Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1452 | 189 | 45 | 47 | 62 | 6 | 27 | SUFU_chr10_102498972_102638535 | SUFU | ATGGC others(1447): Show |
chr10 | 102498972 | 102638535 | ||
| a0001c0002 | 0/0 | 1452 | 76 | 15 | 9 | 42 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | ATGGC others(1447): Show |
chr10 | 102498972 | 102638535 | ||
| a0001c0003 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | ATGGC others(1447): Show |
chr10 | 102498972 | 102638535 | ||
| a0001c0004 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | ATGGC others(1447): Show |
chr10 | 102498972 | 102638535 | ||
| a0001c0005 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | ATGGC others(1447): Show |
chr10 | 102498972 | 102638535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5016 | 93 | 14 | 24 | 32 | 4 | 18 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0003 | 0/0 | 5016 | 24 | 6 | 9 | 4 | 2 | 3 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0004 | 0/0 | 5016 | 20 | 0 | 5 | 15 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0005 | 0/0 | 5016 | 13 | 11 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGATT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0006 | 0/0 | 5016 | 12 | 0 | 0 | 8 | 0 | 4 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0008 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0009 | 0/0 | 5016 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0010 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0011 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0012 | 0/0 | 5016 | 2 | 0 | 2 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0013 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0014 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0015 | 0/1 | 5016 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0016 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0017 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0018 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0019 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0020 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0021 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0022 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0023 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0024 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0031 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0032 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0001t0033 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGATT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0002 | 0/0 | 5016 | 64 | 7 | 8 | 39 | 2 | 8 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0007 | 0/0 | 5016 | 5 | 5 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0025 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0026 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0027 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0028 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0029 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5052): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0030 | 0/0 | 5016 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0002t0034 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGATT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0003t0003 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0004t0003 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| a0001c0005t0004 | 0/0 | 5016 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | AGACT others(5011): Show |
chr10 | 102498972 | 102638535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0205 | 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 |
| a0001c0001t0001g0233 | 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 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0248 | 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 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0004g0113 | 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 |
| a0001c0001t0004g0115 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0006g0226 | 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 |
| a0001c0001t0006g0236 | 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 |
| a0001c0001t0010g0053 | 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 |
| a0001c0001t0012g0237 | 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 |
| a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0013g0250 | 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 |
| a0001c0001t0015g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0018g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0019g0204 | 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 |
| a0001c0001t0022g0234 | 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 |
| a0001c0001t0032g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0001t0033g0076 | 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 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0026g0034 | 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 |
| a0001c0002t0029g0035 | 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 |
| a0001c0002t0034g0084 | 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 |
| a0001c0004t0003g0227 | 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 | g0204 | 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 | g0011 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0193 | 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 | g0233 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0237 | 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 | g0116 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0044 | 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 | g0246 | AMR | PUR | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0078 | 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 | g0238 | 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 | g0111 | 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 | g0194 | 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 | g0133 | 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 | g0234 | AMR | CLM | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0046 | 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 | g0228 | 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 | t0018 | 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 | g0114 | 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 | g0039 | 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 | g0110 | EAS | KHV | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0048 | 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 | g0235 | 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 | g0128 | 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 | g0080 | 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 | g0250 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02615 | hp2 | a0001 | c0002 | t0026 | g0034 | 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 | g0035 | 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 | t0001 | g0242 | 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 | g0053 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0042 | 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 | g0249 | 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 | g0082 | AFR | GWD | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0232 | 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 | t0034 | 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 | g0079 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0037 | 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 | g0109 | AFR | MSL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0231 | 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 | g0112 | AFR | ESN | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0230 | 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 | g0108 | 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 | g0167 | 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 | g0168 | 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 | g0045 | 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 | g0132 | SAS | PJL | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0036 | SAS | BEB | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0248 | 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 | g0227 | SAS | STU | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0040 | 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 | g0081 | 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 | g0226 | 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 | g0224 | 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 | g0203 | 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 | g0049 | 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 | t0017 | 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 | g0205 | 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 | g0225 | 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 | g0236 | 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 | g0041 | 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 | g0012 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0229 | 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 | t0033 | 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 | g0129 | 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 | g0127 | 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 | g0130 | 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 | g0043 | 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 | g0113 | 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 | g0047 | 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 | g0038 | EAS | JPT | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0117 | 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 | g0245 | 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 | t0032 | 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 | a0001 | c0001 | t0015 | g0206 | REF | REF | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0068 | REF | REF | SUFU_chr10_102498972_102638535 | SUFU | chr10 | 102498972 | 102638535 |
