A | G | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+4883A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514186 | ||||||
| chr10:102514188
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.317+4885C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514188 | ||||||
| chr10:102514194
|
T | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.317+4891T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514194 | ||||||
| chr10:102514310
|
C | T | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+5007C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514310 | ||||||
| chr10:102514400
|
C | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+5097C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514400 | ||||||
| chr10:102514504
|
G | C | 1 | a0001c0001t0004g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.317+5201G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514504 | ||||||
| chr10:102514572
|
G | C | 54 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(51): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.317+5269G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514572 | ||||||
| chr10:102514666
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.317+5363G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514666 | ||||||
| chr10:102514708
|
C | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+5405C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514708 | ||||||
| chr10:102514709
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+5406T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514709 | ||||||
| chr10:102514786
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+5483T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514786 | ||||||
| chr10:102514837
|
C | T | 1 | a0001c0001t0001g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.317+5534C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514837 | ||||||
| chr10:102514973
|
C | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+5670C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102514973 | ||||||
| chr10:102515061
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+5758G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515061 | ||||||
| chr10:102515068
|
G | A | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+5765G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515068 | ||||||
| chr10:102515308
|
G | A | 2 | a0001c0001t0013g0248a0001c0001t0013g0249 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.317+6005G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515308 | ||||||
| chr10:102515315
|
C | CT | 59 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0175others(56): Show | 59 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.317+6031dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102515315 | |||||
| chr10:102515315
|
CT | C | 6 | a0001c0001t0001g0109a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG01069.hp1 HG06807.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+6031delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102515315 | |||||
| chr10:102515350
|
T | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0123others(1): Show | 4 | HG02922.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+6047T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515350 | ||||||
| chr10:102515661
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+6358C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515661 | ||||||
| chr10:102515986
|
C | T | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | HG02280.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+6683C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515986 | ||||||
| chr10:102515988
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.317+6685G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102515988 | ||||||
| chr10:102516097
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.317+6794A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516097 | ||||||
| chr10:102516125
|
C | CT | 20 | a0001c0001t0001g0071a0001c0001t0005g0020a0001c0001t0005g0021others(17): Show | 20 | HG01074.hp1 HG01081.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.317+6840dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102516125 | |||||
| chr10:102516125
|
C | CTTT | 85 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(82): Show | 85 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.317+6838_317+6840d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102516125 | |||||
| chr10:102516125
|
CTT | C | 10 | a0001c0001t0001g0166a0001c0002t0002g0098a0001c0002t0002g0099others(7): Show | 10 | HG01358.hp1 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.317+6839_317+6840d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102516125 | |||||
| chr10:102516125
|
CTTT | C | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.317+6838_317+6840d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102516125 | |||||
| chr10:102516206
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.317+6903G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516206 | ||||||
| chr10:102516224
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.317+6921G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516224 | ||||||
| chr10:102516224
|
G | C | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+6921G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516224 | ||||||
| chr10:102516236
|
G | A | 4 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(1): Show | 4 | HG01070.hp2 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+6933G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516236 | ||||||
| chr10:102516286
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+6983C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516286 | ||||||
| chr10:102516315
|
C | T | 13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+7012C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516315 | ||||||
| chr10:102516421
|
A | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.317+7118A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516421 | ||||||
| chr10:102516553
|
A | G | 1 | a0001c0005t0004g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.317+7250A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516553 | ||||||
| chr10:102516767
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+7464C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516767 | ||||||
| chr10:102516898
|
C | T | 1 | a0001c0001t0004g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.317+7595C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516898 | ||||||
| chr10:102516987
|
G | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+7684G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102516987 | ||||||
| chr10:102517045
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+7742T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517045 | ||||||
| chr10:102517311
|
A | G | 1 | a0001c0001t0003g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.317+8008A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517311 | ||||||
| chr10:102517336
|
G | A | 21 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(18): Show | 21 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.317+8033G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517336 | ||||||
| chr10:102517366
|
A | C | 54 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(51): Show | 54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.317+8063A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517366 | ||||||
| chr10:102517386
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0008g0022a0001c0001t0008g0092 | 3 | HG01516.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+8083C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517386 | ||||||
| chr10:102517623
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+8320T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517623 | ||||||
| chr10:102517683
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+8380T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517683 | ||||||
| chr10:102517848
|
C | T | 1 | a0001c0002t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.317+8545C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102517848 | ||||||
| chr10:102518298
|
A | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+8995A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518298 | ||||||
| chr10:102518515
|
G | GTCTA | 9 | a0001c0001t0001g0247a0001c0001t0003g0183a0001c0001t0003g0237others(6): Show | 9 | HG00741.hp2 HG01081.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+9215_317+9216i others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518515 | |||||
| chr10:102518515
|
G | GTCTATCT others(1): Show |
40 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0196others(37): Show | 40 | HG00558.hp2 HG00639.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.317+9215_317+9216i others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518515 | |||||
| chr10:102518515
|
G | GTCTATCT others(5): Show |
31 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(28): Show | 31 | HG00558.hp1 HG00597.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.317+9215_317+9216i others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518515 | |||||
| chr10:102518515
|
G | GTCTATCT others(9): Show |
8 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0215others(5): Show | 8 | HG01192.hp1 HG02300.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+9215_317+9216i others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518515 | |||||
| chr10:102518515
|
G | GTCTATCT others(13): Show |
1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.317+9215_317+9216i others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518515 | |||||
| chr10:102518519
|
G | A | 90 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.317+9216G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518519 | ||||||
| chr10:102518519
|
G | GTCTA | 4 | a0001c0001t0008g0022a0001c0001t0014g0017a0001c0001t0014g0018others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+9242_317+9245d others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518519
|
G | GTCTATCT others(1): Show |
78 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.317+9238_317+9245d others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518519
|
G | GTCTATCT others(5): Show |
56 | a0001c0001t0001g0071a0001c0001t0001g0111a0001c0001t0001g0112others(53): Show | 56 | HG00544.hp1 HG00733.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.317+9234_317+9245d others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518519
|
G | GTCTATCT others(9): Show |
26 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(23): Show | 26 | HG00544.hp2 HG01952.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.317+9230_317+9245d others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518519
|
G | GTCTATCT others(13): Show |
11 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0132others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+9226_317+9245d others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518519
|
G | GTCTATCT others(17): Show |
2 | a0001c0001t0001g0115a0001c0002t0002g0002 | 2 | HG01175.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.317+9222_317+9245d others(26): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102518519 | |||||
| chr10:102518549
|
T | C | 76 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0184others(73): Show | 76 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.317+9246T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518549 | ||||||
| chr10:102518827
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0016g0191 | 2 | NA18960.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.317+9524G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518827 | ||||||
| chr10:102518844
|
T | C | 45 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(42): Show | 45 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.317+9541T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518844 | ||||||
| chr10:102518861
|
C | T | 45 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(42): Show | 45 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.317+9558C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518861 | ||||||
| chr10:102518936
|
G | A | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.317+9633G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102518936 | ||||||
| chr10:102519002
|
G | A | 18 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.317+9699G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519002 | ||||||
| chr10:102519096
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.317+9793C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519096 | ||||||
| chr10:102519137
|
C | CAA | 90 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(87): Show | 90 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.317+9851_317+9852d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102519137 | |||||
| chr10:102519137
|
CA | C | 9 | a0001c0001t0001g0147a0001c0002t0002g0098a0001c0002t0002g0099others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.317+9852delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102519137 | |||||
| chr10:102519422
|
G | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+10119G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519422 | ||||||
| chr10:102519527
|
C | CA | 109 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(106): Show | 109 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.317+10241dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102519527 | |||||
| chr10:102519527
|
C | CAAA | 60 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(57): Show | 60 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.317+10239_317+1024 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102519527 | |||||
| chr10:102519527
|
C | CAAAA | 22 | a0001c0001t0001g0115a0001c0001t0004g0093a0001c0001t0004g0094others(19): Show | 22 | HG01175.hp2 HG01928.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.317+10238_317+1024 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102519527 | |||||
| chr10:102519589
|
A | T | 15 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(12): Show | 15 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.317+10286A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519589 | ||||||
| chr10:102519637
|
G | A | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.317+10334G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519637 | ||||||
| chr10:102519833
|
A | G | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+10530A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519833 | ||||||
| chr10:102519906
|
G | T | 1 | a0001c0001t0005g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.317+10603G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102519906 | ||||||
| chr10:102520089
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.317+10786A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520089 | ||||||
| chr10:102520120
|
C | A | 1 | a0001c0002t0002g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.317+10817C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520120 | ||||||
| chr10:102520212
|
C | CT | 21 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0074others(18): Show | 21 | HG01074.hp1 HG01891.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.317+10931dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102520212 | |||||
| chr10:102520212
|
CT | C | 70 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0184others(67): Show | 70 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.317+10931delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102520212 | |||||
| chr10:102520212
|
CTTT | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+10929_317+1093 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102520212 | |||||
| chr10:102520212
|
CTTTT | C | 72 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(69): Show | 72 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.317+10928_317+1093 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102520212 | |||||
| chr10:102520212
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0189 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317+10921_317+1093 others(15): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102520212 | |||||
| chr10:102520216
|
T | C | 2 | a0001c0002t0002g0011a0001c0002t0002g0028 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.317+10913T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520216 | ||||||
| chr10:102520217
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.317+10914T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520217 | ||||||
| chr10:102520219
|
T | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+10916T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520219 | ||||||
| chr10:102520220
|
T | C | 72 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(69): Show | 72 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.317+10917T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520220 | ||||||
| chr10:102520221
|
T | C | 2 | a0001c0001t0004g0131a0001c0005t0004g0165 | 2 | NA18954.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.317+10918T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520221 | ||||||
| chr10:102520281
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.317+10978G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520281 | ||||||
| chr10:102520355
|
C | A | 1 | a0001c0002t0002g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.317+11052C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520355 | ||||||
| chr10:102520367
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.317+11064G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520367 | ||||||
| chr10:102520473
|
G | A | 4 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0074others(1): Show | 4 | HG01891.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+11170G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520473 | ||||||
| chr10:102520481
|
A | C | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+11178A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520481 | ||||||
| chr10:102520712
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.317+11409A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520712 | ||||||
| chr10:102520733
|
T | C | 1 | a0001c0001t0004g0093 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.317+11430T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520733 | ||||||
| chr10:102520780
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+11477G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520780 | ||||||
| chr10:102520793
|
A | T | 2 | a0001c0001t0006g0216a0001c0001t0006g0261 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.317+11490A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520793 | ||||||
| chr10:102520809
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.317+11506C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520809 | ||||||
| chr10:102520907
|
G | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+11604G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520907 | ||||||
| chr10:102520926
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.317+11623A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102520926 | ||||||
| chr10:102521055
|
T | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0245a0001c0001t0018g0241 | 3 | HG01070.hp1 HG01071.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.317+11752T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521055 | ||||||
| chr10:102521084
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.317+11781C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521084 | ||||||
| chr10:102521398
|
C | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+12095C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521398 | ||||||
| chr10:102521482
|
G | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+12179G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521482 | ||||||
| chr10:102521940
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0169 | 3 | NA19011.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.317+12637C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521940 | ||||||
| chr10:102521983
|
A | G | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+12680A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102521983 | ||||||
| chr10:102522098
|
C | T | 1 | a0001c0001t0022g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.317+12795C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522098 | ||||||
| chr10:102522205
|
C | T | 2 | a0001c0001t0012g0236a0001c0001t0012g0262 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.317+12902C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522205 | ||||||
| chr10:102522403
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+13100G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522403 | ||||||
| chr10:102522508
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+13205T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522508 | ||||||
| chr10:102522661
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+13358T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522661 | ||||||
| chr10:102522980
|
A | T | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+13677A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102522980 | ||||||
| chr10:102523104
|
G | A | 69 | a0001c0001t0001g0071a0001c0001t0003g0031a0001c0001t0003g0032others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+13801G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523104 | ||||||
| chr10:102523226
|
G | C | 18 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.317+13923G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523226 | ||||||
| chr10:102523408
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+14105G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523408 | ||||||
| chr10:102523579
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0172 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.317+14276G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523579 | ||||||
| chr10:102523715
|
G | C | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+14412G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523715 | ||||||
| chr10:102523753
|
G | A | 6 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(3): Show | 6 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+14450G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102523753 | ||||||
| chr10:102524117
|
C | A | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.317+14814C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524117 | ||||||
| chr10:102524260
|
C | G | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.317+14957C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524260 | ||||||
| chr10:102524295
|
G | A | 1 | a0001c0002t0002g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.317+14992G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524295 | ||||||
| chr10:102524324
|
C | CT | 4 | a0001c0001t0012g0262a0001c0002t0002g0060a0001c0002t0002g0061others(1): Show | 4 | HG01175.hp1 NA18959.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+15025dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102524324 | |||||
| chr10:102524328
|
TC | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+15026delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524328 | ||||||
| chr10:102524329
|
C | T | 182 | a0001c0001t0001g0071a0001c0001t0001g0176a0001c0001t0001g0177others(179): Show | 182 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.317+15026C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524329 | ||||||
| chr10:102524509
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.317+15206A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524509 | ||||||
| chr10:102524653
|
G | A | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+15350G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524653 | ||||||
| chr10:102524691
|
C | T | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+15388C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524691 | ||||||
| chr10:102524753
|
C | A | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.317+15450C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524753 | ||||||
| chr10:102524903
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.317+15600C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524903 | ||||||
| chr10:102525329
|
C | T | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.317+16026C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102525329 | ||||||
| chr10:102525481
|
C | T | 1 | a0001c0001t0006g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.317+16178C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102525481 | ||||||
| chr10:102525743
|
A | G | 18 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.317+16440A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102525743 | ||||||
| chr10:102525837
|
A | T | 95 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(92): Show | 95 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.317+16534A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102525837 | ||||||
| chr10:102526103
|
C | T | 2 | a0001c0002t0002g0058a0001c0002t0002g0059 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.317+16800C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102526103 | ||||||
| chr10:102526355
|
G | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+17052G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102526355 | ||||||
| chr10:102526363
|
G | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+17060G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102526363 | ||||||
