Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25814 |
| ensemblid | ENSG00000130638.18 |
| hgncid | 10549 |
| symbol | ATXN10 |
| name | ataxin 10 |
| refseq_nuc | NM_013236.4 |
| refseq_prot | NP_037368.1 |
| ensembl_nuc | ENST00000252934.10 |
| ensembl_prot | ENSP00000252934.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 45671834 |
| end | 45845307 |
| strand | + |
| ver | v1.2 |
| region | chr22:45671834-45845307 |
| region5000 | chr22:45666834-45850307 |
| regionname0 | ATXN10_chr22_45671834_45845307 |
| regionname5000 | ATXN10_chr22_45666834_45850307 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 475 | 314 | 83 | 44 | 141 | 10 | 34 | 112 | ATXN10_chr22_45666834_45850307 | ATXN10 | MAAPR others(470): Show |
chr22 | 45666834 | 45850307 |
| a0002 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | MAAPR others(470): Show |
chr22 | 45666834 | 45850307 |
| a0003 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | MAAPR others(470): Show |
chr22 | 45666834 | 45850307 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1425 | 314 | 83 | 44 | 141 | 10 | 34 | ATXN10_chr22_45666834_45850307 | ATXN10 | ATGGC others(1420): Show |
chr22 | 45666834 | 45850307 | ||
| a0002c0003 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | ATGGC others(1420): Show |
chr22 | 45666834 | 45850307 | ||
| a0003c0002 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | ATGGC others(1420): Show |
chr22 | 45666834 | 45850307 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3294 | 250 | 60 | 34 | 124 | 6 | 24 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0002 | 0/0 | 3294 | 30 | 5 | 5 | 13 | 3 | 4 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0003 | 0/0 | 3294 | 9 | 3 | 5 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0004 | 0/0 | 3294 | 5 | 0 | 0 | 0 | 0 | 5 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0005 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0006 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0007 | 0/0 | 3294 | 2 | 0 | 0 | 2 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0008 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0009 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0010 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0011 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0012 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0013 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0014 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0015 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0016 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0017 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0001c0001t0018 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0002c0003t0001 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| a0003c0002t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | GCCGT others(3289): Show |
chr22 | 45666834 | 45850307 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0017g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0003c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0118 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02155 | hp1 | a0001 | c0001 | t0017 | g0247 | EAS | CDX | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0071 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0185 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0300 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0239 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0299 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03225 | hp1 | a0003 | c0002 | t0001 | g0064 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0113 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0081 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0225 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0301 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0077 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19000 | hp1 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ASW | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0104 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0218 | REF | REF | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45729582 | G | A | 1 | a0003 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.886G>A | p.Asp296Asn | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/12 | 1116/3294 | 886/1428 | 296/475 | chr22 | 45729582 | |||
| chr22:45843021 | G | A | 1 | a0002 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1268G>A | p.Arg423Gln | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/12 | 1498/3294 | 1268/1428 | 423/475 | chr22 | 45843021 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45671960 | C | T | 2 | a0001c0001t0006 a0001c0001t0018 |
4 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-104C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/12 | 104 | chr22 | 45671960 | ||||||
| chr22:45671990 | C | T | 1 | a0001c0001t0017 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/12 | 74 | chr22 | 45671990 | ||||||
| chr22:45672005 | C | T | 1 | a0001c0001t0008 | 2 | HG03098.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-59C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/12 | 59 | chr22 | 45672005 | ||||||
| chr22:45672016 | C | T | 1 | a0001c0001t0016 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/12 | 48 | chr22 | 45672016 | ||||||
| chr22:45844018 | C | T | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 347 | chr22 | 45844018 | ||||||
| chr22:45844049 | A | G | 1 | a0001c0001t0005 | 3 | HG02280.hp2 HG03139.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*378A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 378 | chr22 | 45844049 | ||||||
| chr22:45844054 | C | T | 1 | a0001c0001t0003 | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*383C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 383 | chr22 | 45844054 | ||||||
| chr22:45844173 | C | T | 2 | a0001c0001t0006 a0001c0001t0014 |
4 | HG02258.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*502C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 502 | chr22 | 45844173 | ||||||
| chr22:45844210 | G | A | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(1): Show |
33 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 539 | chr22 | 45844210 | ||||||
| chr22:45844526 | T | A | 1 | a0001c0001t0011 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 855 | chr22 | 45844526 | ||||||
| chr22:45844572 | T | C | 1 | a0001c0001t0009 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 901 | chr22 | 45844572 | ||||||
| chr22:45844587 | A | T | 1 | a0001c0001t0010 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 916 | chr22 | 45844587 | ||||||
| chr22:45844615 | G | A | 1 | a0001c0001t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 944 | chr22 | 45844615 | ||||||
| chr22:45844837 | G | T | 1 | a0001c0001t0004 | 5 | HG03491.hp2 HG03492.hp2 HG03669.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1166G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 1166 | chr22 | 45844837 | ||||||
| chr22:45845211 | A | G | 1 | a0001c0001t0013 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1540A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 1540 | chr22 | 45845211 | ||||||
| chr22:45845259 | T | G | 1 | a0001c0001t0007 | 2 | NA18982.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1588T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 12/12 | 1588 | chr22 | 45845259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45672252 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+73G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672252 | |||||||
| chr22:45672264 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.116+85G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672264 | |||||||
| chr22:45672264 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.116+85G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672264 | |||||||
| chr22:45672268 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.116+89C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672268 | |||||||
| chr22:45672294 | A | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18970.hp2 NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.116+115A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672294 | |||||||
| chr22:45672311 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116+132C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672311 | |||||||
| chr22:45672575 | G | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+396G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672575 | |||||||
| chr22:45672611 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116+432G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672611 | |||||||
| chr22:45672687 | G | C | 75 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(72): Show |
75 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.116+508G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672687 | |||||||
| chr22:45672688 | C | G | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+509C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672688 | |||||||
| chr22:45672746 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116+567G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672746 | |||||||
| chr22:45672749 | C | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+570C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672749 | |||||||
| chr22:45672764 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.116+585G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672764 | |||||||
| chr22:45672814 | G | T | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+635G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672814 | |||||||
| chr22:45672823 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.116+644C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672823 | |||||||
| chr22:45672861 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.116+682C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672861 | |||||||
| chr22:45672920 | G | T | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.116+741G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672920 | |||||||
| chr22:45672947 | C | T | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+768C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45672947 | |||||||
| chr22:45673117 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.116+938C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673117 | |||||||
| chr22:45673182 | A | C | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116+1003A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673182 | |||||||
| chr22:45673229 | C | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.116+1050C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673229 | |||||||
| chr22:45673241 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116+1062T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673241 | |||||||
| chr22:45673468 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.116+1289A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673468 | |||||||
| chr22:45673536 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.116+1357C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673536 | |||||||
| chr22:45673570 | T | C | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116+1391T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673570 | |||||||
| chr22:45673666 | A | T | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+1487A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673666 | |||||||
| chr22:45673784 | C | G | 21 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(18): Show |
21 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.116+1605C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673784 | |||||||
| chr22:45673785 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116+1606G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673785 | |||||||
| chr22:45673807 | G | A | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(12): Show |
15 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+1628G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673807 | |||||||
| chr22:45673818 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.116+1639C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45673818 | |||||||
| chr22:45674106 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.116+1927A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674106 | |||||||
| chr22:45674245 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.116+2066G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674245 | |||||||
| chr22:45674261 | G | C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+2082G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674261 | |||||||
| chr22:45674369 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.116+2190C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674369 | |||||||
| chr22:45674603 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0004g0140 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.116+2424T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674603 | |||||||
| chr22:45674615 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116+2436C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674615 | |||||||
| chr22:45674617 | A | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+2438A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674617 | |||||||
| chr22:45674799 | C | A | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+2620C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674799 | |||||||
| chr22:45674928 | G | T | 3 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0018g0118 |
3 | HG01884.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.116+2749G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674928 | |||||||
| chr22:45674970 | C | T | 29 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.116+2791C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45674970 | |||||||
| chr22:45675087 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.116+2908A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675087 | |||||||
| chr22:45675130 | A | G | 29 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.116+2951A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675130 | |||||||
| chr22:45675136 | G | A | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+2957G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675136 | |||||||
| chr22:45675420 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.116+3241T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675420 | |||||||