| view | 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 |
|---|
| view | 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 |
| view | 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 | a0001c0001t0005 a0001c0001t0033 a0001c0002t0034 |
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 | a0001c0001t0014 a0001c0001t0032 |
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 | ||||||
| chr10:102630273 | C | T | 2 | a0001c0001t0004 a0001c0005t0004 |
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 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0025 others(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 | a0001c0001t0016 | 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 | a0001c0002t0034 | 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 | a0001c0001t0017 | 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 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(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 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0025 others(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 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0025 others(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 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0025 others(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 | a0001c0001t0001 | 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 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0012 others(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 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0022 others(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 | a0001c0001t0010 a0001c0001t0032 a0001c0001t0033 |
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 | a0001c0001t0018 | 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 |
| view | 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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0179 a0001c0001t0003g0181 a0001c0001t0003g0182 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0116 a0001c0001t0004g0117 |
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 | a0001c0001t0004g0115 | 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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | 32 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(29): Show |
32 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(29): 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 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
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 | a0001c0001t0006g0255 a0001c0001t0006g0256 a0001c0001t0006g0257 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0087 a0001c0002t0028g0086 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0207 a0001c0001t0005g0020 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | 265 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(262): Show |
265 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(262): 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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | |||||||
| chr10:102510502 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0034g0084 | 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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0254 a0001c0001t0006g0251 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0113 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0013g0249 a0001c0001t0013g0250 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | |||||||
| chr10:102514186 | A | G | 74 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | |||||||
| chr10:102514973 | C | G | 83 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0013g0249 a0001c0001t0013g0250 |
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 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0001g0071 a0001c0001t0005g0020 a0001c0001t0005g0021 others(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 | 84 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(81): Show |
84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): 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 | a0001c0001t0001g0166 a0001c0002t0002g0098 a0001c0002t0002g0099 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
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 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0260 a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0248 a0001c0001t0003g0183 a0001c0001t0003g0238 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0196 others(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 |
30 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(27): Show |
30 | HG00558.hp1 HG00597.hp1 HG00642.hp1 others(27): 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 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0215 others(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 | GTCTA | 4 | a0001c0001t0008g0022 a0001c0001t0014g0017 a0001c0001t0014g0018 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0111 a0001c0002t0002g0002 |
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 | 75 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0184 others(72): Show |
75 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(72): 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 | a0001c0001t0001g0186 a0001c0001t0017g0191 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): 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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | 89 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(86): Show |
89 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(86): 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 | a0001c0001t0001g0147 a0001c0002t0002g0098 a0001c0002t0002g0099 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | 108 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(105): Show |
108 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(105): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0111 a0001c0001t0004g0093 a0001c0001t0004g0094 others(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 | a0001c0001t0006g0216 a0001c0001t0006g0225 a0001c0001t0006g0226 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0074 others(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 | 69 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0184 others(66): Show |
69 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(66): 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0028 |
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 | a0001c0001t0001g0248 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0131 a0001c0005t0004g0165 |
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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0074 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0006g0216 a0001c0001t0006g0261 |
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 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0246 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0169 |
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 | |||||||
| chr10:102522098 | C | T | 1 | a0001c0001t0022g0234 | 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 | a0001c0001t0012g0237 a0001c0001t0012g0262 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | |||||||
| chr10:102523104 | G | A | 69 | a0001c0001t0001g0071 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0172 |
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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.317+14814C>A | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102524117 | |||||||
| chr10:102524260 | C | G | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(89): 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 | a0001c0001t0012g0262 a0001c0002t0002g0060 a0001c0002t0002g0061 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 181 | a0001c0001t0001g0071 a0001c0001t0001g0176 a0001c0001t0001g0177 others(178): Show |