| chr10:102526420
|
G | T | 1 | a0001c0001t0004g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.317+17117G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102526420 | ||||||
| chr10:102526993
|
G | GT | 21 | a0001c0001t0001g0195a0001c0001t0001g0215a0001c0001t0003g0181others(18): Show | 21 | HG00597.hp2 HG01175.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.317+17711dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102526993 | |||||
| chr10:102526993
|
GT | G | 82 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0113others(79): Show | 82 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.317+17711delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102526993 | |||||
| chr10:102527065
|
C | T | 1 | a0001c0002t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.317+17762C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527065 | ||||||
| chr10:102527079
|
TG | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0009g0189others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+17777delG | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527079 | ||||||
| chr10:102527291
|
C | T | 38 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(35): Show | 38 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.317+17988C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527291 | ||||||
| chr10:102527294
|
G | A | 38 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(35): Show | 38 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.317+17991G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527294 | ||||||
| chr10:102527498
|
G | GAT | 38 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(35): Show | 38 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.317+18210_317+1821 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102527498 | |||||
| chr10:102527498
|
G | GATAT | 53 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0211others(50): Show | 53 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.317+18208_317+1821 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102527498 | |||||
| chr10:102527498
|
G | GATATAT | 36 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(33): Show | 36 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.317+18206_317+1821 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102527498 | |||||
| chr10:102527498
|
G | GATATATA others(1): Show |
9 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0212others(6): Show | 9 | HG01169.hp2 HG01258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+18204_317+1821 others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102527498 | |||||
| chr10:102527500
|
T | G | 1 | a0001c0002t0002g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.317+18197T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527500 | ||||||
| chr10:102527602
|
T | G | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.317+18299T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527602 | ||||||
| chr10:102527763
|
A | AT | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+18460_317+1846 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102527763 | ||||||
| chr10:102528317
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.317+19014C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528317 | ||||||
| chr10:102528322
|
C | A | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+19019C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528322 | ||||||
| chr10:102528495
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.317+19192A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528495 | ||||||
| chr10:102528606
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.317+19303C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528606 | ||||||
| chr10:102528623
|
A | C | 4 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0061others(1): Show | 4 | NA18961.hp2 NA18962.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+19320A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528623 | ||||||
| chr10:102528638
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.317+19335C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528638 | ||||||
| chr10:102528961
|
C | CT | 46 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0176others(43): Show | 46 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.317+19675dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102528961 | |||||
| chr10:102528961
|
C | CTT | 47 | a0001c0001t0001g0190a0001c0001t0001g0232a0001c0001t0001g0242others(44): Show | 47 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.317+19674_317+1967 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102528961 | |||||
| chr10:102528961
|
CT | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0004g0096others(10): Show | 13 | HG01943.hp2 HG01993.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+19675delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102528961 | |||||
| chr10:102528967
|
T | C | 5 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+19664T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102528967 | ||||||
| chr10:102529007
|
C | CTG | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.317+19704_317+1970 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529007 | ||||||
| chr10:102529019
|
G | T | 4 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(1): Show | 4 | HG01070.hp2 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+19716G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529019 | ||||||
| chr10:102529020
|
T | G | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.317+19717T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529020 | ||||||
| chr10:102529241
|
G | A | 1 | a0001c0002t0002g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.317+19938G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529241 | ||||||
| chr10:102529255
|
G | T | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.317+19952G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529255 | ||||||
| chr10:102529397
|
A | G | 1 | a0001c0001t0003g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.317+20094A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529397 | ||||||
| chr10:102529746
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.318-20224A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529746 | ||||||
| chr10:102529853
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.318-20117G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529853 | ||||||
| chr10:102529901
|
CGCCACTG others(1303): Show |
C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0169 | 3 | NA19011.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.318-20050_318-1874 others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102529901 | |||||
| chr10:102529943
|
C | CA | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-20014dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102529943 | |||||
| chr10:102529981
|
C | G | 4 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082others(1): Show | 4 | HG01074.hp1 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-19989C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102529981 | ||||||
| chr10:102530049
|
A | G | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.318-19921A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102530049 | ||||||
| chr10:102530323
|
C | A | 1 | a0001c0001t0034g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-19647C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102530323 | ||||||
| chr10:102530447
|
CT | C | 99 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0113others(96): Show | 99 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.318-19502delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102530447 | |||||
| chr10:102530447
|
CTTT | C | 93 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.318-19504_318-1950 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102530447 | |||||
| chr10:102530636
|
T | C | 2 | a0001c0002t0026g0036a0001c0002t0029g0037 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.318-19334T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102530636 | ||||||
| chr10:102530654
|
A | C | 1 | a0001c0002t0002g0057 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.318-19316A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102530654 | ||||||
| chr10:102530705
|
C | T | 78 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(75): Show | 78 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.318-19265C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102530705 | ||||||
| chr10:102531046
|
C | T | 2 | a0001c0001t0013g0248a0001c0001t0013g0249 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.318-18924C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102531046 | ||||||
| chr10:102531082
|
C | CA | 6 | a0001c0002t0002g0099a0001c0002t0002g0100a0001c0002t0002g0101others(3): Show | 6 | HG01891.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-18866dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531082 | |||||
| chr10:102531082
|
CA | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-18866delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531082 | |||||
| chr10:102531082
|
CAA | C | 163 | a0001c0001t0001g0071a0001c0001t0001g0118a0001c0001t0001g0133others(160): Show | 163 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.318-18867_318-1886 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531082 | |||||
| chr10:102531082
|
CAAA | C | 10 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(7): Show | 10 | HG02040.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-18868_318-1886 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531082 | |||||
| chr10:102531211
|
T | C | 18 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-18759T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102531211 | ||||||
| chr10:102531490
|
G | A | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318-18480G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102531490 | ||||||
| chr10:102531658
|
CA | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.318-18309delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531658 | |||||
| chr10:102531703
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0214 | 2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.318-18267A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102531703 | ||||||
| chr10:102531959
|
C | CT | 84 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(81): Show | 84 | HG00280.hp1 HG00733.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.318-17998dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102531959 | |||||
| chr10:102532142
|
A | T | 1 | a0001c0001t0015g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.318-17828A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102532142 | ||||||
| chr10:102532198
|
C | G | 1 | a0001c0001t0019g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.318-17772C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102532198 | ||||||
| chr10:102532248
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.318-17722C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102532248 | ||||||
| chr10:102532379
|
C | T | 1 | a0001c0001t0010g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.318-17591C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102532379 | ||||||
| chr10:102533079
|
A | G | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318-16891A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533079 | ||||||
| chr10:102533225
|
T | C | 1 | a0001c0002t0002g0015 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.318-16745T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533225 | ||||||
| chr10:102533300
|
G | A | 3 | a0001c0001t0010g0052a0001c0002t0026g0036a0001c0002t0029g0037 | 3 | HG02615.hp2 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.318-16670G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533300 | ||||||
| chr10:102533319
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0009g0189others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-16651C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533319 | ||||||
| chr10:102533370
|
G | A | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.318-16600G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533370 | ||||||
| chr10:102533408
|
C | CA | 9 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0187others(6): Show | 9 | HG00597.hp1 HG00741.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.318-16546dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102533408 | |||||
| chr10:102533500
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.318-16470A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533500 | ||||||
| chr10:102533567
|
C | T | 3 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0250 | 3 | HG02071.hp2 NA18946.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.318-16403C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533567 | ||||||
| chr10:102533583
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.318-16387C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533583 | ||||||
| chr10:102533637
|
T | C | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-16333T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533637 | ||||||
| chr10:102533655
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-16315C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533655 | ||||||
| chr10:102533704
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-16266G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533704 | ||||||
| chr10:102533852
|
A | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-16118A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102533852 | ||||||
| chr10:102533922
|
CTCT | C | 15 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.318-16042_318-1604 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102533922 | |||||
| chr10:102534097
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.318-15873C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534097 | ||||||
| chr10:102534224
|
C | T | 1 | a0001c0002t0007g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.318-15746C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534224 | ||||||
| chr10:102534319
|
T | C | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0235others(1): Show | 4 | NA18943.hp2 NA18983.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-15651T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534319 | ||||||
| chr10:102534322
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.318-15648G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534322 | ||||||
| chr10:102534471
|
C | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-15499C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534471 | ||||||
| chr10:102534595
|
A | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-15375A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534595 | ||||||
| chr10:102534627
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.318-15343G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534627 | ||||||
| chr10:102534727
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.318-15243G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534727 | ||||||
| chr10:102534874
|
C | T | 1 | a0001c0002t0028g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.318-15096C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534874 | ||||||
| chr10:102534908
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-15062C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102534908 | ||||||
| chr10:102535398
|
A | G | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-14572A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535398 | ||||||
| chr10:102535479
|
C | A | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG00280.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.318-14491C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535479 | ||||||
| chr10:102535484
|
C | CA | 81 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(78): Show | 81 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.318-14472dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535484 | |||||
| chr10:102535625
|
C | T | 42 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(39): Show | 42 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.318-14345C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535625 | ||||||
| chr10:102535645
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-14325T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535645 | ||||||
| chr10:102535646
|
A | G | 2 | a0001c0001t0006g0216a0001c0001t0006g0261 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.318-14324A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535646 | ||||||
| chr10:102535653
|
C | G | 1 | a0001c0001t0019g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.318-14317C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535653 | ||||||
| chr10:102535686
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.318-14284T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535686 | ||||||
| chr10:102535860
|
C | T | 1 | a0001c0001t0004g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.318-14110C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535860 | ||||||
| chr10:102535930
|
A | AGAT | 56 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(53): Show | 56 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.318-14002_318-1400 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535930 | |||||
| chr10:102535930
|
A | AGATGAT | 23 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0198others(20): Show | 23 | HG00639.hp1 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.318-14005_318-1400 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535930 | |||||
| chr10:102535930
|
A | AGATGATG others(2): Show |
4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(1): Show | 4 | HG01433.hp1 HG02071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-14008_318-1400 others(13): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535930 | |||||
| chr10:102535930
|
AGAT | A | 10 | a0001c0001t0011g0067a0001c0002t0002g0098a0001c0002t0002g0099others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-14002_318-1400 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535930 | |||||
| chr10:102535930
|
AGATGATG others(2): Show |
A | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.318-14008_318-1400 others(13): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102535930 | |||||
| chr10:102535977
|
A | T | 4 | a0001c0002t0002g0023a0001c0002t0002g0035a0001c0002t0002g0039others(1): Show | 4 | HG02735.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-13993A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102535977 | ||||||
| chr10:102536288
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.318-13682A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536288 | ||||||
| chr10:102536289
|
G | C | 11 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0186others(8): Show | 11 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.318-13681G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536289 | ||||||
| chr10:102536317
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318-13653G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536317 | ||||||
| chr10:102536363
|
CT | C | 222 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0001g0113others(219): Show | 222 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.318-13588delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102536363 | |||||
| chr10:102536425
|
G | A | 1 | a0001c0001t0034g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-13545G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536425 | ||||||
| chr10:102536456
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-13514C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536456 | ||||||
| chr10:102536632
|
G | A | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318-13338G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536632 | ||||||
| chr10:102536661
|
C | G | 22 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0184others(19): Show | 22 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.318-13309C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536661 | ||||||
| chr10:102536662
|
T | G | 22 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0184others(19): Show | 22 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.318-13308T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536662 | ||||||
| chr10:102536712
|
T | A | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-13258T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536712 | ||||||
| chr10:102536847
|
G | T | 1 | a0001c0002t0002g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.318-13123G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536847 | ||||||
| chr10:102536879
|
T | C | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-13091T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536879 | ||||||
| chr10:102536887
|
G | A | 1 | a0001c0002t0002g0011 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.318-13083G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536887 | ||||||
| chr10:102537129
|
C | CT | 10 | a0001c0001t0001g0176a0001c0001t0001g0198a0001c0001t0005g0020others(7): Show | 10 | HG02056.hp1 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-12820dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102537129 | |||||
| chr10:102537129
|
CT | C | 70 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0116others(67): Show | 70 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.318-12820delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102537129 | |||||
| chr10:102537129
|
CTT | C | 15 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0123others(12): Show | 15 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.318-12821_318-1282 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102537129 | |||||
| chr10:102537173
|
C | T | 1 | a0001c0001t0010g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318-12797C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102537173 | ||||||
| chr10:102537254
|
C | T | 1 | a0001c0002t0027g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.318-12716C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102537254 | ||||||
| chr10:102537293
|
G | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-12677G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102537293 | ||||||
| chr10:102537606
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-12364C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102537606 | ||||||
| chr10:102538034
|
T | C | 194 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(191): Show |
intron_variant | MODIFIER | c.318-11936T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538034 | ||||||
| chr10:102538198
|
C | T | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-11772C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538198 | ||||||
| chr10:102538349
|
C | CT | 82 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(79): Show | 82 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.318-11611dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102538349 | |||||
| chr10:102538642
|
CAT | C | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.318-11327_318-1132 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538642 | ||||||
| chr10:102538660
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.318-11310C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538660 | ||||||
| chr10:102538715
|
T | A | 1 | a0001c0001t0005g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.318-11255T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538715 | ||||||
| chr10:102538735
|
A | C | 1 | a0001c0001t0003g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.318-11235A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538735 | ||||||
| chr10:102538781
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.318-11189G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538781 | ||||||
| chr10:102538920
|
G | T | 1 | a0001c0001t0010g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318-11050G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538920 | ||||||
| chr10:102539172
|
A | C | 1 | a0001c0002t0028g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.318-10798A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102539172 | ||||||
| chr10:102539293
|
G | A | 1 | a0001c0002t0002g0001 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.318-10677G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102539293 | ||||||
| chr10:102539434
|
ATTGT | A | 56 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(53): Show | 56 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.318-10532_318-1052 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102539434 | |||||
| chr10:102539507
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-10463G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102539507 | ||||||
| chr10:102539693
|
G | A | 1 | a0001c0003t0003g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.318-10277G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102539693 | ||||||
| chr10:102540111
|
T | G | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-9859T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540111 | ||||||
| chr10:102540219
|
C | T | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.318-9751C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540219 | ||||||
| chr10:102540717
|
A | AAT | 4 | a0001c0001t0008g0022a0001c0001t0008g0092a0001c0002t0002g0053others(1): Show | 4 | HG02040.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-9236_318-9235d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102540717 | |||||
| chr10:102540717