| chr22:45675446 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.116+3267C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675446 | |||||||
| chr22:45675456 | G | T | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.116+3277G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675456 | |||||||
| chr22:45675512 | C | G | 10 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+3333C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675512 | |||||||
| chr22:45675586 | G | C | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.116+3407G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675586 | |||||||
| chr22:45675808 | T | G | 75 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.116+3629T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675808 | |||||||
| chr22:45675888 | T | C | 12 | a0001c0001t0001g0130 a0001c0001t0001g0210 a0001c0001t0001g0211 others(9): Show |
12 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+3709T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675888 | |||||||
| chr22:45675964 | ACTTTTTG others(6): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+3786_116+3798d others(15): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45675964 | |||||||
| chr22:45676283 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4104G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676283 | |||||||
| chr22:45676319 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG03490.hp1 others(15): Show |
intron_variant | MODIFIER | c.116+4140G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676319 | |||||||
| chr22:45676319 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.116+4140G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676319 | |||||||
| chr22:45676386 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.116+4207A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676386 | |||||||
| chr22:45676485 | G | GT | 17 | a0001c0001t0001g0054 a0001c0001t0001g0124 a0001c0001t0001g0204 others(14): Show |
17 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+4319dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45676485 | ||||||
| chr22:45676573 | G | A | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116+4394G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676573 | |||||||
| chr22:45676593 | C | T | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116+4414C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676593 | |||||||
| chr22:45676806 | G | A | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116+4627G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676806 | |||||||
| chr22:45676806 | G | T | 4 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+4627G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45676806 | |||||||
| chr22:45677008 | AT | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.116+4833delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45677008 | ||||||
| chr22:45677027 | C | T | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.116+4848C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45677027 | |||||||
| chr22:45677503 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.116+5324G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45677503 | |||||||
| chr22:45677515 | TA | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0052 others(43): Show |
46 | HG00099.hp1 HG00735.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.116+5350delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45677515 | ||||||
| chr22:45677646 | A | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+5467A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45677646 | |||||||
| chr22:45677682 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116+5503A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45677682 | |||||||
| chr22:45677724 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.116+5545C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45677724 | |||||||
| chr22:45678303 | T | C | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+6124T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678303 | |||||||
| chr22:45678365 | T | A | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+6186T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678365 | |||||||
| chr22:45678378 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.116+6199G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678378 | |||||||
| chr22:45678405 | T | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(12): Show |
15 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+6226T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678405 | |||||||
| chr22:45678570 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.116+6391C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678570 | |||||||
| chr22:45678644 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.116+6465G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678644 | |||||||
| chr22:45678765 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116+6586C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678765 | |||||||
| chr22:45678824 | T | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(12): Show |
15 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+6645T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45678824 | |||||||
| chr22:45679096 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.116+6917C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679096 | |||||||
| chr22:45679129 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+6950T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679129 | |||||||
| chr22:45679249 | G | A | 55 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(52): Show |
55 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.116+7070G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679249 | |||||||
| chr22:45679251 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+7072G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679251 | |||||||
| chr22:45679492 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.116+7313G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679492 | |||||||
| chr22:45679543 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.116+7364C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679543 | |||||||
| chr22:45679587 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.116+7408C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679587 | |||||||
| chr22:45679605 | C | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+7426C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679605 | |||||||
| chr22:45679692 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.116+7513G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679692 | |||||||
| chr22:45679738 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116+7559A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679738 | |||||||
| chr22:45679751 | A | C | 1 | a0001c0001t0001g0017 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.116+7572A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679751 | |||||||
| chr22:45679915 | C | T | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+7736C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679915 | |||||||
| chr22:45679942 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.116+7763A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45679942 | |||||||
| chr22:45680151 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.116+7972C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680151 | |||||||
| chr22:45680382 | A | G | 32 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.116+8203A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680382 | |||||||
| chr22:45680482 | A | G | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+8303A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680482 | |||||||
| chr22:45680629 | A | AT | 10 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0067 others(7): Show |
10 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+8464dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45680629 | ||||||
| chr22:45680629 | AT | A | 9 | a0001c0001t0001g0124 a0001c0001t0002g0090 a0001c0001t0003g0122 others(6): Show |
9 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+8464delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45680629 | ||||||
| chr22:45680666 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+8487G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680666 | |||||||
| chr22:45680738 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.116+8559A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680738 | |||||||
| chr22:45680792 | C | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+8613C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45680792 | |||||||
| chr22:45681033 | C | T | 10 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.117-8679C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681033 | |||||||
| chr22:45681191 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.117-8521C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681191 | |||||||
| chr22:45681355 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-8357G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681355 | |||||||
| chr22:45681376 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01943.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117-8336C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681376 | |||||||
| chr22:45681429 | G | A | 9 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | NA18612.hp2 NA18942.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-8283G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681429 | |||||||
| chr22:45681447 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117-8265C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681447 | |||||||
| chr22:45681687 | C | T | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0005g0291 others(1): Show |
4 | HG01891.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-8025C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681687 | |||||||
| chr22:45681689 | T | G | 2 | a0001c0001t0001g0265 a0001c0001t0011g0136 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-8023T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681689 | |||||||
| chr22:45681692 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-8020A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681692 | |||||||
| chr22:45681709 | A | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0281 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.117-8003A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681709 | |||||||
| chr22:45681724 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.117-7988A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681724 | |||||||
| chr22:45681845 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.117-7867C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681845 | |||||||
| chr22:45681941 | C | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117-7771C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45681941 | |||||||
| chr22:45682391 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.117-7321C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682391 | |||||||
| chr22:45682439 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117-7273C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682439 | |||||||
| chr22:45682479 | T | A | 2 | a0001c0001t0001g0265 a0001c0001t0011g0136 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-7233T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682479 | |||||||
| chr22:45682483 | T | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.117-7229T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682483 | |||||||
| chr22:45682484 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.117-7228T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682484 | |||||||
| chr22:45682498 | CAG | C | 28 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0111 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.117-7213_117-7212d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682498 | |||||||
| chr22:45682635 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.117-7077A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682635 | |||||||
| chr22:45682669 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.117-7043A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682669 | |||||||
| chr22:45682701 | G | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0274 |
3 | HG01243.hp2 HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.117-7011G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682701 | |||||||
| chr22:45682788 | C | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0002g0213 |
3 | HG02965.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117-6924C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682788 | |||||||
| chr22:45682833 | A | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.117-6879A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45682833 | |||||||
| chr22:45683191 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-6521T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683191 | |||||||
| chr22:45683259 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117-6453C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683259 | |||||||
| chr22:45683335 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.117-6377A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683335 | |||||||
| chr22:45683374 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117-6338C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683374 | |||||||
| chr22:45683413 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0050 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.117-6299T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683413 | |||||||
| chr22:45683608 | C | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(5): Show |
8 | HG00408.hp2 HG00597.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-6104C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683608 | |||||||
| chr22:45683942 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.117-5770C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45683942 | |||||||
| chr22:45684035 | T | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-5677T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684035 | |||||||
| chr22:45684137 | G | GT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00741.hp2 HG02738.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-5561dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45684137 | ||||||