181 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(178): 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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0001t0006g0236 | 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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | 94 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(91): Show |
94 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(91): 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 | a0001c0002t0002g0058 a0001c0002t0002g0059 |
2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.317+16800C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102526103 | |||||||
| chr10:102526363 | G | A | 9 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0215 a0001c0001t0003g0181 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0009g0189 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0157 a0001c0001t0001g0211 others(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 | 35 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(32): Show |
35 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(32): 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 | a0001c0001t0001g0186 a0001c0001t0001g0199 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0002t0002g0054 a0001c0002t0002g0055 a0001c0002t0002g0061 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | 45 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0176 others(42): Show |
45 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(42): 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 | a0001c0001t0001g0190 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0004g0096 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | |||||||
| chr10:102529019 | G | T | 4 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0111 others(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 | a0001c0001t0005g0078 a0001c0001t0005g0080 a0001c0001t0005g0082 others(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 | a0001c0001t0033g0076 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | 92 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
92 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(89): 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 | a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0013g0249 a0001c0001t0013g0250 |
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 | a0001c0002t0002g0099 a0001c0002t0002g0100 a0001c0002t0002g0101 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 162 | a0001c0001t0001g0071 a0001c0001t0001g0118 a0001c0001t0001g0132 others(159): Show |
162 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(159): 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | |||||||
| chr10:102531703 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0016g0232 | 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 | a0001c0001t0019g0204 | 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 | a0001c0001t0010g0053 | 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 | a0001c0001t0010g0053 a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0009g0189 others(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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0187 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0224 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0006g0225 a0001c0001t0006g0226 a0001c0001t0006g0236 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0006g0216 a0001c0001t0006g0261 |
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 | a0001c0001t0019g0204 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0004g0130 | 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 | 55 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(52): Show |
55 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(52): 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 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0198 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0223 others(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 | a0001c0001t0011g0067 a0001c0002t0002g0098 a0001c0002t0002g0099 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0023 a0001c0002t0002g0037 a0001c0002t0002g0052 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0112 | 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 | 221 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0001g0109 others(218): Show |
221 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(218): 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 | a0001c0001t0033g0076 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 21 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0184 others(18): Show |
21 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.318-13309C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536661 | |||||||
| chr10:102536662 | T | G | 21 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0184 others(18): Show |
21 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.318-13308T>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102536662 | |||||||
| chr10:102536712 | T | A | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): 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 | a0001c0002t0002g0036 | 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 | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): 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 | a0001c0002t0002g0012 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0198 a0001c0001t0005g0020 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | 193 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(190): Show |
193 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.318-11936T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102538034 | |||||||
| chr10:102538198 | C | T | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0003g0231 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 a0001c0002t0002g0039 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0228 | 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 | 193 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(190): Show |
193 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(190): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0173 |
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 | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): Show |
intron_variant | MODIFIER | c.318-8563delC | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 2/11 | chr10 | 102541406 | |||||||
| chr10:102541555 | C | T | 1 | a0001c0001t0006g0235 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0027 a0001c0002t0002g0029 a0001c0002t0002g0049 others(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 | 37 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0185 others(34): Show |
37 | HG00544.hp1 HG00558.hp1 HG00741.hp1 others(34): 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 | a0001c0001t0001g0116 a0001c0001t0001g0167 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0118 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0187 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0071 a0001c0001t0003g0183 a0001c0001t0010g0053 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0027 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0148 a0001c0001t0001g0150 others(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 | 167 | a0001c0001t0001g0071 a0001c0001t0001g0176 a0001c0001t0001g0177 others(164): Show |
167 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(164): 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 | a0001c0002t0002g0040 | 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 | a0001c0001t0019g0204 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 258 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(255): Show |
258 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(255): 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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0039 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0247 | 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 | 53 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(50): Show |
53 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(50): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0034g0084 | 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 | a0001c0001t0004g0128 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | 262 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(259): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | 108 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0176 others(105): Show |