|
AAT | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-9236_318-9235d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102540717 | |||||
| chr10:102540847
|
C | A | 1 | a0001c0001t0003g0227 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.318-9123C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540847 | ||||||
| chr10:102540881
|
C | G | 194 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(191): Show |
intron_variant | MODIFIER | c.318-9089C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540881 | ||||||
| chr10:102540883
|
G | A | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-9087G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540883 | ||||||
| chr10:102540951
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.318-9019G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102540951 | ||||||
| chr10:102541022
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0173 | 2 | HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.318-8948G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541022 | ||||||
| chr10:102541054
|
C | T | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-8916C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541054 | ||||||
| chr10:102541222
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-8748C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541222 | ||||||
| chr10:102541406
|
TC | T | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-8563delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541406 | ||||||
| chr10:102541555
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.318-8415C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541555 | ||||||
| chr10:102541556
|
G | A | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-8414G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541556 | ||||||
| chr10:102541650
|
C | T | 6 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0034others(3): Show | 6 | HG02273.hp1 HG02300.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-8320C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541650 | ||||||
| chr10:102541669
|
G | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318-8301G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541669 | ||||||
| chr10:102541697
|
C | CT | 38 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0185others(35): Show | 38 | HG00544.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.318-8249dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541697 | |||||
| chr10:102541697
|
C | CTT | 55 | a0001c0001t0001g0109a0001c0001t0001g0167a0001c0001t0001g0168others(52): Show | 55 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.318-8250_318-8249d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541697 | |||||
| chr10:102541697
|
C | CTTT | 60 | a0001c0001t0001g0112a0001c0001t0001g0118a0001c0001t0001g0123others(57): Show | 60 | HG00280.hp1 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.318-8251_318-8249d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541697 | |||||
| chr10:102541697
|
C | CTTTT | 25 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.318-8252_318-8249d others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541697 | |||||
| chr10:102541697
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0164 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.318-8258_318-8249d others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541697 | |||||
| chr10:102541875
|
A | AT | 41 | a0001c0001t0001g0177a0001c0001t0001g0187a0001c0001t0001g0232others(38): Show | 41 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.318-8072dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541875 | |||||
| chr10:102541875
|
A | ATT | 61 | a0001c0001t0001g0071a0001c0001t0003g0183a0001c0001t0010g0052others(58): Show | 61 | HG00544.hp1 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.318-8073_318-8072d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541875 | |||||
| chr10:102541875
|
A | ATTT | 8 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0027others(5): Show | 8 | HG00597.hp2 HG02074.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.318-8074_318-8072d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541875 | |||||
| chr10:102541875
|
AT | A | 18 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0166others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.318-8072delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541875 | |||||
| chr10:102541875
|
ATT | A | 62 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(59): Show | 62 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.318-8073_318-8072d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102541875 | |||||
| chr10:102541975
|
C | G | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.318-7995C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541975 | ||||||
| chr10:102542139
|
G | GT | 78 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(75): Show | 78 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.318-7820dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102542139 | |||||
| chr10:102542169
|
G | A | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.318-7801G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542169 | ||||||
| chr10:102542370
|
A | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-7600A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542370 | ||||||
| chr10:102542399
|
G | A | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.318-7571G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542399 | ||||||
| chr10:102542423
|
G | T | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.318-7547G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542423 | ||||||
| chr10:102542430
|
C | CTA | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | HG02280.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-7526_318-7525d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102542430 | |||||
| chr10:102542430
|
CTA | C | 70 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(67): Show | 70 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.318-7526_318-7525d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102542430 | |||||
| chr10:102542444
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318-7526A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542444 | ||||||
| chr10:102542444
|
ATT | A | 13 | a0001c0001t0001g0115a0001c0001t0001g0148a0001c0001t0001g0150others(10): Show | 13 | HG01175.hp2 HG01891.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.318-7518_318-7517d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102542444 | |||||
| chr10:102542446
|
T | A | 168 | a0001c0001t0001g0071a0001c0001t0001g0176a0001c0001t0001g0177others(165): Show | 168 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.318-7524T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542446 | ||||||
| chr10:102542448
|
T | A | 1 | a0001c0002t0002g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.318-7522T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542448 | ||||||
| chr10:102542513
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.318-7457G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542513 | ||||||
| chr10:102542530
|
C | T | 1 | a0001c0001t0019g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.318-7440C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542530 | ||||||
| chr10:102542580
|
C | T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-7390C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542580 | ||||||
| chr10:102542626
|
CT | C | 259 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(256): Show | 259 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(256): Show |
intron_variant | MODIFIER | c.318-7328delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102542626 | |||||
| chr10:102542797
|
G | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.318-7173G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542797 | ||||||
| chr10:102542870
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-7100C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542870 | ||||||
| chr10:102542871
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318-7099G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542871 | ||||||
| chr10:102542914
|
C | T | 1 | a0001c0002t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.318-7056C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542914 | ||||||
| chr10:102542936
|
T | C | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-7034T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102542936 | ||||||
| chr10:102543112
|
C | T | 1 | a0001c0002t0002g0006 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.318-6858C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543112 | ||||||
| chr10:102543176
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-6794G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543176 | ||||||
| chr10:102543202
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-6768C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543202 | ||||||
| chr10:102543285
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.318-6685A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543285 | ||||||
| chr10:102543354
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318-6616C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543354 | ||||||
| chr10:102543701
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.318-6269T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543701 | ||||||
| chr10:102543735
|
T | C | 1 | a0001c0001t0012g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318-6235T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543735 | ||||||
| chr10:102543752
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.318-6218C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543752 | ||||||
| chr10:102543991
|
C | T | 54 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(51): Show | 54 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.318-5979C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102543991 | ||||||
| chr10:102544126
|
T | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-5844T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102544126 | ||||||
| chr10:102544316
|
T | C | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.318-5654T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102544316 | ||||||
| chr10:102544569
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.318-5401C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102544569 | ||||||
| chr10:102544910
|
G | A | 56 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(53): Show | 56 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.318-5060G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102544910 | ||||||
| chr10:102544986
|
G | A | 263 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.318-4984G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102544986 | ||||||
| chr10:102545009
|
T | C | 75 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.318-4961T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545009 | ||||||
| chr10:102545022
|
G | C | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.318-4948G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545022 | ||||||
| chr10:102545284
|
A | G | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG02280.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.318-4686A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545284 | ||||||
| chr10:102545293
|
A | AT | 109 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0176others(106): Show | 109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.318-4656dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102545293 | |||||
| chr10:102545293
|
A | ATT | 16 | a0001c0001t0001g0177a0001c0001t0001g0188a0001c0001t0001g0206others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-4657_318-4656d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102545293 | |||||
| chr10:102545293
|
ATT | A | 7 | a0001c0002t0002g0098a0001c0002t0002g0100a0001c0002t0002g0102others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.318-4657_318-4656d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102545293 | |||||
| chr10:102545323
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.318-4647G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545323 | ||||||
| chr10:102545362
|
C | T | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.318-4608C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545362 | ||||||
| chr10:102545428
|
C | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-4542C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545428 | ||||||
| chr10:102545527
|
T | C | 1 | a0001c0004t0003g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318-4443T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545527 | ||||||
| chr10:102545744
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.318-4226C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545744 | ||||||
| chr10:102545900
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.318-4070G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102545900 | ||||||
| chr10:102546039
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.318-3931G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546039 | ||||||
| chr10:102546206
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG02280.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.318-3764G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546206 | ||||||
| chr10:102546403
|
G | T | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-3567G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546403 | ||||||
| chr10:102546926
|
C | T | 4 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(1): Show | 4 | HG01070.hp2 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-3044C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546926 | ||||||
| chr10:102546952
|
C | T | 1 | a0001c0001t0003g0221 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.318-3018C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546952 | ||||||
| chr10:102546963
|
G | A | 1 | a0001c0002t0002g0011 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.318-3007G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102546963 | ||||||
| chr10:102547249
|
A | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.318-2721A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102547249 | ||||||
| chr10:102547430
|
C | G | 1 | a0001c0001t0005g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.318-2540C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102547430 | ||||||
| chr10:102547747
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.318-2223G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102547747 | ||||||
| chr10:102547807
|
G | A | 1 | a0001c0002t0007g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.318-2163G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102547807 | ||||||
| chr10:102547832
|
G | A | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.318-2138G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102547832 | ||||||
| chr10:102547832
|
G | GGAGAGAG others(7): Show |
1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318-2137_318-2124d others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 102547832 | |||||
| chr10:102548026
|
A | G | 1 | a0001c0002t0007g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.318-1944A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548026 | ||||||
| chr10:102548198
|
G | C | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-1772G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548198 | ||||||
| chr10:102548202
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG00280.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.318-1768C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548202 | ||||||
| chr10:102548303
|
G | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-1667G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548303 | ||||||
| chr10:102548307
|
T | G | 83 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(80): Show | 83 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.318-1663T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548307 | ||||||
| chr10:102548316
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.318-1654A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548316 | ||||||
| chr10:102548436
|
T | C | 110 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(107): Show | 110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.318-1534T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548436 | ||||||
| chr10:102548689
|
C | T | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.318-1281C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102548689 | ||||||
| chr10:102549074
|
G | A | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.318-896G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102549074 | ||||||
| chr10:102549438
|
G | A | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318-532G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102549438 | ||||||
| chr10:102549814
|
G | T | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.318-156G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102549814 | ||||||
| chr10:102550430
|
C | A | 1 | a0001c0001t0012g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.454+324C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102550430 | ||||||
| chr10:102550473
|
G | A | 1 | a0001c0002t0002g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.454+367G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102550473 | ||||||
| chr10:102550742
|
C | CT | 58 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(55): Show | 58 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.454+652dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102550742 | |||||
| chr10:102550742
|
C | CTT | 47 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(44): Show | 47 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.454+651_454+652dup others(2): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102550742 | |||||
| chr10:102550742
|
C | CTTT | 9 | a0001c0001t0001g0186a0001c0001t0005g0073a0001c0001t0005g0080others(6): Show | 9 | HG01074.hp1 HG01081.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+650_454+652dup others(3): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102550742 | |||||
| chr10:102550742
|
CT | C | 85 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(82): Show | 85 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.454+652delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102550742 | |||||
| chr10:102551008
|
G | C | 1 | a0001c0001t0012g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.454+902G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102551008 | ||||||
| chr10:102551133
|
C | A | 1 | a0001c0001t0031g0258 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.454+1027C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102551133 | ||||||
| chr10:102551168
|
C | T | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+1062C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102551168 | ||||||
| chr10:102551298
|
G | A | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.454+1192G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102551298 | ||||||
| chr10:102551717
|
C | CT | 74 | a0001c0001t0001g0071a0001c0001t0001g0143a0001c0001t0001g0169others(71): Show | 74 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.454+1635dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102551717 | |||||
| chr10:102551717
|
C | CTT | 7 | a0001c0002t0002g0007a0001c0002t0002g0015a0001c0002t0002g0019others(4): Show | 7 | HG01978.hp1 HG02074.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+1634_454+1635d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102551717 | |||||
| chr10:102551717
|
CT | C | 9 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0005g0080others(6): Show | 9 | HG01074.hp1 HG01943.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+1635delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102551717 | |||||
| chr10:102551717
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.454+1621_454+1635d others(17): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102551717 | |||||
| chr10:102551859
|
C | G | 1 | a0001c0002t0002g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.454+1753C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102551859 | ||||||
| chr10:102552144
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.454+2038C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552144 | ||||||
| chr10:102552290
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.454+2184C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552290 | ||||||
| chr10:102552329
|
AG | A | 17 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0006g0216others(14): Show | 17 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.454+2225delG | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102552329 | |||||
| chr10:102552459
|
G | A | 2 | a0001c0002t0002g0026a0001c0002t0002g0043 | 2 | HG02809.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.454+2353G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552459 | ||||||
| chr10:102552503
|
C | T | 1 | a0001c0002t0002g0045 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.454+2397C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552503 | ||||||
| chr10:102552662
|
T | G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0123others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+2556T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552662 | ||||||
| chr10:102552728
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.454+2622C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102552728 | ||||||
| chr10:102552784
|
CTTAA | C | 3 | a0001c0001t0010g0052a0001c0002t0026g0036a0001c0002t0029g0037 | 3 | HG02615.hp2 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.454+2681_454+2684d others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102552784 | |||||
| chr10:102553205
|
A | G | 2 | a0001c0002t0002g0011a0001c0002t0002g0028 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.454+3099A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553205 | ||||||
| chr10:102553342
|
T | C | 1 | a0001c0001t0019g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.454+3236T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553342 | ||||||
| chr10:102553464
|
AT | A | 10 | a0001c0001t0001g0123a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+3375delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102553464 | |||||
| chr10:102553608
|
C | T | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.454+3502C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553608 | ||||||
| chr10:102553620
|
C | T | 47 | a0001c0001t0001g0161a0001c0001t0001g0232a0001c0001t0003g0031others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.454+3514C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553620 | ||||||
| chr10:102553638
|
C | T | 149 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(146): Show | 149 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(146): Show |
intron_variant | MODIFIER | c.454+3532C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553638 | ||||||
| chr10:102553656
|
G | C | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.454+3550G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553656 | ||||||
| chr10:102553677
|
A | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0009g0189others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+3571A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553677 | ||||||
| chr10:102553770
|
CA | C | 67 | a0001c0001t0001g0071a0001c0001t0010g0052a0001c0002t0002g0001others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.454+3667delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102553770 | |||||
| chr10:102553991
|
G | A | 1 | a0001c0001t0006g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+3885G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102553991 | ||||||
| chr10:102554009
|
C | T | 6 | a0001c0002t0002g0019a0001c0002t0002g0048a0001c0002t0002g0051others(3): Show | 6 | NA18957.hp1 NA18965.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+3903C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554009 | ||||||
| chr10:102554065
|
A | T | 1 | a0001c0001t0006g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.454+3959A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554065 | ||||||
| chr10:102554254
|
T | A | 13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+4148T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554254 | ||||||
| chr10:102554296
|
G | A | 1 | a0001c0002t0002g0034 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.454+4190G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554296 | ||||||
| chr10:102554466
|
A | G | 1 | a0001c0001t0006g0255 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.454+4360A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554466 | ||||||
| chr10:102554663
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.454+4557G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554663 | ||||||
| chr10:102554874
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.454+4768G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554874 | ||||||
| chr10:102554949
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.454+4843A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554949 | ||||||
| chr10:102554949
|
A | G | 1 | a0001c0001t0005g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.454+4843A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554949 | ||||||
| chr10:102554997
|
A | G | 1 | a0001c0002t0002g0045 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.454+4891A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102554997 | ||||||