| chr22:45684137 | GT | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.117-5561delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45684137 | ||||||
| chr22:45684253 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-5459G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684253 | |||||||
| chr22:45684280 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-5432G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684280 | |||||||
| chr22:45684350 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.117-5362T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684350 | |||||||
| chr22:45684371 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-5341G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684371 | |||||||
| chr22:45684384 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.117-5328C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684384 | |||||||
| chr22:45684392 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0011g0136 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-5320G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684392 | |||||||
| chr22:45684404 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG02145.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-5308A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684404 | |||||||
| chr22:45684441 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117-5271T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684441 | |||||||
| chr22:45684500 | G | A | 82 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(79): Show |
82 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.117-5212G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684500 | |||||||
| chr22:45684603 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-5109C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684603 | |||||||
| chr22:45684629 | T | C | 10 | a0001c0001t0001g0124 a0001c0001t0002g0203 a0001c0001t0003g0122 others(7): Show |
10 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.117-5083T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684629 | |||||||
| chr22:45684691 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.117-5021A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684691 | |||||||
| chr22:45684740 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.117-4972C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684740 | |||||||
| chr22:45684799 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.117-4913C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684799 | |||||||
| chr22:45684920 | G | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.117-4792G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684920 | |||||||
| chr22:45684922 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.117-4790G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684922 | |||||||
| chr22:45684972 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.117-4740C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45684972 | |||||||
| chr22:45685095 | CT | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.117-4603delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45685095 | ||||||
| chr22:45685227 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.117-4485A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45685227 | |||||||
| chr22:45685317 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.117-4395T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45685317 | |||||||
| chr22:45685389 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-4323G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45685389 | |||||||
| chr22:45685739 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-3973G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45685739 | |||||||
| chr22:45685772 | CATATT | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-3934_117-3930d others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45685772 | ||||||
| chr22:45685923 | G | GTTA | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0274 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-3787_117-3785d others(5): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45685923 | ||||||
| chr22:45686096 | G | A | 32 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.117-3616G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686096 | |||||||
| chr22:45686144 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-3568A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686144 | |||||||
| chr22:45686150 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117-3562A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686150 | |||||||
| chr22:45686261 | GCAAA | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(1): Show |
4 | HG02717.hp2 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-3448_117-3445d others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45686261 | ||||||
| chr22:45686386 | G | A | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.117-3326G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686386 | |||||||
| chr22:45686591 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117-3121G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686591 | |||||||
| chr22:45686773 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-2939C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686773 | |||||||
| chr22:45686818 | CA | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.117-2877delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45686818 | ||||||
| chr22:45686940 | G | A | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117-2772G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45686940 | |||||||
| chr22:45687059 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117-2653T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687059 | |||||||
| chr22:45687144 | G | A | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-2568G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687144 | |||||||
| chr22:45687243 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.117-2469T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687243 | |||||||
| chr22:45687434 | A | G | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.117-2278A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687434 | |||||||
| chr22:45687695 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.117-2017A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687695 | |||||||
| chr22:45687761 | TAAG | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0056 others(1): Show |
4 | NA18988.hp1 NA18988.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-1948_117-1946d others(5): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 45687761 | ||||||
| chr22:45687858 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.117-1854A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687858 | |||||||
| chr22:45687902 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117-1810C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687902 | |||||||
| chr22:45687914 | G | A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0282 a0001c0001t0001g0283 others(3): Show |
6 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-1798G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687914 | |||||||
| chr22:45687926 | G | A | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-1786G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45687926 | |||||||
| chr22:45688053 | G | A | 7 | a0001c0001t0001g0143 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.117-1659G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688053 | |||||||
| chr22:45688150 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.117-1562T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688150 | |||||||
| chr22:45688312 | A | G | 16 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(13): Show |
16 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.117-1400A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688312 | |||||||
| chr22:45688460 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.117-1252G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688460 | |||||||
| chr22:45688466 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.117-1246C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688466 | |||||||
| chr22:45688503 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117-1209C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688503 | |||||||
| chr22:45688505 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0014g0077 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117-1207A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688505 | |||||||
| chr22:45688515 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-1197C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688515 | |||||||
| chr22:45688580 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.117-1132G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688580 | |||||||
| chr22:45688858 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.117-854C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688858 | |||||||
| chr22:45688904 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-808A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688904 | |||||||
| chr22:45688943 | T | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-769T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688943 | |||||||
| chr22:45688948 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0004g0112 a0001c0001t0004g0113 |
3 | HG03491.hp2 HG03492.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.117-764G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45688948 | |||||||
| chr22:45689060 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.117-652G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45689060 | |||||||
| chr22:45689154 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.117-558C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45689154 | |||||||
| chr22:45689492 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117-220G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 1/11 | chr22 | 45689492 | |||||||
| chr22:45689915 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.308+12C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45689915 | |||||||
| chr22:45690279 | G | GA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0061 others(5): Show |
8 | HG00738.hp2 HG01099.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.308+393dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 45690279 | ||||||
| chr22:45690280 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.308+377A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45690280 | |||||||
| chr22:45690375 | C | A | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.308+472C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45690375 | |||||||
| chr22:45690382 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.308+479A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45690382 | |||||||
| chr22:45690691 | C | T | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.308+788C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45690691 | |||||||
| chr22:45690896 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308+993T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45690896 | |||||||
| chr22:45691230 | C | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.308+1327C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691230 | |||||||
| chr22:45691239 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.308+1336C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691239 | |||||||
| chr22:45691267 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.308+1364C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691267 | |||||||
| chr22:45691290 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0139 others(63): Show |
67 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.308+1387G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691290 | |||||||
| chr22:45691341 | G | A | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+1438G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691341 | |||||||
| chr22:45691358 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.308+1455C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691358 | |||||||
| chr22:45691452 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.309-1544T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691452 | |||||||
| chr22:45691749 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.309-1247T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691749 | |||||||
| chr22:45691873 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.309-1123A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691873 | |||||||
| chr22:45691888 | G | T | 22 | a0001c0001t0001g0214 a0001c0001t0001g0265 a0001c0001t0001g0270 others(19): Show |
22 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.309-1108G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691888 | |||||||
| chr22:45691940 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.309-1056G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45691940 | |||||||
| chr22:45692069 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.309-927G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692069 | |||||||
| chr22:45692111 | T | G | 1 | a0001c0001t0005g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.309-885T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692111 | |||||||
| chr22:45692239 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.309-757T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692239 | |||||||
| chr22:45692304 | G | C | 64 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(61): Show |
64 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.309-692G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692304 | |||||||
| chr22:45692584 | A | C | 1 | a0001c0001t0012g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309-412A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692584 | |||||||
| chr22:45692592 | A | G | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-404A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692592 | |||||||
| chr22:45692599 | T | C | 1 | a0001c0001t0005g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.309-397T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692599 | |||||||
| chr22:45692603 | A | T | 2 | a0001c0001t0007g0205 a0001c0001t0007g0206 |
2 | NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.309-393A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 2/11 | chr22 | 45692603 | |||||||
| chr22:45693097 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+19C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693097 | |||||||