108 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(105): 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 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0001g0205 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0100 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0004t0003g0227 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0002t0002g0012 | 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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0005g0081 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0034g0084 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0248 | 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 | 109 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(106): Show |
109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): 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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0002t0034g0084 | 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 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | 46 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(43): Show |
46 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(43): 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 | a0001c0001t0001g0186 a0001c0001t0005g0073 a0001c0001t0005g0078 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0143 a0001c0001t0001g0169 others(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 | a0001c0002t0002g0007 a0001c0002t0002g0015 a0001c0002t0002g0019 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0156 a0001c0001t0005g0078 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0006g0216 others(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 | a0001c0002t0002g0026 a0001c0002t0002g0042 |
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 | a0001c0002t0002g0044 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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 | a0001c0001t0010g0053 a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0002t0002g0012 a0001c0002t0002g0028 |
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 | a0001c0001t0019g0204 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0233 a0001c0001t0003g0031 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0009g0189 others(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 | a0001c0001t0001g0071 a0001c0001t0010g0053 a0001c0002t0002g0001 others(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 | a0001c0001t0006g0235 | 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 | a0001c0002t0002g0019 a0001c0002t0002g0047 a0001c0002t0002g0051 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0002t0002g0049 | 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 | a0001c0001t0001g0243 | 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 | a0001c0002t0002g0044 | 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 | a0001c0001t0005g0079 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0146 others(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 | 49 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(46): Show |
49 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(46): 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 | 106 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0142 others(103): Show |
106 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0010g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.454+6067C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102556173 | |||||||
| chr10:102556220 | CT | C | 67 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0006g0236 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0114 | 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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0167 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0002g0043 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | 52 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(49): Show |
52 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(49): 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 | 52 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(49): Show |
52 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(49): 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 | a0001c0001t0004g0127 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0147 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0006g0216 a0001c0001t0006g0225 a0001c0001t0006g0226 others(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 | a0001c0001t0005g0020 a0001c0001t0005g0075 |
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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0162 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0004g0110 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | 264 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(261): Show |
264 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(261): 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 | a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0003g0239 | 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 | a0001c0001t0004g0113 | 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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0006g0216 a0001c0001t0006g0225 a0001c0001t0006g0226 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0016g0232 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0002t0002g0011 a0001c0002t0002g0013 a0001c0002t0002g0014 |
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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | a0001c0002t0002g0037 a0001c0002t0002g0052 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0009g0189 a0001c0001t0009g0192 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | CTTTT | 31 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0001g0187 others(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 | ||||||
| chr10:102567088 | T | G | 1 | a0001c0002t0002g0012 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0010g0053 a0001c0001t0010g0137 a0001c0001t0033g0076 |
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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | |||||||
| chr10:102568611 | C | T | 10 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0004t0003g0227 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0233 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0195 others(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 | CAAAAA | 11 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0224 a0001c0001t0003g0229 a0001c0001t0003g0239 others(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 | a0001c0001t0016g0232 a0001c0002t0002g0029 a0001c0002t0002g0036 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0171 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0154 a0001c0001t0021g0153 |
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 | a0001c0001t0001g0112 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0101 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0144 a0001c0001t0004g0113 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0248 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0148 others(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 | a0001c0001t0013g0250 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0242 a0001c0001t0003g0221 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0118 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0214 a0001c0001t0011g0067 a0001c0001t0014g0018 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0196 others(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 | a0001c0001t0004g0127 a0001c0001t0004g0129 a0001c0001t0004g0130 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0199 a0001c0001t0001g0259 others(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 | a0001c0001t0014g0018 a0001c0001t0018g0200 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 107 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0136 others(104): Show |
107 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(104): 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 | a0001c0001t0001g0123 a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0152 others(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 | 111 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): 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 | a0001c0002t0002g0012 a0001c0002t0002g0028 |
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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0002t0002g0027 a0001c0002t0002g0029 a0001c0002t0002g0049 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0265 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0188 a0001c0001t0001g0202 others(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 | a0001c0001t0003g0183 a0001c0001t0003g0217 a0001c0001t0031g0258 others(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 | 71 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(68): Show |
71 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(68): 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 | a0001c0001t0001g0213 a0001c0001t0003g0241 a0001c0001t0006g0216 others(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 | a0001c0001t0012g0237 | 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 | 46 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(43): Show |