| chr10:102555006
|
T | C | 1 | a0001c0001t0005g0078 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.454+4900T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555006 | ||||||
| chr10:102555034
|
C | T | 1 | a0001c0002t0030g0089 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.454+4928C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555034 | ||||||
| chr10:102555065
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.454+4959A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555065 | ||||||
| chr10:102555112
|
A | C | 4 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0146others(1): Show | 4 | NA18944.hp2 NA18979.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+5006A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555112 | ||||||
| chr10:102555124
|
C | T | 50 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.454+5018C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555124 | ||||||
| chr10:102555147
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.454+5041G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555147 | ||||||
| chr10:102555269
|
CA | C | 107 | a0001c0001t0001g0111a0001c0001t0001g0132a0001c0001t0001g0142others(104): Show | 107 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.454+5184delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102555269 | |||||
| chr10:102555269
|
CAA | C | 129 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0112others(126): Show | 129 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.454+5183_454+5184d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102555269 | |||||
| chr10:102555321
|
C | CT | 8 | a0001c0001t0001g0139a0001c0001t0001g0155a0001c0001t0001g0186others(5): Show | 8 | HG01978.hp2 HG02074.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+5231dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102555321 | |||||
| chr10:102555391
|
C | T | 1 | a0001c0002t0002g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.454+5285C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555391 | ||||||
| chr10:102555458
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.454+5352G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555458 | ||||||
| chr10:102555910
|
G | A | 58 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(55): Show | 58 | HG00733.hp1 HG01099.hp1 HG01175.hp2 others(55): Show |
intron_variant | MODIFIER | c.454+5804G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102555910 | ||||||
| chr10:102556173
|
C | T | 1 | a0001c0001t0010g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.454+6067C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556173 | ||||||
| chr10:102556179
|
C | T | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.454+6073C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556179 | ||||||
| chr10:102556220
|
CT | C | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.454+6116delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102556220 | |||||
| chr10:102556569
|
C | T | 1 | a0001c0001t0006g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.454+6463C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556569 | ||||||
| chr10:102556570
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.454+6464G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556570 | ||||||
| chr10:102556698
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.454+6592G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556698 | ||||||
| chr10:102556749
|
A | AAAAGGAA others(7): Show |
1 | a0001c0002t0002g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.454+6644_454+6645i others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102556749 | |||||
| chr10:102556749
|
A | AAAGGAAG others(6): Show |
75 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(72): Show | 75 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.454+6644_454+6645i others(15): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102556749 | |||||
| chr10:102556749
|
A | AGGAAGGG others(4): Show |
1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.454+6643_454+6644i others(13): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556749 | ||||||
| chr10:102556757
|
G | A | 77 | a0001c0001t0001g0071a0001c0001t0001g0168a0001c0002t0002g0001others(74): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.454+6651G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556757 | ||||||
| chr10:102556757
|
G | GAGGGAGG others(5): Show |
74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.454+6657_454+6668d others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102556757 | |||||
| chr10:102556824
|
C | A | 48 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(45): Show | 48 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.454+6718C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556824 | ||||||
| chr10:102556855
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.454+6749C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556855 | ||||||
| chr10:102557435
|
T | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+7329T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102557435 | ||||||
| chr10:102557479
|
G | C | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.454+7373G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102557479 | ||||||
| chr10:102557508
|
ACTTGAGC others(18): Show |
A | 1 | a0001c0002t0002g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.454+7428_454+7452d others(27): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102557508 | |||||
| chr10:102557600
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+7494G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102557600 | ||||||
| chr10:102557881
|
C | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+7775C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102557881 | ||||||
| chr10:102558028
|
T | G | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.454+7922T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558028 | ||||||
| chr10:102558051
|
C | CA | 53 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.454+7947dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102558051 | |||||
| chr10:102558054
|
C | A | 53 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.454+7948C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558054 | ||||||
| chr10:102558259
|
A | T | 1 | a0001c0001t0004g0130 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.454+8153A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558259 | ||||||
| chr10:102558565
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+8459G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558565 | ||||||
| chr10:102558586
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.454+8480A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558586 | ||||||
| chr10:102558951
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.454+8845A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102558951 | ||||||
| chr10:102559122
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG03017.hp1 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.454+9016C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102559122 | ||||||
| chr10:102559209
|
A | G | 133 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(130): Show | 133 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.454+9103A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102559209 | ||||||
| chr10:102559370
|
TC | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+9268delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102559370 | |||||
| chr10:102559468
|
C | T | 1 | a0001c0002t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.454+9362C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102559468 | ||||||
| chr10:102559627
|
C | T | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.454+9521C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102559627 | ||||||
| chr10:102560050
|
G | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.454+9944G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560050 | ||||||
| chr10:102560190
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.454+10084G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560190 | ||||||
| chr10:102560272
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+10166G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560272 | ||||||
| chr10:102560591
|
C | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+10485C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560591 | ||||||
| chr10:102560691
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0147 | 2 | NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.454+10585C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560691 | ||||||
| chr10:102560712
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+10606A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560712 | ||||||
| chr10:102560719
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+10613G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560719 | ||||||
| chr10:102560906
|
C | T | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.454+10800C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560906 | ||||||
| chr10:102560911
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+10805C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102560911 | ||||||
| chr10:102561031
|
C | T | 15 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(12): Show | 15 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.454+10925C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561031 | ||||||
| chr10:102561085
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0075 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.454+10979C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561085 | ||||||
| chr10:102561136
|
C | T | 1 | a0001c0001t0008g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.454+11030C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561136 | ||||||
| chr10:102561141
|
C | G | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.454+11035C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561141 | ||||||
| chr10:102561376
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.454+11270T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561376 | ||||||
| chr10:102561667
|
C | CT | 87 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0001g0113others(84): Show | 87 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.454+11580dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102561667 | |||||
| chr10:102561667
|
C | CTT | 78 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(75): Show | 78 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.454+11579_454+1158 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102561667 | |||||
| chr10:102561667
|
C | CTTT | 5 | a0001c0001t0001g0132a0001c0001t0001g0162a0001c0001t0001g0166others(2): Show | 5 | HG01261.hp2 HG01358.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+11578_454+1158 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102561667 | |||||
| chr10:102561667
|
CT | C | 45 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(42): Show | 45 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.454+11580delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102561667 | |||||
| chr10:102561809
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454+11703C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561809 | ||||||
| chr10:102561964
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.454+11858T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102561964 | ||||||
| chr10:102563271
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+13165G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563271 | ||||||
| chr10:102563346
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+13240G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563346 | ||||||
| chr10:102563608
|
GCTGCAGT others(17): Show |
G | 3 | a0001c0001t0004g0114a0001c0001t0004g0119a0001c0001t0004g0120 | 3 | HG02074.hp1 NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.454+13532_454+1355 others(28): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102563608 | |||||
| chr10:102563782
|
G | T | 265 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(262): Show | 265 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(262): Show |
intron_variant | MODIFIER | c.454+13676G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563782 | ||||||
| chr10:102563801
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.454+13695C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563801 | ||||||
| chr10:102563880
|
G | A | 2 | a0001c0002t0026g0036a0001c0002t0029g0037 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.454+13774G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563880 | ||||||
| chr10:102563978
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.454+13872A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102563978 | ||||||
| chr10:102564276
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.454+14170C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102564276 | ||||||
| chr10:102564478
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.454+14372G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102564478 | ||||||
| chr10:102564500
|
T | A | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.454+14394T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102564500 | ||||||
| chr10:102564617
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.454+14511G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102564617 | ||||||
| chr10:102564853
|
G | A | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.454+14747G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102564853 | ||||||
| chr10:102565149
|
T | G | 15 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(12): Show | 15 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.454+15043T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102565149 | ||||||
| chr10:102565384
|
A | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454+15278A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102565384 | ||||||
| chr10:102565832
|
C | T | 1 | a0001c0001t0015g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.454+15726C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102565832 | ||||||
| chr10:102566139
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+16033A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566139 | ||||||
| chr10:102566185
|
G | A | 3 | a0001c0002t0002g0012a0001c0002t0002g0013a0001c0002t0002g0014 | 3 | HG00639.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.454+16079G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566185 | ||||||
| chr10:102566200
|
G | A | 21 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(18): Show | 21 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.454+16094G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566200 | ||||||
| chr10:102566227
|
C | G | 2 | a0001c0002t0002g0035a0001c0002t0002g0039 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.454+16121C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566227 | ||||||
| chr10:102566679
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.454+16573C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566679 | ||||||
| chr10:102566764
|
C | CA | 11 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0213others(8): Show | 11 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+16678dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102566764 | |||||
| chr10:102566764
|
CAA | C | 138 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(135): Show | 138 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.454+16677_454+1667 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102566764 | |||||
| chr10:102566764
|
CAAA | C | 9 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+16676_454+1667 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102566764 | |||||
| chr10:102566825
|
G | T | 2 | a0001c0001t0009g0189a0001c0001t0009g0192 | 2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.454+16719G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566825 | ||||||
| chr10:102566876
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454+16770C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102566876 | ||||||
| chr10:102566942
|
C | CA | 6 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0001g0141others(3): Show | 6 | HG01175.hp2 HG01255.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+16849dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102566942 | |||||
| chr10:102567006
|
C | CTT | 102 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.454+16922_454+1692 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102567006 | |||||
| chr10:102567006
|
C | CTTT | 123 | a0001c0001t0001g0071a0001c0001t0001g0115a0001c0001t0001g0116others(120): Show | 123 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.454+16921_454+1692 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102567006 | |||||
| chr10:102567006
|
C | CTTTT | 31 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0187others(28): Show | 31 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.454+16920_454+1692 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102567006 | |||||
| chr10:102567050
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.454+16944T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567050 | ||||||
| chr10:102567088
|
T | G | 1 | a0001c0002t0002g0011 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.454+16982T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567088 | ||||||
| chr10:102567407
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.454+17301A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567407 | ||||||
| chr10:102567445
|
C | T | 3 | a0001c0001t0010g0052a0001c0001t0010g0137a0001c0001t0034g0076 | 3 | HG02717.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.454+17339C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567445 | ||||||
| chr10:102567612
|
C | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.454+17506C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567612 | ||||||
| chr10:102567639
|
G | T | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.454+17533G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567639 | ||||||
| chr10:102567751
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.454+17645T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567751 | ||||||
| chr10:102567827
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.454+17721A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567827 | ||||||
| chr10:102567947
|
G | C | 1 | a0001c0002t0007g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.454+17841G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102567947 | ||||||
| chr10:102568093
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0135 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.454+17987A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568093 | ||||||
| chr10:102568108
|
TC | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+18005delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568108 | |||||
| chr10:102568145
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+18039A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568145 | ||||||
| chr10:102568146
|
A | G | 1 | a0001c0002t0002g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.454+18040A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568146 | ||||||
| chr10:102568209
|
T | TA | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.454+18117dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568209 | |||||
| chr10:102568358
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.454+18252G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568358 | ||||||
| chr10:102568509
|
G | T | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.454+18403G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568509 | ||||||
| chr10:102568611
|
C | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+18505C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568611 | ||||||
| chr10:102568616
|
G | A | 1 | a0001c0004t0003g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.454+18510G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568616 | ||||||
| chr10:102568874
|
C | CAA | 12 | a0001c0001t0001g0194a0001c0001t0001g0232a0001c0001t0001g0242others(9): Show | 12 | HG00642.hp1 HG00733.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+18791_454+1879 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
C | CAAA | 9 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0195others(6): Show | 9 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+18790_454+1879 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
C | CAAAA | 6 | a0001c0001t0001g0185a0001c0001t0001g0193a0001c0001t0001g0203others(3): Show | 6 | HG00741.hp1 HG01169.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+18789_454+1879 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
C | CAAAAA | 11 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0197others(8): Show | 11 | HG01074.hp2 HG01258.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+18788_454+1879 others(9): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.454+18783_454+1879 others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
CA | C | 26 | a0001c0001t0003g0228a0001c0001t0003g0238a0001c0001t0003g0250others(23): Show | 26 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.454+18792delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568874
|
CAA | C | 6 | a0001c0001t0015g0231a0001c0002t0002g0029a0001c0002t0002g0038others(3): Show | 6 | HG02897.hp2 HG03017.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+18791_454+1879 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568874 | |||||
| chr10:102568889
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0155 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.454+18785_454+1880 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568889 | |||||
| chr10:102568890
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.454+18786_454+1880 others(21): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568890 | |||||
| chr10:102568890
|
AAAAAAAA others(12): Show |
A | 5 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0170others(2): Show | 5 | HG02040.hp1 HG02717.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+18786_454+1880 others(23): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568890 | |||||
| chr10:102568891
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.454+18787_454+1880 others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568891 | |||||
| chr10:102568891
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454+18787_454+1880 others(20): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568891 | |||||
| chr10:102568891
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0139a0001c0001t0001g0171 | 2 | NA18979.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.454+18787_454+1880 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568891 | |||||
| chr10:102568891
|
AAAAAAAA others(17): Show |
A | 3 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0136 | 3 | HG01069.hp1 HG01071.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.454+18787_454+1881 others(28): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568891 | |||||
| chr10:102568891
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.454+18787_454+1881 others(30): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568891 | |||||
| chr10:102568892
|
AAAAAAAT others(10): Show |
A | 10 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0166others(7): Show | 10 | HG01358.hp1 HG01928.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.454+18788_454+1880 others(21): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568892 | |||||
| chr10:102568892
|
AAAAAAAT others(12): Show |
A | 16 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0001g0140others(13): Show | 16 | HG01099.hp1 HG01175.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.454+18788_454+1880 others(23): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568892 | |||||
| chr10:102568892
|
AAAAAAAT others(44): Show |
A | 2 | a0001c0001t0001g0154a0001c0001t0021g0153 | 2 | HG00733.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.454+18788_454+1883 others(55): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568892 | |||||
| chr10:102568893
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.454+18787A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568893 | ||||||
| chr10:102568893
|
AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.454+18789_454+1880 others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568893 | |||||
| chr10:102568893
|
AAAAAATA others(7): Show |
A | 1 | a0001c0002t0002g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.454+18789_454+1880 others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568893 | |||||
| chr10:102568893
|
AAAAAATA others(9): Show |
A | 2 | a0001c0002t0002g0098a0001c0002t0002g0101 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.454+18789_454+1880 others(20): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568893 | |||||
| chr10:102568893
|
AAAAAATA others(11): Show |
A | 7 | a0001c0001t0001g0111a0001c0001t0001g0144a0001c0001t0004g0107others(4): Show | 7 | HG02027.hp2 HG03831.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+18789_454+1880 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568893 | |||||
| chr10:102568894
|
AAAAATAT others(8): Show |
A | 1 | a0001c0002t0002g0100 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454+18790_454+1880 others(19): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568894 | |||||
| chr10:102568894