| chr22:45693098 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+20A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693098 | |||||||
| chr22:45693227 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+149A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693227 | |||||||
| chr22:45693374 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+296G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693374 | |||||||
| chr22:45693464 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.391+386C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693464 | |||||||
| chr22:45693554 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.391+476A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693554 | |||||||
| chr22:45693615 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391+537C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693615 | |||||||
| chr22:45693625 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+547A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693625 | |||||||
| chr22:45693735 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.391+657A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693735 | |||||||
| chr22:45693760 | G | A | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.391+682G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693760 | |||||||
| chr22:45693973 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.391+895A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693973 | |||||||
| chr22:45693995 | T | C | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.391+917T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45693995 | |||||||
| chr22:45694090 | T | A | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.391+1012T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694090 | |||||||
| chr22:45694126 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.391+1048G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694126 | |||||||
| chr22:45694160 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+1082A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694160 | |||||||
| chr22:45694329 | A | C | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391+1251A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694329 | |||||||
| chr22:45694371 | G | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0263 others(2): Show |
5 | HG00099.hp1 HG01070.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+1293G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694371 | |||||||
| chr22:45694381 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+1303G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694381 | |||||||
| chr22:45694382 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+1304T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694382 | |||||||
| chr22:45694431 | T | G | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.391+1353T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694431 | |||||||
| chr22:45694493 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391+1415A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694493 | |||||||
| chr22:45694534 | C | G | 52 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(49): Show |
52 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.391+1456C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694534 | |||||||
| chr22:45694670 | T | A | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+1592T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694670 | |||||||
| chr22:45694940 | C | CA | 85 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(82): Show |
85 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.391+1888dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45694940 | ||||||
| chr22:45694940 | C | CAA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0067 others(12): Show |
15 | HG00423.hp2 HG01884.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.391+1887_391+1888d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45694940 | ||||||
| chr22:45694940 | CA | C | 13 | a0001c0001t0001g0124 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
13 | HG00735.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.391+1888delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45694940 | ||||||
| chr22:45694951 | A | C | 4 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1873A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694951 | |||||||
| chr22:45694958 | A | C | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+1880A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694958 | |||||||
| chr22:45694967 | C | A | 21 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.391+1889C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694967 | |||||||
| chr22:45694972 | C | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1894C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45694972 | |||||||
| chr22:45695140 | C | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+2062C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695140 | |||||||
| chr22:45695180 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.391+2102C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695180 | |||||||
| chr22:45695216 | G | C | 89 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(86): Show |
89 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.391+2138G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695216 | |||||||
| chr22:45695217 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.391+2139G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695217 | |||||||
| chr22:45695241 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391+2163A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695241 | |||||||
| chr22:45695244 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391+2166C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695244 | |||||||
| chr22:45695324 | C | CA | 7 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0197 others(4): Show |
7 | HG00423.hp1 HG01981.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+2263dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45695324 | ||||||
| chr22:45695366 | C | G | 35 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(32): Show |
35 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.391+2288C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695366 | |||||||
| chr22:45695494 | C | CT | 179 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0047 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.391+2429dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45695494 | ||||||
| chr22:45695501 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.391+2423T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695501 | |||||||
| chr22:45695553 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.391+2475G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695553 | |||||||
| chr22:45695601 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+2523C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695601 | |||||||
| chr22:45695646 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.391+2568G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45695646 | |||||||
| chr22:45695751 | C | CA | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(2): Show |
5 | HG02717.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+2676dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45695751 | ||||||
| chr22:45696011 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.391+2933T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696011 | |||||||
| chr22:45696156 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391+3078A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696156 | |||||||
| chr22:45696186 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+3108T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696186 | |||||||
| chr22:45696251 | C | T | 11 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+3173C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696251 | |||||||
| chr22:45696367 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.391+3289G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696367 | |||||||
| chr22:45696630 | A | T | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+3552A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696630 | |||||||
| chr22:45696906 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.392-3376G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45696906 | |||||||
| chr22:45697025 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.392-3257G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697025 | |||||||
| chr22:45697179 | G | T | 14 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(11): Show |
14 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.392-3103G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697179 | |||||||
| chr22:45697291 | C | T | 13 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.392-2991C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697291 | |||||||
| chr22:45697329 | T | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-2953T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697329 | |||||||
| chr22:45697341 | G | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-2941G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697341 | |||||||
| chr22:45697394 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.392-2888G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697394 | |||||||
| chr22:45697430 | C | T | 48 | a0001c0001t0001g0143 a0001c0001t0001g0216 a0001c0001t0001g0217 others(45): Show |
48 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.392-2852C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697430 | |||||||
| chr22:45697431 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.392-2851G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697431 | |||||||
| chr22:45697715 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0273 |
2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.392-2567C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697715 | |||||||
| chr22:45697755 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.392-2527C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697755 | |||||||
| chr22:45697759 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.392-2523C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697759 | |||||||
| chr22:45697792 | A | G | 7 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(4): Show |
7 | HG00738.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-2490A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697792 | |||||||
| chr22:45697841 | A | G | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.392-2441A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45697841 | |||||||
| chr22:45698083 | T | A | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-2199T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698083 | |||||||
| chr22:45698083 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.392-2199T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698083 | |||||||
| chr22:45698143 | T | C | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-2139T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698143 | |||||||
| chr22:45698153 | G | A | 2 | a0001c0001t0007g0205 a0001c0001t0007g0206 |
2 | NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.392-2129G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698153 | |||||||
| chr22:45698228 | A | G | 1 | a0001c0001t0006g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.392-2054A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698228 | |||||||
| chr22:45698603 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.392-1679T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698603 | |||||||
| chr22:45698645 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.392-1637A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698645 | |||||||
| chr22:45698734 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.392-1548C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698734 | |||||||
| chr22:45698994 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-1288G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45698994 | |||||||
| chr22:45699106 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.392-1176G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699106 | |||||||
| chr22:45699369 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.392-913G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699369 | |||||||
| chr22:45699467 | C | CT | 76 | a0001c0001t0001g0014 a0001c0001t0001g0142 a0001c0001t0001g0144 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.392-804dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699467 | ||||||
| chr22:45699467 | CT | C | 17 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0242 others(14): Show |
17 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.392-804delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699467 | ||||||
| chr22:45699490 | C | CT | 26 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0023 others(23): Show |
26 | HG00642.hp1 HG00738.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.392-773dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699490 | ||||||
| chr22:45699490 | C | CTT | 7 | a0001c0001t0001g0173 a0001c0001t0003g0125 a0001c0001t0003g0126 others(4): Show |
7 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-774_392-773dup others(2): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699490 | ||||||
| chr22:45699490 | C | CTTT | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-775_392-773dup others(3): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699490 | ||||||
| chr22:45699533 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.392-749C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699533 | |||||||
| chr22:45699643 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0011g0136 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.392-639C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699643 | |||||||
| chr22:45699840 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-442C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699840 | |||||||
| chr22:45699847 | A | AT | 19 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0070 others(16): Show |
19 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.392-418dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699847 | ||||||
| chr22:45699847 | AT | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0065 others(8): Show |