46 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(43): 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 | a0001c0001t0005g0078 a0001c0001t0005g0079 a0001c0001t0005g0082 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0007 others(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 | a0001c0002t0002g0054 a0001c0002t0002g0055 a0001c0002t0002g0060 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | 108 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(105): Show |
108 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(105): 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0011 a0001c0002t0002g0013 a0001c0002t0002g0014 |
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 | a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0136 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 259 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(256): Show |
259 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(256): 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 | 107 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(104): Show |
107 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(104): 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 | a0001c0001t0012g0237 a0001c0001t0012g0262 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0233 a0001c0001t0003g0217 a0001c0001t0003g0223 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0133 others(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 | a0001c0001t0032g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.455-21196C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102571386 | |||||||
| chr10:102571576 | G | C | 3 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | |||||||
| chr10:102572001 | 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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0006g0255 a0001c0001t0006g0256 |
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 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0073 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | |||||||
| chr10:102574587 | T | G | 1 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0016g0232 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0123 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0003g0224 | 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 | 124 | a0001c0001t0001g0071 a0001c0001t0001g0176 a0001c0001t0001g0177 others(121): Show |
124 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(121): 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 | a0001c0002t0002g0001 a0001c0002t0002g0041 a0001c0002t0002g0048 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(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 | 254 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(251): Show |
254 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(251): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 109 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(106): Show |
109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | ||||||
| chr10:102577762 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0005g0082 a0001c0001t0005g0091 |
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 | 110 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0003g0218 a0001c0001t0003g0241 a0001c0001t0023g0180 |
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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0009g0189 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0248 a0001c0001t0003g0181 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0233 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0243 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | 110 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0033g0076 | 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | 108 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(105): Show |
108 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(105): 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 | a0001c0001t0001g0107 | 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 | 38 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0184 others(35): Show |
38 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(35): 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0012g0237 | 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 | a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0002t0007g0103 a0001c0002t0007g0104 a0001c0002t0007g0105 others(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 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | a0001c0001t0005g0078 | 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 | a0001c0001t0019g0204 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0012g0237 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0006g0255 a0001c0001t0006g0256 |
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 | a0001c0001t0033g0076 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0017g0191 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0164 a0001c0002t0002g0063 a0001c0002t0002g0098 others(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 | a0001c0002t0007g0103 a0001c0002t0007g0104 a0001c0002t0007g0105 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0201 a0001c0001t0001g0233 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0036 | 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 | a0001c0001t0006g0235 | 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 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 |
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 | a0001c0002t0002g0023 a0001c0002t0002g0037 a0001c0002t0002g0052 others(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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | 32 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(29): Show |
32 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(29): 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 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0242 others(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 | ||||||
| chr10:102589345 | C | T | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0124 others(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 | CTTTTT | 26 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0178 a0001c0001t0001g0195 others(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 | 46 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(43): Show |
46 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(43): 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 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0233 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | a0001c0001t0003g0224 a0001c0001t0006g0225 a0001c0001t0008g0022 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0005g0078 a0001c0001t0005g0080 a0001c0001t0005g0091 |
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 | a0001c0001t0013g0249 | 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 | 51 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0001g0177 others(48): Show |
51 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(48): 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 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 32 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(29): Show |
32 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.455-2114A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 3/11 | chr10 | 102590468 | |||||||
| chr10:102590691 | T | C | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0003g0224 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0212 |
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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0005g0078 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0010g0053 a0001c0001t0010g0137 |
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 | a0001c0002t0007g0103 a0001c0002t0007g0105 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 3 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0207 |
3 | HG01261.hp1 HG01346.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.756+687C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102594752 | |||||||
| chr10:102594905 | A | G | 2 | a0001c0002t0002g0087 a0001c0002t0028g0086 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(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 | a0001c0001t0005g0079 | 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 | 110 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.756+1453A>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 6/11 | chr10 | 102595518 | |||||||
| chr10:102595686 | C | G | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0133 a0001c0001t0001g0161 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0002t0002g0012 a0001c0002t0002g0028 |