|
AAAAATAT others(10): Show |
A | 10 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0124others(7): Show | 10 | HG02071.hp1 HG02717.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.454+18790_454+1880 others(21): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568894 | |||||
| chr10:102568894
|
AAAAATAT others(12): Show |
A | 6 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0150others(3): Show | 6 | HG00280.hp1 HG01261.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+18790_454+1880 others(23): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568894 | |||||
| chr10:102568895
|
A | AT | 11 | a0001c0001t0001g0212a0001c0001t0001g0247a0001c0002t0002g0009others(8): Show | 11 | HG01978.hp1 HG03041.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.454+18789_454+1879 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568895 | ||||||
| chr10:102568895
|
A | T | 11 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0148others(8): Show | 11 | HG01255.hp2 HG02129.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.454+18789A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568895 | ||||||
| chr10:102568896
|
AAATATAT others(4): Show |
A | 1 | a0001c0001t0008g0022 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.454+18792_454+1880 others(15): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568896 | |||||
| chr10:102568896
|
AAATATAT others(8): Show |
A | 1 | a0001c0002t0007g0103 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.454+18792_454+1880 others(19): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568896 | |||||
| chr10:102568897
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0013g0249 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.454+18792_454+1879 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568897 | |||||
| chr10:102568897
|
A | AT | 13 | a0001c0001t0001g0149a0001c0001t0003g0221a0001c0001t0003g0227others(10): Show | 13 | HG00558.hp2 HG01081.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+18791_454+1879 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568897 | ||||||
| chr10:102568897
|
A | T | 63 | a0001c0001t0001g0071a0001c0001t0001g0118a0001c0001t0001g0123others(60): Show | 63 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.454+18791A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568897 | ||||||
| chr10:102568898
|
AT | A | 5 | a0001c0001t0001g0214a0001c0001t0011g0067a0001c0001t0014g0018others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+18793delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568898 | ||||||
| chr10:102568898
|
ATATATAT others(8): Show |
A | 1 | a0001c0002t0007g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.454+18793_454+1880 others(19): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568898 | ||||||
| chr10:102568899
|
T | A | 46 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0185others(43): Show | 46 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.454+18793T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568899 | ||||||
| chr10:102568901
|
T | A | 24 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0196others(21): Show | 24 | HG00639.hp1 HG01074.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.454+18795T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568901 | ||||||
| chr10:102568901
|
TATATATA others(15): Show |
T | 8 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130others(5): Show | 8 | HG02922.hp2 NA18952.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+18815_454+1883 others(26): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568901 | |||||
| chr10:102568903
|
T | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0259others(8): Show | 11 | HG01169.hp2 HG01258.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.454+18797T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568903 | ||||||
| chr10:102568903
|
TATATATA others(13): Show |
T | 1 | a0001c0002t0007g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454+18815_454+1883 others(24): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568903 | |||||
| chr10:102568905
|
T | A | 2 | a0001c0001t0014g0018a0001c0001t0017g0200 | 2 | HG01952.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.454+18799T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568905 | ||||||
| chr10:102568905
|
TATATATA others(11): Show |
T | 1 | a0001c0002t0007g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.454+18815_454+1883 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568905 | |||||
| chr10:102568907
|
TATATATA others(9): Show |
T | 1 | a0001c0002t0007g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.454+18815_454+1883 others(20): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568907 | |||||
| chr10:102568911
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.454+18815_454+1882 others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568911 | |||||
| chr10:102568919
|
TACAC | T | 74 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(71): Show | 74 | HG00280.hp1 HG01099.hp1 HG01175.hp2 others(71): Show |
intron_variant | MODIFIER | c.454+18815_454+1881 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568919 | |||||
| chr10:102568921
|
C | T | 108 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0136others(105): Show | 108 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.454+18815C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568921 | ||||||
| chr10:102568921
|
CACATATA others(15): Show |
C | 3 | a0001c0001t0001g0123a0001c0001t0004g0119a0001c0001t0004g0120 | 3 | HG03041.hp2 NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.454+18817_454+1883 others(26): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568921 | |||||
| chr10:102568921
|
CACATATA others(17): Show |
C | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0152others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+18817_454+1884 others(28): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568921 | |||||
| chr10:102568923
|
C | T | 112 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0134others(109): Show | 112 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.454+18817C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568923 | ||||||
| chr10:102568923
|
CATATATA others(15): Show |
C | 2 | a0001c0002t0002g0011a0001c0002t0002g0028 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.454+18836_454+1885 others(26): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568923 | |||||
| chr10:102568923
|
CATATATA others(17): Show |
C | 44 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(41): Show | 44 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.454+18834_454+1885 others(28): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568923 | |||||
| chr10:102568923
|
CATATATA others(19): Show |
C | 6 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0034others(3): Show | 6 | HG02273.hp1 HG02300.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+18832_454+1885 others(30): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568923 | |||||
| chr10:102568931
|
T | C | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+18825T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568931 | ||||||
| chr10:102568933
|
T | C | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01099.hp2 HG01928.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+18827T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568933 | ||||||
| chr10:102568933
|
T | TAC | 3 | a0001c0001t0001g0246a0001c0001t0003g0265a0001c0001t0003g0266 | 3 | HG01070.hp2 HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.454+18828_454+1882 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568933 | |||||
| chr10:102568935
|
T | C | 38 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0202others(35): Show | 38 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.454+18829T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568935 | ||||||
| chr10:102568935
|
T | TAC | 4 | a0001c0001t0003g0183a0001c0001t0003g0217a0001c0001t0031g0258others(1): Show | 4 | HG00741.hp2 HG01192.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+18830_454+1883 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568935 | |||||
| chr10:102568937
|
T | C | 72 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(69): Show | 72 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.454+18831T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568937 | ||||||
| chr10:102568937
|
T | TACAC | 7 | a0001c0001t0001g0213a0001c0001t0003g0239a0001c0001t0006g0216others(4): Show | 7 | HG00597.hp1 HG02056.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+18832_454+1883 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568937 | |||||
| chr10:102568937
|
T | TATATATA others(5): Show |
1 | a0001c0001t0012g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.454+18840_454+1884 others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568937 | |||||
| chr10:102568939
|
T | C | 47 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(44): Show | 47 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.454+18833T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568939 | ||||||
| chr10:102568939
|
T | TATATATA others(3): Show |
4 | a0001c0001t0005g0078a0001c0001t0005g0080a0001c0001t0005g0081others(1): Show | 4 | HG01074.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+18840_454+1884 others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568939 | |||||
| chr10:102568940
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454+18834A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568940 | ||||||
| chr10:102568941
|
T | C | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+18835T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568941 | ||||||
| chr10:102568943
|
T | C | 8 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0124others(5): Show | 8 | HG01358.hp1 HG02074.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+18837T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568943 | ||||||
| chr10:102568945
|
T | C | 64 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(61): Show | 64 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.454+18839T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568945 | ||||||
| chr10:102568947
|
T | C | 22 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(19): Show | 22 | HG01891.hp1 HG02071.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.454+18841T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568947 | ||||||
| chr10:102568947
|
T | TACAC | 4 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0060others(1): Show | 4 | NA18959.hp2 NA18962.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+18842_454+1884 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102568947 | |||||
| chr10:102568954
|
A | C | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.454+18848A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568954 | ||||||
| chr10:102568958
|
A | C | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.454+18852A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568958 | ||||||
| chr10:102568962
|
A | C | 109 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(106): Show | 109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.454+18856A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102568962 | ||||||
| chr10:102569102
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.454+18996G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569102 | ||||||
| chr10:102569138
|
A | G | 3 | a0001c0002t0002g0012a0001c0002t0002g0013a0001c0002t0002g0014 | 3 | HG00639.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.454+19032A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569138 | ||||||
| chr10:102569345
|
G | A | 2 | a0001c0002t0026g0036a0001c0002t0029g0037 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.454+19239G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569345 | ||||||
| chr10:102569405
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0136 | 2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.454+19299C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569405 | ||||||
| chr10:102569864
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+19758G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569864 | ||||||
| chr10:102569884
|
A | G | 1 | a0001c0002t0002g0004 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.454+19778A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569884 | ||||||
| chr10:102569913
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.454+19807C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569913 | ||||||
| chr10:102569928
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.454+19822A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102569928 | ||||||
| chr10:102570231
|
ATATT | A | 260 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(257): Show | 260 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(257): Show |
intron_variant | MODIFIER | c.454+20150_454+2015 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102570231 | |||||
| chr10:102570320
|
C | T | 108 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(105): Show | 108 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.454+20214C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102570320 | ||||||
| chr10:102570430
|
A | G | 2 | a0001c0001t0012g0236a0001c0001t0012g0262 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.454+20324A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102570430 | ||||||
| chr10:102570539
|
T | TTTTG | 154 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(151): Show | 154 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.454+20445_454+2044 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102570539 | |||||
| chr10:102570807
|
G | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.454+20701G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102570807 | ||||||
| chr10:102570995
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.454+20889A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102570995 | ||||||
| chr10:102571046
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.454+20940G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571046 | ||||||
| chr10:102571121
|
T | A | 9 | a0001c0001t0001g0232a0001c0001t0003g0217a0001c0001t0003g0223others(6): Show | 9 | HG00733.hp2 HG01070.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+21015T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571121 | ||||||
| chr10:102571233
|
A | G | 19 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0132others(16): Show | 19 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.454+21127A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571233 | ||||||
| chr10:102571386
|
C | T | 1 | a0001c0001t0033g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.455-21196C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571386 | ||||||
| chr10:102571505
|
A | AAAAC | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.455-21065_455-2106 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102571505 | |||||
| chr10:102571576
|
G | C | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.455-21006G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571576 | ||||||
| chr10:102571590
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.455-20992T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571590 | ||||||
| chr10:102571700
|
A | G | 13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.455-20882A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571700 | ||||||
| chr10:102571724
|
A | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.455-20858A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571724 | ||||||
| chr10:102571858
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.455-20724A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571858 | ||||||
| chr10:102571902
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.455-20680T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571902 | ||||||
| chr10:102572001
|
C | T | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.455-20581C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102572001 | ||||||
| chr10:102572190
|
C | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.455-20392C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102572190 | ||||||
| chr10:102572229
|
A | G | 154 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(151): Show | 154 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.455-20353A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102572229 | ||||||
| chr10:102572232
|
AT | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.455-20335delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102572232 | |||||
| chr10:102572248
|
G | T | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.455-20334G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102572248 | ||||||
| chr10:102572392
|
C | CT | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.455-20175dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102572392 | |||||
| chr10:102572494
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-20088A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102572494 | ||||||
| chr10:102573026
|
C | G | 1 | a0001c0001t0008g0022 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455-19556C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573026 | ||||||
| chr10:102573083
|
C | T | 5 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-19499C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573083 | ||||||
| chr10:102573198
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.455-19384G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573198 | ||||||
| chr10:102573482
|
G | A | 2 | a0001c0001t0006g0255a0001c0001t0006g0256 | 2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.455-19100G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573482 | ||||||
| chr10:102573707
|
G | A | 12 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0073others(9): Show | 12 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.455-18875G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573707 | ||||||
| chr10:102573943
|
C | T | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-18639C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102573943 | ||||||
| chr10:102574050
|
A | G | 1 | a0001c0002t0002g0061 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.455-18532A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574050 | ||||||
| chr10:102574137
|
G | T | 1 | a0001c0002t0030g0089 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.455-18445G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574137 | ||||||
| chr10:102574386
|
G | A | 1 | a0001c0002t0002g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.455-18196G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574386 | ||||||
| chr10:102574524
|
G | T | 1 | a0001c0002t0002g0055 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.455-18058G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574524 | ||||||
| chr10:102574562
|
G | A | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.455-18020G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574562 | ||||||
| chr10:102574587
|
T | G | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.455-17995T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574587 | ||||||
| chr10:102574832
|
G | A | 76 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(73): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.455-17750G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574832 | ||||||
| chr10:102574888
|
G | A | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-17694G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102574888 | ||||||
| chr10:102575055
|
C | CA | 12 | a0001c0001t0001g0138a0001c0001t0001g0147a0001c0001t0001g0195others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-17512dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102575055 | |||||
| chr10:102575065
|
A | C | 62 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(59): Show | 62 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.455-17517A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575065 | ||||||
| chr10:102575117
|
G | C | 76 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(73): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.455-17465G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575117 | ||||||
| chr10:102575217
|
A | T | 1 | a0001c0001t0009g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.455-17365A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575217 | ||||||
| chr10:102575340
|
A | G | 1 | a0001c0001t0015g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.455-17242A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575340 | ||||||
| chr10:102575572
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0123 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.455-17010A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575572 | ||||||
| chr10:102575848
|
G | T | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.455-16734G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575848 | ||||||
| chr10:102575899
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-16683G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102575899 | ||||||
| chr10:102576013
|
GT | G | 148 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(145): Show | 148 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.455-16556delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102576013 | |||||
| chr10:102576335
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.455-16247T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102576335 | ||||||
| chr10:102576669
|
A | C | 31 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(28): Show | 31 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.455-15913A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102576669 | ||||||
| chr10:102576881
|
T | C | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-15701T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102576881 | ||||||
| chr10:102577057
|
T | C | 1 | a0001c0001t0003g0250 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.455-15525T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577057 | ||||||
| chr10:102577080
|
C | CT | 125 | a0001c0001t0001g0071a0001c0001t0001g0176a0001c0001t0001g0177others(122): Show | 125 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.455-15498dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102577080 | |||||
| chr10:102577080
|
C | CTT | 3 | a0001c0002t0002g0001a0001c0002t0002g0042a0001c0002t0002g0049 | 3 | HG00597.hp2 HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.455-15499_455-1549 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102577080 | |||||
| chr10:102577080
|
CTTTTCTT others(3): Show |
C | 7 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(4): Show | 7 | NA18941.hp1 NA18943.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-15497_455-1548 others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102577080 | |||||
| chr10:102577085
|
C | T | 255 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(252): Show | 255 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(252): Show |
intron_variant | MODIFIER | c.455-15497C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577085 | ||||||
| chr10:102577086
|
T | TC | 75 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-15496_455-1549 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577086 | ||||||
| chr10:102577229
|
G | A | 110 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(107): Show | 110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.455-15353G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577229 | ||||||
| chr10:102577237
|
A | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-15345A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577237 | ||||||
| chr10:102577240
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-15342C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577240 | ||||||
| chr10:102577682
|
GT | G | 148 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(145): Show | 148 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.455-14884delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102577682 | |||||
| chr10:102577705
|
T | G | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.455-14877T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577705 | ||||||
| chr10:102577762
|
G | C | 1 | a0001c0001t0006g0257 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.455-14820G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577762 | ||||||
| chr10:102577767
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-14815G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577767 | ||||||
| chr10:102577775
|
G | A | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.455-14807G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102577775 | ||||||
| chr10:102578181
|
G | A | 48 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(45): Show | 48 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.455-14401G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578181 | ||||||
| chr10:102578188
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-14394A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578188 | ||||||
| chr10:102578208
|
C | T | 2 | a0001c0001t0005g0081a0001c0001t0005g0091 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.455-14374C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578208 | ||||||
| chr10:102578257
|
A | C | 111 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.455-14325A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578257 | ||||||
| chr10:102578320
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-14262G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578320 | ||||||