11 | HG01168.hp2 HG01891.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.392-418delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | 45699847 | ||||||
| chr22:45699908 | G | A | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-374G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699908 | |||||||
| chr22:45699962 | C | T | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-320C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45699962 | |||||||
| chr22:45700059 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.392-223G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700059 | |||||||
| chr22:45700063 | T | C | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-219T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700063 | |||||||
| chr22:45700117 | A | G | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(36): Show |
39 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.392-165A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700117 | |||||||
| chr22:45700142 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.392-140C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700142 | |||||||
| chr22:45700152 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.392-130C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700152 | |||||||
| chr22:45700186 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.392-96T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 3/11 | chr22 | 45700186 | |||||||
| chr22:45700855 | TG | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+479delG | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | 45700855 | ||||||
| chr22:45700982 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0001g0241 a0001c0001t0004g0140 others(1): Show |
4 | HG02109.hp1 HG03669.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+604A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45700982 | |||||||
| chr22:45701092 | T | C | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.488+714T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701092 | |||||||
| chr22:45701123 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+745T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701123 | |||||||
| chr22:45701201 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488+823C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701201 | |||||||
| chr22:45701242 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0139 others(66): Show |
70 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.488+864T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701242 | |||||||
| chr22:45701423 | C | A | 1 | a0001c0001t0001g0311 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.488+1045C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701423 | |||||||
| chr22:45701605 | G | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0080 others(3): Show |
6 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-1084G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701605 | |||||||
| chr22:45701704 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.489-985C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701704 | |||||||
| chr22:45701764 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.489-925G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45701764 | |||||||
| chr22:45702189 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.489-500G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702189 | |||||||
| chr22:45702241 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.489-448A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702241 | |||||||
| chr22:45702257 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.489-432C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702257 | |||||||
| chr22:45702282 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0101 |
2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.489-407T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702282 | |||||||
| chr22:45702284 | T | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0101 |
2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.489-405T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702284 | |||||||
| chr22:45702441 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.489-248G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702441 | |||||||
| chr22:45702582 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.489-107C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 4/11 | chr22 | 45702582 | |||||||
| chr22:45702882 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.647+35G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45702882 | |||||||
| chr22:45703205 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.647+358C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703205 | |||||||
| chr22:45703260 | C | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0134 a0001c0001t0002g0135 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+413C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703260 | |||||||
| chr22:45703291 | A | G | 16 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.647+444A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703291 | |||||||
| chr22:45703346 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+499G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703346 | |||||||
| chr22:45703403 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.647+556A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703403 | |||||||
| chr22:45703733 | A | G | 16 | a0001c0001t0001g0034 a0001c0001t0001g0124 a0001c0001t0001g0130 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.647+886A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703733 | |||||||
| chr22:45703837 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 |
3 | NA18989.hp1 NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.647+990C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703837 | |||||||
| chr22:45703943 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.647+1096G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703943 | |||||||
| chr22:45703948 | C | CA | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+1103dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45703948 | ||||||
| chr22:45703954 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.647+1107A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45703954 | |||||||
| chr22:45704125 | C | CT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.647+1293dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45704125 | ||||||
| chr22:45704125 | CT | C | 31 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.647+1293delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45704125 | ||||||
| chr22:45704310 | T | TA | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0006g0087 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.647+1475dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45704310 | ||||||
| chr22:45704420 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.647+1573G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45704420 | |||||||
| chr22:45704456 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0012g0081 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.647+1609G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45704456 | |||||||
| chr22:45704499 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647+1652C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45704499 | |||||||
| chr22:45704681 | G | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0313 |
3 | HG02145.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.647+1834G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45704681 | |||||||
| chr22:45704808 | A | C | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+1961A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45704808 | |||||||
| chr22:45705105 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+2258A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705105 | |||||||
| chr22:45705156 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.647+2309C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705156 | |||||||
| chr22:45705169 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.647+2322G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705169 | |||||||
| chr22:45705183 | A | C | 15 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(12): Show |
15 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.647+2336A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705183 | |||||||
| chr22:45705190 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.647+2343A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705190 | |||||||
| chr22:45705226 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.647+2379T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705226 | |||||||
| chr22:45705440 | G | GT | 16 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0130 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.647+2604dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45705440 | ||||||
| chr22:45705550 | A | G | 9 | a0001c0001t0001g0124 a0001c0001t0002g0203 a0001c0001t0003g0122 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.647+2703A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705550 | |||||||
| chr22:45705593 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0002g0213 |
3 | HG02965.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.647+2746C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705593 | |||||||
| chr22:45705610 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.647+2763A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705610 | |||||||
| chr22:45705737 | A | G | 15 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0002g0131 others(12): Show |
15 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.647+2890A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705737 | |||||||
| chr22:45705845 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0241 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.647+2998G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705845 | |||||||
| chr22:45705926 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+3079C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705926 | |||||||
| chr22:45705936 | C | T | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.647+3089C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45705936 | |||||||
| chr22:45706103 | C | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0002g0213 |
3 | HG02965.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.647+3256C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45706103 | |||||||
| chr22:45706437 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.647+3590G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45706437 | |||||||
| chr22:45706506 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.647+3659A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45706506 | |||||||
| chr22:45706639 | C | T | 9 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(6): Show |
9 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.647+3792C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45706639 | |||||||
| chr22:45706698 | G | GTTTATTT others(23): Show |
5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+3854_647+3855i others(32): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45706698 | ||||||
| chr22:45706919 | T | G | 9 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(6): Show |
9 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.647+4072T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45706919 | |||||||
| chr22:45707044 | CAT | C | 21 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.647+4198_647+4199d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707044 | |||||||
| chr22:45707067 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.647+4220T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707067 | |||||||
| chr22:45707322 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.647+4475G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707322 | |||||||
| chr22:45707476 | C | A | 10 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.647+4629C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707476 | |||||||
| chr22:45707552 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.647+4705G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707552 | |||||||
| chr22:45707568 | C | T | 29 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.647+4721C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707568 | |||||||
| chr22:45707640 | A | G | 9 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(6): Show |
9 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.647+4793A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707640 | |||||||
| chr22:45707650 | G | GATATA | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+4819_647+4823d others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45707650 | ||||||
| chr22:45707650 | G | GATATAAT others(3): Show |
1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.647+4814_647+4823d others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45707650 | ||||||
| chr22:45707962 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.647+5115A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45707962 | |||||||
| chr22:45708028 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+5181C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708028 | |||||||
| chr22:45708118 | T | C | 10 | a0001c0001t0001g0124 a0001c0001t0002g0203 a0001c0001t0003g0122 others(7): Show |
10 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.647+5271T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708118 | |||||||
| chr22:45708175 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+5328T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708175 | |||||||
| chr22:45708201 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01943.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.647+5354A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708201 | |||||||
| chr22:45708290 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.647+5443G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708290 | |||||||
| chr22:45708426 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.647+5579T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708426 | |||||||
| chr22:45708497 | C | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.647+5650C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708497 | |||||||
| chr22:45708553 | T | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG00621.hp2 HG01943.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+5706T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708553 | |||||||