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 | a0001c0001t0004g0115 a0001c0001t0004g0126 a0001c0001t0004g0128 |
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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 110 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): 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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0233 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | a0001c0001t0005g0078 a0001c0001t0005g0080 a0001c0001t0005g0082 others(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 | |||||||
| chr10:102600761 | C | T | 151 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0003g0241 a0001c0001t0023g0180 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0004g0110 | 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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.1022+4267C>G | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102603811 | |||||||
| chr10:102603948 | T | C | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0198 |
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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0006g0216 a0001c0001t0006g0225 a0001c0001t0006g0226 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0212 a0001c0001t0005g0077 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | 127 | a0001c0001t0001g0071 a0001c0001t0001g0162 a0001c0001t0001g0169 others(124): Show |
127 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(124): 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0006g0255 a0001c0001t0006g0256 |
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 | 109 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(106): Show |
109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0221 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 109 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(106): Show |
109 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(106): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | |||||||
| chr10:102609282 | T | TA | 152 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 32 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(29): Show |
32 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(29): 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0213 a0001c0001t0005g0020 a0001c0001t0005g0021 others(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 | |||||||
| chr10:102610747 | A | G | 1 | a0001c0001t0001g0112 | 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 | a0001c0001t0017g0191 | 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 | 112 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(109): Show |
112 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1023-4363T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 8/11 | chr10 | 102610905 | |||||||
| chr10:102611070 | C | T | 32 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(29): Show |
32 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(29): 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 | a0001c0001t0013g0249 a0001c0001t0013g0250 |
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 | 46 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0001g0185 others(43): Show |
46 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(43): 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 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0210 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0213 a0001c0001t0005g0020 a0001c0001t0005g0021 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0026g0034 a0001c0002t0029g0035 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0177 a0001c0001t0001g0212 a0001c0001t0001g0215 others(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 | a0001c0001t0013g0249 a0001c0001t0013g0250 |
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 | a0001c0002t0002g0048 a0001c0002t0002g0062 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0138 a0001c0001t0001g0172 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0245 a0001c0001t0003g0224 a0001c0001t0006g0216 others(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 | a0001c0002t0002g0045 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0095 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0002t0002g0038 | 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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0221 others(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 | 110 | a0001c0001t0001g0112 a0001c0001t0001g0176 a0001c0001t0001g0177 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0177 a0001c0001t0001g0212 others(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 | 111 | a0001c0001t0001g0112 a0001c0001t0001g0176 a0001c0001t0001g0177 others(108): Show |
111 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1296+574T>C | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 10/11 | chr10 | 102618002 | |||||||
| chr10:102618005 | T | C | 263 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(260): Show |
263 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(260): 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0141 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0157 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0167 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0210 a0001c0001t0005g0080 others(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 | a0001c0001t0001g0254 a0001c0001t0017g0191 a0001c0002t0002g0001 others(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 | a0001c0001t0004g0113 a0001c0002t0002g0048 a0001c0002t0002g0059 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0112 a0001c0001t0001g0253 |
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 | a0001c0002t0002g0045 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0233 a0001c0001t0003g0181 a0001c0001t0003g0218 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0217 others(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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0002t0034g0084 | 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 | a0001c0001t0012g0237 a0001c0001t0012g0262 |
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 | a0001c0002t0034g0084 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0004g0113 | 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 | a0001c0002t0002g0037 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0014g0017 a0001c0001t0014g0018 a0001c0001t0032g0069 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0133 a0001c0001t0001g0148 others(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 | a0001c0002t0002g0026 a0001c0002t0002g0042 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0168 a0001c0001t0003g0229 a0001c0001t0003g0240 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0155 a0001c0001t0001g0163 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0155 a0001c0002t0002g0001 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0155 a0001c0002t0002g0001 others(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 | a0001c0002t0002g0037 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0155 a0001c0002t0002g0001 others(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 | a0001c0002t0002g0037 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0147 |
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 | a0001c0001t0004g0129 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0146 others(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 | |||||||
| chr10:102625641 | G | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0177 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0177 a0001c0001t0001g0212 others(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 | a0001c0001t0004g0110 a0001c0002t0002g0001 a0001c0002t0002g0002 others(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 | 110 | a0001c0001t0001g0112 a0001c0001t0001g0176 a0001c0001t0001g0177 others(107): Show |
110 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0230 others(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 | 188 | a0001c0001t0001g0112 a0001c0001t0001g0176 a0001c0001t0001g0177 others(185): Show |
188 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(185): 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 | a0001c0001t0006g0257 a0001c0001t0031g0258 |
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 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(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 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(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 | a0001c0001t0008g0022 a0001c0001t0008g0092 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0146 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0085 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0001g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366-540C>T | SUFU | ENSG00000107882.12 | transcript | ENST00000369902.8 | protein_coding | 11/11 | chr10 | 102629526 |