| chr10:102578380
|
C | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0239a0001c0001t0023g0180 | 3 | HG02602.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.455-14202C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578380 | ||||||
| chr10:102578495
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.455-14087G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578495 | ||||||
| chr10:102578613
|
C | G | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.455-13969C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578613 | ||||||
| chr10:102578632
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-13950T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578632 | ||||||
| chr10:102578706
|
C | CA | 150 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(147): Show | 150 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.455-13861dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102578706 | |||||
| chr10:102578732
|
A | G | 8 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.455-13850A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578732 | ||||||
| chr10:102578856
|
G | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.455-13726G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102578856 | ||||||
| chr10:102578878
|
GA | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-13692delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102578878 | |||||
| chr10:102579006
|
G | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-13576G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579006 | ||||||
| chr10:102579075
|
A | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.455-13507A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579075 | ||||||
| chr10:102579216
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.455-13366G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579216 | ||||||
| chr10:102579239
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0009g0189others(1): Show | 4 | HG00642.hp1 HG00741.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-13343T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579239 | ||||||
| chr10:102579332
|
G | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-13250G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579332 | ||||||
| chr10:102579372
|
C | T | 1 | a0001c0002t0007g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-13210C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102579372 | ||||||
| chr10:102580029
|
A | ACC | 24 | a0001c0001t0001g0213a0001c0001t0001g0247a0001c0001t0003g0181others(21): Show | 24 | HG00558.hp2 HG01070.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.455-12544_455-1254 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCC | 24 | a0001c0001t0001g0215a0001c0001t0001g0232a0001c0001t0001g0246others(21): Show | 24 | HG00280.hp2 HG00544.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.455-12545_455-1254 others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCCC | 20 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(17): Show | 20 | HG00597.hp1 HG00735.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.455-12546_455-1254 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCCCC | 18 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0196others(15): Show | 18 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.455-12547_455-1254 others(9): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCCCCC | 12 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0184others(9): Show | 12 | HG00735.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-12548_455-1254 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCCCCCC others(3): Show |
1 | a0001c0001t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.455-12552_455-1254 others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580029
|
A | ACCCCCCC others(4): Show |
1 | a0001c0001t0001g0260 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.455-12543_455-1254 others(15): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102580029 | |||||
| chr10:102580031
|
C | CA | 66 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.455-12551_455-1255 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580031 | ||||||
| chr10:102580035
|
C | CG | 84 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0113others(81): Show | 84 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.455-12547_455-1254 others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580035 | ||||||
| chr10:102580035
|
C | G | 66 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(63): Show | 66 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.455-12547C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580035 | ||||||
| chr10:102580094
|
T | C | 111 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.455-12488T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580094 | ||||||
| chr10:102580152
|
A | G | 1 | a0001c0001t0034g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.455-12430A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580152 | ||||||
| chr10:102580298
|
G | A | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-12284G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580298 | ||||||
| chr10:102580315
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.455-12267G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580315 | ||||||
| chr10:102580323
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.455-12259C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580323 | ||||||
| chr10:102580505
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-12077A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580505 | ||||||
| chr10:102580704
|
G | T | 1 | a0001c0002t0002g0006 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.455-11878G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580704 | ||||||
| chr10:102580863
|
A | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.455-11719A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580863 | ||||||
| chr10:102580947
|
C | T | 109 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(106): Show | 109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.455-11635C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102580947 | ||||||
| chr10:102581087
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.455-11495C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102581087 | ||||||
| chr10:102581180
|
CA | C | 39 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0184others(36): Show | 39 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-11371delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581180 | |||||
| chr10:102581180
|
CAA | C | 56 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0232others(53): Show | 56 | HG00280.hp2 HG00558.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.455-11372_455-1137 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581180 | |||||
| chr10:102581180
|
CAAAAAAA others(2): Show |
C | 147 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(144): Show | 147 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.455-11379_455-1137 others(13): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581180 | |||||
| chr10:102581180
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0003g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.455-11381_455-1137 others(15): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581180 | |||||
| chr10:102581180
|
CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-11391_455-1137 others(25): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581180 | |||||
| chr10:102581209
|
A | G | 165 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(162): Show | 165 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.455-11373A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102581209 | ||||||
| chr10:102581219
|
AAG | A | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-11361_455-1136 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102581219 | |||||
| chr10:102581558
|
C | T | 1 | a0001c0001t0012g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.455-11024C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102581558 | ||||||
| chr10:102581559
|
C | T | 2 | a0001c0002t0026g0036a0001c0002t0029g0037 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.455-11023C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102581559 | ||||||
| chr10:102581678
|
T | C | 131 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(128): Show | 131 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.455-10904T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102581678 | ||||||
| chr10:102582088
|
G | C | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-10494G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582088 | ||||||
| chr10:102582130
|
C | T | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-10452C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582130 | ||||||
| chr10:102582218
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-10364T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582218 | ||||||
| chr10:102582449
|
C | T | 77 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(74): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.455-10133C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582449 | ||||||
| chr10:102582527
|
G | A | 5 | a0001c0002t0007g0103a0001c0002t0007g0104a0001c0002t0007g0105others(2): Show | 5 | HG02451.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-10055G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582527 | ||||||
| chr10:102582636
|
C | G | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.455-9946C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582636 | ||||||
| chr10:102582657
|
A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0169 | 2 | NA19011.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.455-9925A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582657 | ||||||
| chr10:102582744
|
A | G | 75 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-9838A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582744 | ||||||
| chr10:102582826
|
T | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.455-9756T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582826 | ||||||
| chr10:102582831
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.455-9751A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102582831 | ||||||
| chr10:102583047
|
G | A | 56 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(53): Show | 56 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.455-9535G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102583047 | ||||||
| chr10:102583671
|
C | A | 56 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(53): Show | 56 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.455-8911C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102583671 | ||||||
| chr10:102583976
|
A | G | 1 | a0001c0001t0005g0080 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.455-8606A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102583976 | ||||||
| chr10:102584523
|
A | T | 1 | a0001c0001t0019g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.455-8059A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102584523 | ||||||
| chr10:102584693
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.455-7889G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102584693 | ||||||
| chr10:102584765
|
G | C | 1 | a0001c0001t0012g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.455-7817G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102584765 | ||||||
| chr10:102584830
|
T | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-7752T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102584830 | ||||||
| chr10:102585071
|
C | T | 2 | a0001c0001t0006g0255a0001c0001t0006g0256 | 2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.455-7511C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585071 | ||||||
| chr10:102585158
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.455-7424C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585158 | ||||||
| chr10:102585200
|
A | G | 1 | a0001c0002t0002g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.455-7382A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585200 | ||||||
| chr10:102585220
|
T | G | 1 | a0001c0001t0034g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.455-7362T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585220 | ||||||
| chr10:102585440
|
C | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.455-7142C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585440 | ||||||
| chr10:102585468
|
G | A | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.455-7114G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585468 | ||||||
| chr10:102585596
|
T | A | 1 | a0001c0002t0028g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.455-6986T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585596 | ||||||
| chr10:102585692
|
G | C | 1 | a0001c0001t0016g0191 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.455-6890G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585692 | ||||||
| chr10:102585888
|
C | CTT | 138 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(135): Show | 138 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.455-6679_455-6678d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102585888 | |||||
| chr10:102585888
|
C | CTTT | 7 | a0001c0001t0001g0164a0001c0002t0002g0063a0001c0002t0002g0098others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-6680_455-6678d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102585888 | |||||
| chr10:102585888
|
C | CTTTT | 5 | a0001c0002t0007g0103a0001c0002t0007g0104a0001c0002t0007g0105others(2): Show | 5 | HG02451.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-6681_455-6678d others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102585888 | |||||
| chr10:102585888
|
CT | C | 50 | a0001c0001t0001g0178a0001c0001t0001g0201a0001c0001t0001g0232others(47): Show | 50 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.455-6678delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102585888 | |||||
| chr10:102585949
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-6633A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102585949 | ||||||
| chr10:102586073
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-6509C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586073 | ||||||
| chr10:102586180
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG03017.hp1 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.455-6402C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586180 | ||||||
| chr10:102586409
|
T | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.455-6173T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586409 | ||||||
| chr10:102586440
|
G | A | 1 | a0001c0002t0002g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.455-6142G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586440 | ||||||
| chr10:102586469
|
C | A | 1 | a0001c0001t0031g0258 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.455-6113C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586469 | ||||||
| chr10:102586603
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.455-5979G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586603 | ||||||
| chr10:102586621
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.455-5961C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586621 | ||||||
| chr10:102586634
|
C | T | 1 | a0001c0002t0002g0001 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.455-5948C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586634 | ||||||
| chr10:102586635
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0206 | 2 | NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.455-5947C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586635 | ||||||
| chr10:102586934
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.455-5648T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102586934 | ||||||
| chr10:102587134
|
G | A | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.455-5448G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587134 | ||||||
| chr10:102587242
|
T | C | 1 | a0001c0002t0002g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.455-5340T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587242 | ||||||
| chr10:102587490
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-5092A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587490 | ||||||
| chr10:102587560
|
C | T | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG02071.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.455-5022C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587560 | ||||||
| chr10:102587584
|
C | T | 4 | a0001c0002t0002g0023a0001c0002t0002g0035a0001c0002t0002g0039others(1): Show | 4 | HG02735.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4998C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587584 | ||||||
| chr10:102587652
|
C | T | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.455-4930C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587652 | ||||||
| chr10:102587711
|
C | G | 1 | a0001c0002t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.455-4871C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102587711 | ||||||
| chr10:102588285
|
C | T | 1 | a0001c0002t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.455-4297C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588285 | ||||||
| chr10:102588392
|
C | A | 1 | a0001c0002t0002g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.455-4190C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588392 | ||||||
| chr10:102588392
|
C | CA | 75 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(72): Show | 75 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.455-4174dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102588392 | |||||
| chr10:102588484
|
G | A | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.455-4098G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588484 | ||||||
| chr10:102588619
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-3963C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588619 | ||||||
| chr10:102588933
|
A | T | 1 | a0001c0001t0006g0251 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.455-3649A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588933 | ||||||
| chr10:102588937
|
T | A | 33 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(30): Show | 33 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.455-3645T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102588937 | ||||||
| chr10:102589091
|
T | TTG | 62 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0242others(59): Show | 62 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.455-3477_455-3476d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589091 | |||||
| chr10:102589236
|
G | A | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.455-3346G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589236 | ||||||
| chr10:102589345
|
C | T | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.455-3237C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589345 | ||||||
| chr10:102589370
|
C | T | 75 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-3212C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589370 | ||||||
| chr10:102589396
|
G | A | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.455-3186G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589396 | ||||||
| chr10:102589442
|
C | CTTT | 8 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0124others(5): Show | 8 | HG01069.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-3121_455-3119d others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTT | 63 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(60): Show | 63 | HG00280.hp1 HG00733.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.455-3122_455-3119d others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTT | 26 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0172others(23): Show | 26 | HG01069.hp2 HG01891.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-3123_455-3119d others(7): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTT | 55 | a0001c0001t0001g0071a0001c0001t0001g0178a0001c0001t0001g0195others(52): Show | 55 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.455-3124_455-3119d others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTTT | 47 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(44): Show | 47 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.455-3125_455-3119d others(9): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTTT others(1): Show |
36 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0198others(33): Show | 36 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.455-3126_455-3119d others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTTT others(2): Show |
25 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0243others(22): Show | 25 | HG00280.hp2 HG00597.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.455-3127_455-3119d others(11): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0250a0001c0001t0006g0224a0001c0001t0008g0022others(1): Show | 4 | HG03225.hp1 NA18522.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-3128_455-3119d others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589442
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.455-3130_455-3119d others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102589442 | |||||
| chr10:102589726
|
G | A | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-2856G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589726 | ||||||
| chr10:102589728
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.455-2854G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589728 | ||||||
| chr10:102589774
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-2808A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589774 | ||||||
| chr10:102589966
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.455-2616T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102589966 | ||||||
| chr10:102590122
|
A | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.455-2460A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590122 | ||||||
| chr10:102590146
|
TTTTTTTC others(7): Show |
T | 3 | a0001c0001t0005g0080a0001c0001t0005g0082a0001c0001t0005g0091 | 3 | HG01074.hp1 HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.455-2429_455-2416d others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102590146 | |||||
| chr10:102590147
|
T | C | 1 | a0001c0001t0013g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-2435T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590147 | ||||||
| chr10:102590158
|
TTC | T | 52 | a0001c0001t0001g0168a0001c0001t0001g0176a0001c0001t0001g0177others(49): Show | 52 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.455-2422_455-2421d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102590158 | |||||
| chr10:102590159
|
TC | T | 185 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0112others(182): Show | 185 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.455-2422delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590159 | ||||||
| chr10:102590160
|
C | T | 21 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0135others(18): Show | 21 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.455-2422C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590160 | ||||||
| chr10:102590191
|
A | C | 1 | a0001c0001t0006g0257 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.455-2391A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590191 | ||||||
| chr10:102590205
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.455-2377A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590205 | ||||||
| chr10:102590312
|
C | G | 1 | a0001c0001t0003g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.455-2270C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590312 | ||||||
| chr10:102590416
|
C | T | 1 | a0001c0002t0002g0061 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.455-2166C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590416 | ||||||
| chr10:102590468
|
A | G | 33 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(30): Show | 33 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.455-2114A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590468 | ||||||
| chr10:102590691
|
T | C | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.455-1891T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590691 | ||||||
| chr10:102590944
|
T | C | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-1638T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590944 | ||||||
| chr10:102590971
|
T | G | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-1611T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590971 | ||||||
| chr10:102590999
|
A | G | 1 | a0001c0001t0003g0250 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.455-1583A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590999 | ||||||
| chr10:102591280
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0212 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455-1302C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591280 | ||||||
| chr10:102591481
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.455-1101A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591481 | ||||||
| chr10:102591498
|
C | CA | 10 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-1068dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102591498 | |||||
| chr10:102591498
|
CA | C | 154 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(151): Show | 154 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.455-1068delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 102591498 | |||||