| chr22:45708891 | T | C | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.647+6044T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45708891 | |||||||
| chr22:45709182 | C | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0214 a0001c0001t0002g0131 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.647+6335C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709182 | |||||||
| chr22:45709185 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.647+6338G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709185 | |||||||
| chr22:45709277 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.647+6430T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709277 | |||||||
| chr22:45709297 | A | G | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.647+6450A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709297 | |||||||
| chr22:45709377 | G | C | 32 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.647+6530G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709377 | |||||||
| chr22:45709479 | CTGTCTCA others(4): Show |
C | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.647+6641_647+6651d others(13): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45709479 | ||||||
| chr22:45709778 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0175 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.647+6931G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709778 | |||||||
| chr22:45709870 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0190 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.647+7023A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709870 | |||||||
| chr22:45709993 | A | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0214 a0001c0001t0002g0131 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.647+7146A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45709993 | |||||||
| chr22:45710032 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+7185C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710032 | |||||||
| chr22:45710250 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0070 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.647+7403A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710250 | |||||||
| chr22:45710261 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.647+7414C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710261 | |||||||
| chr22:45710426 | T | C | 10 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.647+7579T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710426 | |||||||
| chr22:45710437 | G | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.647+7590G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710437 | |||||||
| chr22:45710444 | C | T | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.647+7597C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710444 | |||||||
| chr22:45710495 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.647+7648C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710495 | |||||||
| chr22:45710535 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.647+7688T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710535 | |||||||
| chr22:45710554 | C | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.647+7707C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710554 | |||||||
| chr22:45710559 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.647+7712T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710559 | |||||||
| chr22:45710709 | A | G | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.648-7704A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710709 | |||||||
| chr22:45710794 | C | A | 62 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(59): Show |
62 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.648-7619C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710794 | |||||||
| chr22:45710915 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-7498A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710915 | |||||||
| chr22:45710977 | G | A | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.648-7436G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45710977 | |||||||
| chr22:45711016 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.648-7397C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711016 | |||||||
| chr22:45711034 | A | G | 32 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.648-7379A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711034 | |||||||
| chr22:45711198 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.648-7215G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711198 | |||||||
| chr22:45711225 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.648-7188G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711225 | |||||||
| chr22:45711250 | GA | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0086 others(4): Show |
7 | HG01099.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.648-7153delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45711250 | ||||||
| chr22:45711286 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.648-7127A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711286 | |||||||
| chr22:45711297 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.648-7116C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711297 | |||||||
| chr22:45711548 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.648-6865G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711548 | |||||||
| chr22:45711628 | G | A | 77 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0142 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.648-6785G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711628 | |||||||
| chr22:45712028 | C | T | 1 | a0002c0003t0001g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.648-6385C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712028 | |||||||
| chr22:45712344 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
63 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.648-6069C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712344 | |||||||
| chr22:45712478 | G | A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.648-5935G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712478 | |||||||
| chr22:45712489 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0052 |
3 | HG00741.hp2 HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.648-5924G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712489 | |||||||
| chr22:45712551 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.648-5862C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712551 | |||||||
| chr22:45712599 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0273 |
3 | HG03195.hp2 NA18944.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.648-5814C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712599 | |||||||
| chr22:45712687 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0281 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.648-5726A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45712687 | |||||||
| chr22:45713011 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648-5402A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713011 | |||||||
| chr22:45713076 | C | A | 1 | a0001c0001t0004g0244 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.648-5337C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713076 | |||||||
| chr22:45713506 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.648-4907C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713506 | |||||||
| chr22:45713786 | A | G | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.648-4627A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713786 | |||||||
| chr22:45713940 | G | A | 4 | a0001c0001t0001g0281 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG02451.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-4473G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713940 | |||||||
| chr22:45713983 | A | G | 3 | a0001c0001t0008g0299 a0001c0001t0008g0301 a0001c0001t0016g0300 |
3 | HG02723.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.648-4430A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45713983 | |||||||
| chr22:45714243 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.648-4170A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45714243 | |||||||
| chr22:45714410 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-4003C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45714410 | |||||||
| chr22:45714467 | A | G | 13 | a0001c0001t0001g0124 a0001c0001t0001g0270 a0001c0001t0003g0122 others(10): Show |
13 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.648-3946A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45714467 | |||||||
| chr22:45714996 | C | G | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.648-3417C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45714996 | |||||||
| chr22:45714997 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.648-3416T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45714997 | |||||||
| chr22:45715098 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.648-3315C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715098 | |||||||
| chr22:45715162 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.648-3251G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715162 | |||||||
| chr22:45715277 | TA | T | 75 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.648-3135delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715277 | |||||||
| chr22:45715558 | G | C | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.648-2855G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715558 | |||||||
| chr22:45715562 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.648-2851T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715562 | |||||||
| chr22:45715895 | T | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0214 a0001c0001t0002g0131 others(5): Show |
8 | HG02572.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.648-2518T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715895 | |||||||
| chr22:45716325 | C | CT | 24 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0044 others(21): Show |
24 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.648-2070dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45716325 | ||||||
| chr22:45716365 | C | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.648-2048C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716365 | |||||||
| chr22:45716508 | TTG | T | 8 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1899_648-1898d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 45716508 | ||||||
| chr22:45716527 | A | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.648-1886A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716527 | |||||||
| chr22:45716545 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.648-1868G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716545 | |||||||
| chr22:45716645 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.648-1768T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716645 | |||||||
| chr22:45716695 | G | A | 50 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(47): Show |
50 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.648-1718G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716695 | |||||||
| chr22:45716751 | T | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
2 | NA19004.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.648-1662T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716751 | |||||||
| chr22:45716770 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0051 others(1): Show |
4 | NA18956.hp2 NA18969.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-1643A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45716770 | |||||||
| chr22:45717082 | C | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.648-1331C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717082 | |||||||
| chr22:45717172 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.648-1241G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717172 | |||||||
| chr22:45717299 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(7): Show |
10 | HG00423.hp2 NA18954.hp2 NA18978.hp2 others(7): Show |
intron_variant | MODIFIER | c.648-1114T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717299 | |||||||
| chr22:45717344 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.648-1069C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717344 | |||||||
| chr22:45717509 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.648-904A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717509 | |||||||
| chr22:45717831 | G | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.648-582G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45717831 | |||||||
| chr22:45718133 | C | T | 2 | a0001c0001t0007g0205 a0001c0001t0007g0206 |
2 | NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.648-280C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45718133 | |||||||
| chr22:45718267 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.648-146C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45718267 | |||||||
| chr22:45718364 | C | T | 59 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(56): Show |
59 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.648-49C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45718364 | |||||||
| chr22:45718369 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.648-44A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45718369 | |||||||
| chr22:45718518 | G | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
167 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.728+25G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45718518 | |||||||
| chr22:45718615 | G | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.728+122G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45718615 | |||||||
| chr22:45718663 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.728+170G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45718663 | |||||||
| chr22:45718917 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0236 others(1): Show |
4 | HG03942.hp2 NA18988.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+424G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45718917 | |||||||
| chr22:45718958 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.728+465T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45718958 | |||||||
| chr22:45719039 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(1): Show |