| chr10:102591610
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.455-972C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591610 | ||||||
| chr10:102591730
|
G | A | 1 | a0001c0001t0024g0252 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.455-852G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591730 | ||||||
| chr10:102591800
|
C | T | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.455-782C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591800 | ||||||
| chr10:102591860
|
G | A | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.455-722G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591860 | ||||||
| chr10:102591959
|
C | G | 1 | a0001c0001t0005g0080 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.455-623C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102591959 | ||||||
| chr10:102592225
|
G | C | 1 | a0001c0002t0002g0025 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.455-357G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102592225 | ||||||
| chr10:102592367
|
C | CCATTT | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.455-215_455-214ins others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102592367 | ||||||
| chr10:102592391
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.455-191G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102592391 | ||||||
| chr10:102592439
|
C | T | 2 | a0001c0001t0010g0052a0001c0001t0010g0137 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.455-143C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102592439 | ||||||
| chr10:102592930
|
A | C | 1 | a0001c0002t0002g0100 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.597+206A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102592930 | ||||||
| chr10:102593058
|
C | T | 2 | a0001c0002t0007g0103a0001c0002t0007g0105 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.597+334C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593058 | ||||||
| chr10:102593168
|
C | T | 2 | a0001c0001t0003g0265a0001c0001t0003g0266 | 2 | HG01070.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.597+444C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593168 | ||||||
| chr10:102593351
|
A | G | 1 | a0001c0001t0009g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.598-285A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593351 | ||||||
| chr10:102593418
|
GGTCAGGC others(12): Show |
G | 1 | a0001c0001t0006g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-217_598-199del others(19): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593418 | ||||||
| chr10:102593439
|
T | A | 1 | a0001c0001t0006g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-197T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593439 | ||||||
| chr10:102593440
|
G | A | 1 | a0001c0001t0006g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-196G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593440 | ||||||
| chr10:102593504
|
G | A | 1 | a0001c0001t0020g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-132G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593504 | ||||||
| chr10:102593568
|
G | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598-68G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 4/11 | chr10 | 102593568 | ||||||
| chr10:102594310
|
T | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.756+245T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594310 | ||||||
| chr10:102594344
|
A | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.756+279A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594344 | ||||||
| chr10:102594553
|
A | G | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756+488A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594553 | ||||||
| chr10:102594667
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.756+602T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594667 | ||||||
| chr10:102594752
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0203others(1): Show | 4 | HG01261.hp1 HG01346.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+687C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594752 | ||||||
| chr10:102594905
|
A | G | 2 | a0001c0002t0002g0087a0001c0002t0028g0086 | 2 | HG01993.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.756+840A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594905 | ||||||
| chr10:102595047
|
T | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.756+982T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595047 | ||||||
| chr10:102595283
|
C | T | 8 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(5): Show | 8 | NA18941.hp1 NA18943.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.756+1218C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595283 | ||||||
| chr10:102595338
|
A | C | 1 | a0001c0001t0005g0078 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.756+1273A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595338 | ||||||
| chr10:102595518
|
A | G | 111 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.756+1453A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595518 | ||||||
| chr10:102595597
|
T | TCTC | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.756+1534_756+1535i others(5): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 102595597 | |||||
| chr10:102595686
|
C | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.757-1454C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595686 | ||||||
| chr10:102595834
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.757-1306G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595834 | ||||||
| chr10:102596428
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0161 | 2 | HG00280.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.757-712C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102596428 | ||||||
| chr10:102596602
|
T | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.757-538T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102596602 | ||||||
| chr10:102597030
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0206 | 2 | NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.757-110C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102597030 | ||||||
| chr10:102597065
|
A | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.757-75A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102597065 | ||||||
| chr10:102597649
|
G | A | 1 | a0001c0001t0005g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.910+356G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102597649 | ||||||
| chr10:102597826
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.910+533C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102597826 | ||||||
| chr10:102597937
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.910+644C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102597937 | ||||||
| chr10:102598013
|
A | G | 2 | a0001c0002t0002g0011a0001c0002t0002g0028 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.910+720A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598013 | ||||||
| chr10:102598045
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.910+752G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598045 | ||||||
| chr10:102598108
|
G | A | 3 | a0001c0001t0004g0108a0001c0001t0004g0126a0001c0001t0004g0127 | 3 | HG02155.hp2 NA18975.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.910+815G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598108 | ||||||
| chr10:102598421
|
G | T | 31 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(28): Show | 31 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.911-1012G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598421 | ||||||
| chr10:102598646
|
T | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.911-787T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598646 | ||||||
| chr10:102598650
|
C | G | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.911-783C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598650 | ||||||
| chr10:102598717
|
G | A | 111 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.911-716G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102598717 | ||||||
| chr10:102599006
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.911-427A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102599006 | ||||||
| chr10:102599096
|
C | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.911-337C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102599096 | ||||||
| chr10:102599240
|
G | C | 1 | a0001c0002t0002g0002 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.911-193G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102599240 | ||||||
| chr10:102599397
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.911-36A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 7/11 | chr10 | 102599397 | ||||||
| chr10:102599582
|
C | T | 1 | a0001c0002t0002g0100 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1022+38C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102599582 | ||||||
| chr10:102599593
|
T | C | 77 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(74): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1022+49T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102599593 | ||||||
| chr10:102599756
|
T | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0148others(3): Show | 6 | NA18955.hp1 NA18959.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022+212T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102599756 | ||||||
| chr10:102600095
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1022+551G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600095 | ||||||
| chr10:102600127
|
C | T | 48 | a0001c0001t0001g0232a0001c0001t0003g0031a0001c0001t0003g0032others(45): Show | 48 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1022+583C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600127 | ||||||
| chr10:102600353
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02027.hp1 NA18941.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1022+809C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600353 | ||||||
| chr10:102600481
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1022+937T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600481 | ||||||
| chr10:102600626
|
G | A | 4 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082others(1): Show | 4 | HG01074.hp1 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022+1082G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600626 | ||||||
| chr10:102600667
|
A | G | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.1022+1123A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600667 | ||||||
| chr10:102600761
|
C | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1022+1217C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600761 | ||||||
| chr10:102600814
|
G | T | 1 | a0001c0002t0002g0026 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1022+1270G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600814 | ||||||
| chr10:102600838
|
C | T | 2 | a0001c0001t0003g0239a0001c0001t0023g0180 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1022+1294C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600838 | ||||||
| chr10:102600916
|
C | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1022+1372C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102600916 | ||||||
| chr10:102601098
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1022+1554T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601098 | ||||||
| chr10:102601159
|
G | C | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1022+1615G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601159 | ||||||
| chr10:102601483
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1022+1939C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601483 | ||||||
| chr10:102601512
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1022+1968G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601512 | ||||||
| chr10:102601694
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1022+2150C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601694 | ||||||
| chr10:102601884
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1022+2340G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601884 | ||||||
| chr10:102601954
|
C | T | 67 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1022+2410C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601954 | ||||||
| chr10:102601980
|
A | G | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1022+2436A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102601980 | ||||||
| chr10:102602678
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1022+3134C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102602678 | ||||||
| chr10:102603062
|
C | G | 1 | a0001c0001t0006g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1022+3518C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603062 | ||||||
| chr10:102603307
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1022+3763A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603307 | ||||||
| chr10:102603362
|
C | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1022+3818C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603362 | ||||||
| chr10:102603536
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1022+3992T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603536 | ||||||
| chr10:102603635
|
T | G | 4 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(1): Show | 4 | HG01070.hp2 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022+4091T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603635 | ||||||
| chr10:102603651
|
A | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1022+4107A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603651 | ||||||
| chr10:102603731
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1022+4187C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603731 | ||||||
| chr10:102603811
|
C | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.1022+4267C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603811 | ||||||
| chr10:102603948
|
T | C | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.1022+4404T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603948 | ||||||
| chr10:102604049
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1022+4505C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604049 | ||||||
| chr10:102604072
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0198 | 2 | HG02155.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1022+4528C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604072 | ||||||
| chr10:102604126
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1022+4582C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604126 | ||||||
| chr10:102604308
|
A | C | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1022+4764A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604308 | ||||||
| chr10:102604466
|
A | G | 15 | a0001c0001t0006g0216a0001c0001t0006g0224a0001c0001t0006g0225others(12): Show | 15 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1022+4922A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604466 | ||||||
| chr10:102604732
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0212a0001c0001t0005g0077 | 3 | HG02280.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1022+5188C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604732 | ||||||
| chr10:102604895
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1022+5351G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102604895 | ||||||
| chr10:102604920
|
CT | C | 128 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(125): Show | 128 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.1022+5400delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102604920 | |||||
| chr10:102604920
|
CTT | C | 128 | a0001c0001t0001g0071a0001c0001t0001g0162a0001c0001t0001g0169others(125): Show | 128 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1022+5399_1022+540 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102604920 | |||||
| chr10:102605139
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1022+5595G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102605139 | ||||||
| chr10:102605525
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1022+5981C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102605525 | ||||||
| chr10:102605550
|
C | T | 2 | a0001c0001t0006g0255a0001c0001t0006g0256 | 2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1022+6006C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102605550 | ||||||
| chr10:102605732
|
TG | T | 110 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(107): Show | 110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1022+6190delG | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102605732 | |||||
| chr10:102605967
|
G | A | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1022+6423G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102605967 | ||||||
| chr10:102606086
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1022+6542G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102606086 | ||||||
| chr10:102606134
|
A | T | 1 | a0001c0001t0031g0258 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1022+6590A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102606134 | ||||||
| chr10:102606285
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1022+6741T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102606285 | ||||||
| chr10:102606596
|
T | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1022+7052T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102606596 | ||||||
| chr10:102607060
|
A | AT | 145 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(142): Show | 145 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.1022+7532dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102607060 | |||||
| chr10:102607210
|
G | C | 1 | a0001c0001t0008g0022 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1022+7666G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607210 | ||||||
| chr10:102607300
|
C | T | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1022+7756C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607300 | ||||||
| chr10:102607324
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1022+7780C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607324 | ||||||
| chr10:102607335
|
C | T | 69 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(66): Show | 69 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.1022+7791C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607335 | ||||||
| chr10:102607620
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1023-7648A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607620 | ||||||
| chr10:102607825
|
C | T | 5 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0221others(2): Show | 5 | HG00280.hp2 HG01169.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1023-7443C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607825 | ||||||
| chr10:102607836
|
A | G | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1023-7432A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607836 | ||||||
| chr10:102607921
|
A | G | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1023-7347A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102607921 | ||||||
| chr10:102608095
|
G | A | 9 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0185others(6): Show | 9 | HG00558.hp1 HG02135.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1023-7173G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608095 | ||||||
| chr10:102608219
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1023-7049G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608219 | ||||||
| chr10:102608230
|
CA | C | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1023-7028delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102608230 | |||||
| chr10:102608255
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1023-7013G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608255 | ||||||
| chr10:102608537
|
A | G | 110 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(107): Show | 110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1023-6731A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608537 | ||||||
| chr10:102608579
|
G | T | 75 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(72): Show | 75 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.1023-6689G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608579 | ||||||
| chr10:102608676
|
G | A | 1 | a0001c0001t0005g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1023-6592G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608676 | ||||||
| chr10:102608999
|
A | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023-6269A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102608999 | ||||||
| chr10:102609152
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.1023-6116T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102609152 | ||||||
| chr10:102609282
|
T | TA | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1023-5983dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102609282 | |||||
| chr10:102609566
|
C | T | 33 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(30): Show | 33 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1023-5702C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102609566 | ||||||
| chr10:102610266
|
A | G | 152 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(149): Show | 152 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.1023-5002A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610266 | ||||||
| chr10:102610364
|
G | T | 1 | a0001c0002t0002g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1023-4904G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610364 | ||||||
| chr10:102610371
|
C | A | 13 | a0001c0001t0001g0213a0001c0001t0005g0020a0001c0001t0005g0021others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023-4897C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610371 | ||||||
| chr10:102610375
|
G | A | 1 | a0001c0003t0003g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1023-4893G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610375 | ||||||
| chr10:102610392
|
C | CAAAAAAA | 258 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(255): Show | 258 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(255): Show |
intron_variant | MODIFIER | c.1023-4871_1023-486 others(11): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102610392 | |||||
| chr10:102610747
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1023-4521A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610747 | ||||||
| chr10:102610831
|
T | G | 1 | a0001c0001t0016g0191 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1023-4437T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610831 | ||||||
| chr10:102610905
|
T | C | 113 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(110): Show | 113 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1023-4363T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610905 | ||||||
| chr10:102611070
|
C | T | 33 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(30): Show | 33 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1023-4198C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102611070 | ||||||
| chr10:102611934
|
C | T | 2 | a0001c0001t0013g0248a0001c0001t0013g0249 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1023-3334C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102611934 | ||||||
| chr10:102612169
|
T | TTG | 47 | a0001c0001t0001g0176a0001c0001t0001g0184a0001c0001t0001g0185others(44): Show | 47 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1023-3060_1023-305 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
T | TTGTG | 12 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0242others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1023-3062_1023-305 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
T | TTGTGTG | 9 | a0001c0001t0001g0179a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG00280.hp2 HG01169.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1023-3064_1023-305 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
TTG | T | 23 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0186others(20): Show | 23 | HG00639.hp1 HG01081.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1023-3060_1023-305 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
TTGTG | T | 11 | a0001c0001t0001g0196a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG00735.hp2 HG01074.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1023-3062_1023-305 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
TTGTGTGT others(1): Show |
T | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1023-3066_1023-305 others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
TTGTGTGT others(9): Show |
T | 77 | a0001c0001t0001g0071a0001c0002t0002g0001a0001c0002t0002g0002others(74): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1023-3074_1023-305 others(20): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612169
|
TTGTGTGT others(11): Show |
T | 74 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(71): Show | 74 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1023-3076_1023-305 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612169 | |||||
| chr10:102612217
|
A | ATG | 150 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(147): Show | 150 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.1023-3037_1023-303 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102612217 | |||||
| chr10:102612266
|
G | A | 1 | a0001c0003t0003g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1023-3002G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102612266 | ||||||