4 | HG02717.hp2 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+546G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719039 | |||||||
| chr22:45719069 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.728+576A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719069 | |||||||
| chr22:45719524 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.728+1031G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719524 | |||||||
| chr22:45719555 | A | AT | 14 | a0001c0001t0001g0151 a0001c0001t0001g0265 a0001c0001t0001g0288 others(11): Show |
14 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.728+1075dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45719555 | ||||||
| chr22:45719555 | AT | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.728+1075delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45719555 | ||||||
| chr22:45719623 | A | G | 4 | a0001c0001t0002g0099 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
4 | HG00408.hp1 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+1130A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719623 | |||||||
| chr22:45719667 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.728+1174T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719667 | |||||||
| chr22:45719673 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.728+1180G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719673 | |||||||
| chr22:45719710 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.728+1217A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719710 | |||||||
| chr22:45719850 | A | G | 31 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+1357A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45719850 | |||||||
| chr22:45720090 | T | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.728+1597T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45720090 | |||||||
| chr22:45720392 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+1899T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45720392 | |||||||
| chr22:45720403 | C | T | 4 | a0001c0001t0006g0087 a0001c0001t0006g0119 a0001c0001t0006g0120 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+1910C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45720403 | |||||||
| chr22:45720568 | G | C | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.728+2075G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45720568 | |||||||
| chr22:45720601 | A | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.728+2108A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45720601 | |||||||
| chr22:45721322 | G | A | 8 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.728+2829G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721322 | |||||||
| chr22:45721471 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0002g0046 |
3 | NA18988.hp1 NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.728+2978G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721471 | |||||||
| chr22:45721483 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.728+2990C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721483 | |||||||
| chr22:45721693 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.728+3200T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721693 | |||||||
| chr22:45721773 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0139 others(66): Show |
70 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.728+3280A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721773 | |||||||
| chr22:45721775 | T | C | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.728+3282T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721775 | |||||||
| chr22:45721807 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.728+3314C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721807 | |||||||
| chr22:45721919 | A | AAAAAC | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0121 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+3448_728+3452d others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45721919 | ||||||
| chr22:45721919 | AAAAACAA others(3): Show |
A | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.728+3443_728+3452d others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45721919 | ||||||
| chr22:45721944 | C | T | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+3451C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721944 | |||||||
| chr22:45721963 | G | A | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.728+3470G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45721963 | |||||||
| chr22:45722314 | A | T | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.728+3821A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722314 | |||||||
| chr22:45722352 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.728+3859C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722352 | |||||||
| chr22:45722387 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0002g0095 a0001c0001t0002g0100 others(1): Show |
4 | HG00140.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3894A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722387 | |||||||
| chr22:45722433 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.728+3940C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722433 | |||||||
| chr22:45722491 | T | C | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.728+3998T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722491 | |||||||
| chr22:45722497 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.728+4004T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722497 | |||||||
| chr22:45722561 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.728+4068T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722561 | |||||||
| chr22:45722668 | A | G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+4175A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722668 | |||||||
| chr22:45722678 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.728+4185G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722678 | |||||||
| chr22:45722699 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.728+4206C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722699 | |||||||
| chr22:45722822 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.728+4329A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45722822 | |||||||
| chr22:45723072 | G | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0281 a0001c0001t0001g0297 |
3 | HG02647.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.728+4579G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723072 | |||||||
| chr22:45723076 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+4583G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723076 | |||||||
| chr22:45723165 | GTA | G | 11 | a0001c0001t0001g0137 a0001c0001t0001g0281 a0001c0001t0001g0288 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.728+4684_728+4685d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45723165 | ||||||
| chr22:45723409 | G | C | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.728+4916G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723409 | |||||||
| chr22:45723436 | G | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | NA18942.hp1 NA18951.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+4943G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723436 | |||||||
| chr22:45723553 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.728+5060G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723553 | |||||||
| chr22:45723656 | C | G | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+5163C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723656 | |||||||
| chr22:45723886 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.728+5393G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723886 | |||||||
| chr22:45723951 | C | CA | 7 | a0001c0001t0001g0164 a0001c0001t0001g0176 a0001c0001t0001g0282 others(4): Show |
7 | HG00738.hp2 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.729-5460dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45723951 | ||||||
| chr22:45723951 | CA | C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.729-5460delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45723951 | ||||||
| chr22:45723966 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.729-5459T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45723966 | |||||||
| chr22:45724046 | GTA | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.729-5365_729-5364d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45724046 | ||||||
| chr22:45724082 | C | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
105 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.729-5343C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724082 | |||||||
| chr22:45724150 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.729-5275G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724150 | |||||||
| chr22:45724174 | G | GT | 4 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-5250dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45724174 | ||||||
| chr22:45724263 | T | G | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.729-5162T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724263 | |||||||
| chr22:45724282 | C | T | 6 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0084 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-5143C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724282 | |||||||
| chr22:45724287 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.729-5138A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724287 | |||||||
| chr22:45724288 | T | G | 2 | a0001c0001t0008g0299 a0001c0001t0008g0301 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.729-5137T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724288 | |||||||
| chr22:45724426 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.729-4999G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724426 | |||||||
| chr22:45724588 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.729-4837T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724588 | |||||||
| chr22:45724701 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.729-4724A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45724701 | |||||||
| chr22:45725067 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.729-4358A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725067 | |||||||
| chr22:45725244 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.729-4181G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725244 | |||||||
| chr22:45725350 | T | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.729-4075T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725350 | |||||||
| chr22:45725401 | AT | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
75 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.729-4006delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45725401 | ||||||
| chr22:45725401 | ATT | A | 18 | a0001c0001t0001g0069 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.729-4007_729-4006d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45725401 | ||||||
| chr22:45725404 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.729-4021T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725404 | |||||||
| chr22:45725453 | T | G | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-3972T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725453 | |||||||
| chr22:45725517 | T | C | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.729-3908T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725517 | |||||||
| chr22:45725539 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0002g0046 |
3 | NA18988.hp1 NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.729-3886A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725539 | |||||||
| chr22:45725574 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0149 |
2 | NA18963.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.729-3851T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725574 | |||||||
| chr22:45725715 | G | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.729-3710G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725715 | |||||||
| chr22:45725757 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.729-3668A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725757 | |||||||
| chr22:45725767 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.729-3658C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725767 | |||||||
| chr22:45725839 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.729-3586C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45725839 | |||||||
| chr22:45726161 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.729-3264C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726161 | |||||||
| chr22:45726322 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.729-3103T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726322 | |||||||
| chr22:45726454 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.729-2971A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726454 | |||||||
| chr22:45726455 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.729-2970T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726455 | |||||||
| chr22:45726456 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.729-2969T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726456 | |||||||
| chr22:45726524 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.729-2901A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726524 | |||||||
| chr22:45726668 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.729-2757T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726668 | |||||||
| chr22:45726750 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.729-2675C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726750 | |||||||
| chr22:45726873 | T | A | 1 | a0001c0001t0002g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.729-2552T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726873 | |||||||
| chr22:45727000 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.729-2425A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727000 | |||||||
| chr22:45727017 | T | TG | 13 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.729-2407dupG | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727017 | ||||||
| chr22:45727053 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.729-2372G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727053 | |||||||
| chr22:45727168 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.729-2257G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727168 | |||||||