| chr10:102612487
|
A | G | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023-2781A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102612487 | ||||||
| chr10:102612684
|
C | T | 150 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(147): Show | 150 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.1023-2584C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102612684 | ||||||
| chr10:102613108
|
G | A | 13 | a0001c0001t0001g0213a0001c0001t0005g0020a0001c0001t0005g0021others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023-2160G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102613108 | ||||||
| chr10:102613113
|
C | T | 1 | a0001c0001t0005g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023-2155C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102613113 | ||||||
| chr10:102613543
|
A | G | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023-1725A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102613543 | ||||||
| chr10:102613886
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1023-1382G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102613886 | ||||||
| chr10:102614001
|
G | C | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023-1267G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614001 | ||||||
| chr10:102614147
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023-1121G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614147 | ||||||
| chr10:102614238
|
A | G | 2 | a0001c0002t0026g0036a0001c0002t0029g0037 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1023-1030A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614238 | ||||||
| chr10:102614365
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0207 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1023-903T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614365 | ||||||
| chr10:102614489
|
C | T | 6 | a0001c0001t0001g0177a0001c0001t0001g0212a0001c0001t0001g0215others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023-779C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614489 | ||||||
| chr10:102614544
|
C | T | 2 | a0001c0001t0013g0248a0001c0001t0013g0249 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1023-724C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614544 | ||||||
| chr10:102614641
|
C | T | 2 | a0001c0002t0002g0049a0001c0002t0002g0062 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1023-627C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614641 | ||||||
| chr10:102614792
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1023-476C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614792 | ||||||
| chr10:102614861
|
A | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.1023-407A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614861 | ||||||
| chr10:102614879
|
T | TA | 6 | a0001c0001t0001g0138a0001c0001t0001g0172a0001c0001t0001g0198others(3): Show | 6 | HG02027.hp2 HG02717.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023-373dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102614879 | |||||
| chr10:102614879
|
TA | T | 19 | a0001c0001t0001g0243a0001c0001t0003g0250a0001c0001t0006g0216others(16): Show | 19 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1023-373delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 102614879 | |||||
| chr10:102614880
|
A | T | 1 | a0001c0002t0002g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1023-388A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614880 | ||||||
| chr10:102614895
|
AT | A | 9 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0147others(6): Show | 9 | HG01069.hp2 HG01943.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1023-372delT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614895 | ||||||
| chr10:102614896
|
T | A | 142 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(139): Show | 142 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.1023-372T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614896 | ||||||
| chr10:102614939
|
C | T | 13 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095others(10): Show | 13 | HG01928.hp1 HG01952.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023-329C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614939 | ||||||
| chr10:102614941
|
C | T | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1023-327C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102614941 | ||||||
| chr10:102615058
|
G | C | 67 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(64): Show | 67 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.1023-210G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102615058 | ||||||
| chr10:102615245
|
C | G | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1023-23C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102615245 | ||||||
| chr10:102615501
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1157+99G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102615501 | ||||||
| chr10:102615515
|
C | T | 1 | a0001c0002t0002g0040 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1157+113C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102615515 | ||||||
| chr10:102615648
|
T | G | 5 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0221others(2): Show | 5 | HG00280.hp2 HG01169.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+246T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102615648 | ||||||
| chr10:102615820
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1157+418A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102615820 | ||||||
| chr10:102615977
|
TGC | T | 111 | a0001c0001t0001g0116a0001c0001t0001g0176a0001c0001t0001g0177others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1157+576_1157+577d others(4): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102615977 | ||||||
| chr10:102616270
|
C | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1157+868C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102616270 | ||||||
| chr10:102616304
|
A | G | 1 | a0001c0002t0002g0088 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1157+902A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102616304 | ||||||
| chr10:102617169
|
A | AGGGCATG others(127): Show |
1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1158-98_1158-97ins others(134): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr10 | 102617169 | |||||
| chr10:102617189
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0177a0001c0001t0001g0212others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158-101C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 9/11 | chr10 | 102617189 | ||||||
| chr10:102617638
|
C | T | 1 | a0001c0001t0003g0221 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1296+210C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102617638 | ||||||
| chr10:102618002
|
T | C | 112 | a0001c0001t0001g0116a0001c0001t0001g0176a0001c0001t0001g0177others(109): Show | 112 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1296+574T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618002 | ||||||
| chr10:102618005
|
T | C | 264 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.1296+577T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618005 | ||||||
| chr10:102618086
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1296+658G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618086 | ||||||
| chr10:102618151
|
A | T | 1 | a0001c0001t0003g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1296+723A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618151 | ||||||
| chr10:102618377
|
A | G | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1296+949A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618377 | ||||||
| chr10:102618524
|
C | T | 1 | a0001c0001t0005g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1296+1096C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618524 | ||||||
| chr10:102618606
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01255.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1296+1178G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618606 | ||||||
| chr10:102618781
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1296+1353C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618781 | ||||||
| chr10:102618783
|
C | T | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1296+1355C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618783 | ||||||
| chr10:102618806
|
G | T | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1296+1378G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618806 | ||||||
| chr10:102618851
|
G | A | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1296+1423G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618851 | ||||||
| chr10:102618931
|
C | CGT | 38 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0134others(35): Show | 38 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+1550_1296+155 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGT | 38 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(35): Show | 38 | HG01175.hp2 HG01943.hp1 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.1296+1548_1296+155 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGT | 28 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0167others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1296+1546_1296+155 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(1): Show |
28 | a0001c0001t0001g0133a0001c0001t0001g0168a0001c0001t0001g0243others(25): Show | 28 | HG00544.hp1 HG01433.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.1296+1544_1296+155 others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(3): Show |
13 | a0001c0001t0001g0186a0001c0001t0001g0210a0001c0001t0005g0082others(10): Show | 13 | HG01074.hp2 HG02056.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1296+1542_1296+155 others(14): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(5): Show |
8 | a0001c0001t0001g0254a0001c0001t0016g0191a0001c0002t0002g0001others(5): Show | 8 | HG00597.hp2 HG02071.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+1540_1296+155 others(16): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(7): Show |
4 | a0001c0001t0004g0107a0001c0002t0002g0049a0001c0002t0002g0059others(1): Show | 4 | HG02074.hp2 HG02273.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+1538_1296+155 others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(9): Show |
1 | a0001c0002t0002g0026 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1296+1536_1296+155 others(20): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(11): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0116a0001c0001t0001g0253 | 3 | HG01358.hp2 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1296+1534_1296+155 others(22): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(13): Show |
1 | a0001c0002t0002g0070 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1296+1532_1296+155 others(24): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
C | CGTGTGTG others(23): Show |
1 | a0001c0002t0002g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1296+1522_1296+155 others(34): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
CGT | C | 27 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0151others(24): Show | 27 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1296+1550_1296+155 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
CGTGT | C | 26 | a0001c0001t0001g0232a0001c0001t0003g0181a0001c0001t0003g0218others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1296+1548_1296+155 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
CGTGTGT | C | 10 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0217others(7): Show | 10 | HG00280.hp2 HG00544.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+1546_1296+155 others(10): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1296+1544_1296+155 others(12): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618931
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1296+1538_1296+155 others(18): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102618931 | |||||
| chr10:102618933
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1296+1505T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618933 | ||||||
| chr10:102618935
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1296+1507T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618935 | ||||||
| chr10:102618993
|
G | A | 151 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(148): Show | 151 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.1296+1565G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618993 | ||||||
| chr10:102619221
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1296+1793C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102619221 | ||||||
| chr10:102619252
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1296+1824C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102619252 | ||||||
| chr10:102619269
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1296+1841G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102619269 | ||||||
| chr10:102619762
|
G | A | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1296+2334G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102619762 | ||||||
| chr10:102619831
|
G | A | 2 | a0001c0001t0012g0236a0001c0001t0012g0262 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1296+2403G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102619831 | ||||||
| chr10:102620271
|
G | A | 1 | a0001c0002t0035g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1296+2843G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102620271 | ||||||
| chr10:102620929
|
G | A | 150 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(147): Show | 150 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.1296+3501G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102620929 | ||||||
| chr10:102621396
|
G | C | 1 | a0001c0001t0005g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1296+3968G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102621396 | ||||||
| chr10:102621475
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1296+4047A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102621475 | ||||||
| chr10:102621639
|
C | CCACTGCC others(59): Show |
1 | a0001c0002t0002g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1296+4212_1296+427 others(70): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102621639 | |||||
| chr10:102621749
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1296+4321T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102621749 | ||||||
| chr10:102621822
|
G | A | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1296+4394G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102621822 | ||||||
| chr10:102622185
|
A | T | 1 | a0001c0001t0006g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1296+4757A>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622185 | ||||||
| chr10:102622251
|
C | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1296+4823C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622251 | ||||||
| chr10:102622407
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1297-4768C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622407 | ||||||
| chr10:102622615
|
G | A | 3 | a0001c0001t0014g0017a0001c0001t0014g0018a0001c0001t0033g0069 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1297-4560G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622615 | ||||||
| chr10:102622710
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1297-4465T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622710 | ||||||
| chr10:102622718
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1297-4457C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622718 | ||||||
| chr10:102622823
|
GA | G | 73 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(70): Show | 73 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1297-4334delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622823 | |||||
| chr10:102622823
|
GAA | G | 78 | a0001c0001t0001g0071a0001c0001t0001g0132a0001c0001t0001g0148others(75): Show | 78 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.1297-4335_1297-433 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622823 | |||||
| chr10:102622828
|
A | G | 2 | a0001c0002t0002g0026a0001c0002t0002g0043 | 2 | HG02809.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1297-4347A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622828 | ||||||
| chr10:102622888
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1297-4287G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622888 | ||||||
| chr10:102622916
|
A | G | 121 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(118): Show | 121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1297-4259A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622916 | ||||||
| chr10:102622931
|
C | T | 1 | a0001c0001t0023g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1297-4244C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622931 | ||||||
| chr10:102622956
|
A | C | 1 | a0001c0001t0004g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1297-4219A>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102622956 | ||||||
| chr10:102622991
|
C | CA | 6 | a0001c0001t0001g0167a0001c0001t0003g0228a0001c0001t0003g0240others(3): Show | 6 | HG00544.hp2 HG01433.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-4159dupA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622991 | |||||
| chr10:102622991
|
CA | C | 78 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(75): Show | 78 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1297-4159delA | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622991 | |||||
| chr10:102622991
|
CAA | C | 59 | a0001c0001t0001g0071a0001c0001t0001g0155a0001c0001t0001g0163others(56): Show | 59 | HG00544.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1297-4160_1297-415 others(6): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622991 | |||||
| chr10:102622991
|
CAAAA | C | 11 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(8): Show | 11 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1297-4162_1297-415 others(8): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102622991 | |||||
| chr10:102623080
|
G | A | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1297-4095G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102623080 | ||||||
| chr10:102624272
|
G | A | 78 | a0001c0001t0001g0071a0001c0001t0001g0155a0001c0002t0002g0001others(75): Show | 78 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.1297-2903G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102624272 | ||||||
| chr10:102624413
|
T | A | 1 | a0001c0001t0004g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1297-2762T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102624413 | ||||||
| chr10:102624454
|
C | CT | 68 | a0001c0001t0001g0071a0001c0001t0001g0155a0001c0002t0002g0001others(65): Show | 68 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1297-2720dupT | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 102624454 | |||||
| chr10:102624579
|
AAAAATGG others(59): Show |
A | 1 | a0001c0002t0002g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1297-2595_1297-253 others(70): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102624579 | ||||||
| chr10:102624580
|
A | G | 64 | a0001c0001t0001g0071a0001c0001t0001g0155a0001c0002t0002g0001others(61): Show | 64 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1297-2595A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102624580 | ||||||
| chr10:102624646
|
C | G | 1 | a0001c0002t0002g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1297-2529C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102624646 | ||||||
| chr10:102625203
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0147 | 2 | NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1297-1972C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625203 | ||||||
| chr10:102625283
|
C | T | 1 | a0001c0001t0004g0128 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1297-1892C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625283 | ||||||
| chr10:102625284
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1297-1891G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625284 | ||||||
| chr10:102625375
|
G | A | 53 | a0001c0001t0001g0211a0001c0001t0001g0242a0001c0001t0001g0243others(50): Show | 53 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1297-1800G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625375 | ||||||
| chr10:102625476
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0146others(1): Show | 4 | NA18944.hp2 NA18979.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1699C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625476 | ||||||
| chr10:102625546
|
C | T | 1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1297-1629C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625546 | ||||||
| chr10:102625627
|
A | G | 267 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0111others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(264): Show |
intron_variant | MODIFIER | c.1297-1548A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625627 | ||||||
| chr10:102625641
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0177a0001c0001t0001g0212others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297-1534G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625641 | ||||||
| chr10:102625865
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0177a0001c0001t0001g0212others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297-1310C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102625865 | ||||||
| chr10:102626268
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1297-907G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102626268 | ||||||
| chr10:102626395
|
A | G | 77 | a0001c0001t0004g0114a0001c0002t0002g0001a0001c0002t0002g0002others(74): Show | 77 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1297-780A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102626395 | ||||||
| chr10:102626552
|
T | A | 111 | a0001c0001t0001g0116a0001c0001t0001g0176a0001c0001t0001g0177others(108): Show | 111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1297-623T>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102626552 | ||||||
| chr10:102626795
|
A | G | 5 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(2): Show | 5 | HG01928.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297-380A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102626795 | ||||||
| chr10:102627262
|
T | C | 189 | a0001c0001t0001g0116a0001c0001t0001g0176a0001c0001t0001g0177others(186): Show | 189 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.1365+19T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627262 | ||||||
| chr10:102627346
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1365+103G>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627346 | ||||||
| chr10:102627349
|
C | T | 2 | a0001c0001t0006g0257a0001c0001t0031g0258 | 2 | NA18952.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1365+106C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627349 | ||||||
| chr10:102627555
|
C | T | 1 | a0001c0002t0002g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1365+312C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627555 | ||||||
| chr10:102627823
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18941.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1365+580C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627823 | ||||||
| chr10:102627951
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1365+708C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627951 | ||||||
| chr10:102627978
|
C | T | 76 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(73): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1365+735C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102627978 | ||||||
| chr10:102628199
|
C | A | 10 | a0001c0002t0002g0098a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1365+956C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102628199 | ||||||
| chr10:102628743
|
G | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0092 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1366-1323G>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102628743 | ||||||
| chr10:102628792
|
C | T | 44 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0115others(41): Show | 44 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1366-1274C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102628792 | ||||||
| chr10:102628856
|
T | TAGAAAAG others(311): Show |
1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1366-1199_1366-119 others(322): Show |
SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 102628856 | |||||
| chr10:102628920
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0146others(1): Show | 4 | NA18944.hp2 NA18979.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-1146C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102628920 | ||||||
| chr10:102628953
|
T | C | 76 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(73): Show | 76 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1366-1113T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102628953 | ||||||
| chr10:102629152
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0085 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1366-914G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102629152 | ||||||
| chr10:102629461
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1366-605G>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102629461 | ||||||
| chr10:102629526
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366-540C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102629526 |