| chr22:45727327 | ATCTATAT others(5): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.729-2096_729-2085d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727327 | ||||||
| chr22:45727331 | A | ATATC | 85 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
85 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.729-2052_729-2049d others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727331 | ||||||
| chr22:45727331 | A | ATATCTAT others(1): Show |
161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
161 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.729-2056_729-2049d others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727331 | ||||||
| chr22:45727331 | A | ATATCTAT others(5): Show |
1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.729-2084_729-2083i others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727331 | ||||||
| chr22:45727331 | A | ATATCTAT others(5): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
14 | HG00140.hp2 HG02135.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.729-2060_729-2049d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727331 | ||||||
| chr22:45727331 | A | ATATCTAT others(9): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0182 |
3 | HG03209.hp2 HG04199.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.729-2064_729-2049d others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 45727331 | ||||||
| chr22:45727581 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729-1844G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727581 | |||||||
| chr22:45727612 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0048 others(1): Show |
4 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-1813C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727612 | |||||||
| chr22:45727682 | A | G | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.729-1743A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727682 | |||||||
| chr22:45727762 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.729-1663G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727762 | |||||||
| chr22:45727835 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.729-1590A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727835 | |||||||
| chr22:45727880 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-1545A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45727880 | |||||||
| chr22:45728308 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.729-1117T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45728308 | |||||||
| chr22:45728346 | A | T | 2 | a0001c0001t0001g0265 a0001c0001t0002g0203 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.729-1079A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45728346 | |||||||
| chr22:45728386 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.729-1039G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45728386 | |||||||
| chr22:45728832 | A | G | 32 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.729-593A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45728832 | |||||||
| chr22:45729158 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.729-267A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45729158 | |||||||
| chr22:45729616 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.894+26C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45729616 | |||||||
| chr22:45729693 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(2): Show |
5 | HG01975.hp1 NA18989.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+103T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45729693 | |||||||
| chr22:45730245 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+655G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730245 | |||||||
| chr22:45730318 | C | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.894+728C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730318 | |||||||
| chr22:45730336 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.894+746C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730336 | |||||||
| chr22:45730344 | C | CA | 40 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(37): Show |
40 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.894+773dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45730344 | ||||||
| chr22:45730344 | CAAA | C | 37 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(34): Show |
37 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.894+771_894+773del others(3): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45730344 | ||||||
| chr22:45730396 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.894+806A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730396 | |||||||
| chr22:45730654 | C | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.894+1064C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730654 | |||||||
| chr22:45730688 | C | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0313 |
3 | HG02145.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.894+1098C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730688 | |||||||
| chr22:45730781 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0003g0125 |
2 | HG01106.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.894+1191C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730781 | |||||||
| chr22:45730823 | A | G | 43 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(40): Show |
43 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.894+1233A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730823 | |||||||
| chr22:45730967 | G | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0214 a0001c0001t0002g0131 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.894+1377G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730967 | |||||||
| chr22:45730998 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.894+1408T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45730998 | |||||||
| chr22:45731028 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.894+1438T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731028 | |||||||
| chr22:45731040 | G | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0084 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.894+1450G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731040 | |||||||
| chr22:45731047 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0106 |
2 | HG00140.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.894+1457G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731047 | |||||||
| chr22:45731389 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.894+1799A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731389 | |||||||
| chr22:45731475 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.894+1885A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731475 | |||||||
| chr22:45731581 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0002g0213 |
3 | HG02965.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.894+1991T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731581 | |||||||
| chr22:45731651 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.894+2061A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731651 | |||||||
| chr22:45731832 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.894+2242C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731832 | |||||||
| chr22:45731934 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.894+2344G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45731934 | |||||||
| chr22:45732290 | CA | C | 41 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(38): Show |
41 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.894+2710delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45732290 | ||||||
| chr22:45732313 | G | T | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.894+2723G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732313 | |||||||
| chr22:45732314 | C | T | 1 | a0001c0001t0015g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.894+2724C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732314 | |||||||
| chr22:45732316 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.894+2726G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732316 | |||||||
| chr22:45732375 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.894+2785C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732375 | |||||||
| chr22:45732425 | T | G | 1 | a0001c0001t0002g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.894+2835T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732425 | |||||||
| chr22:45732574 | CT | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0085 others(8): Show |
11 | HG01099.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.894+2999delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45732574 | ||||||
| chr22:45732581 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894+2991T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45732581 | |||||||
| chr22:45733053 | A | G | 21 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.894+3463A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45733053 | |||||||
| chr22:45733629 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.894+4039G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45733629 | |||||||
| chr22:45733687 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+4097C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45733687 | |||||||
| chr22:45733704 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.894+4114T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45733704 | |||||||
| chr22:45734056 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.894+4466T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734056 | |||||||
| chr22:45734318 | A | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0121 |
2 | NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.895-4413A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734318 | |||||||
| chr22:45734530 | A | AT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(49): Show |
52 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.895-4184dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734530 | ||||||
| chr22:45734574 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.895-4157G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734574 | |||||||
| chr22:45734800 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-3931T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734800 | |||||||
| chr22:45734869 | A | ATAT | 84 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.895-3833_895-3831d others(5): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTAT | 27 | a0001c0001t0001g0055 a0001c0001t0001g0073 a0001c0001t0001g0074 others(24): Show |
27 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.895-3836_895-3831d others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTATT others(2): Show |
16 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0080 others(13): Show |
16 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-3839_895-3831d others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTATT others(5): Show |
37 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(34): Show |
37 | HG00408.hp1 HG01891.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.895-3842_895-3831d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTATT others(8): Show |
33 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0068 others(30): Show |
33 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.895-3845_895-3831d others(17): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTATT others(11): Show |
1 | a0001c0001t0002g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.895-3848_895-3831d others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734869 | A | ATATTATT others(14): Show |
1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.895-3851_895-3831d others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45734869 | ||||||
| chr22:45734924 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-3807G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734924 | |||||||
| chr22:45734952 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.895-3779T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45734952 | |||||||
| chr22:45735126 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.895-3605G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735126 | |||||||
| chr22:45735151 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.895-3580T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735151 | |||||||
| chr22:45735174 | C | T | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.895-3557C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735174 | |||||||
| chr22:45735295 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.895-3436A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735295 | |||||||
| chr22:45735320 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-3411G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735320 | |||||||
| chr22:45735358 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.895-3373G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735358 | |||||||
| chr22:45735756 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.895-2975T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735756 | |||||||
| chr22:45735757 | C | CT | 37 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.895-2963dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45735757 | ||||||
| chr22:45735789 | C | T | 3 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0018g0118 |
3 | HG01884.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.895-2942C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45735789 | |||||||
| chr22:45735812 | CT | C | 92 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0115 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.895-2896delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45735812 | ||||||
| chr22:45735812 | CTT | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
103 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.895-2897_895-2896d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45735812 | ||||||
| chr22:45735812 | CTTTTT | C | 37 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(34): Show |
37 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.895-2900_895-2896d others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45735812 | ||||||
| chr22:45735812 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18970.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.895-2910_895-2896d others(17): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45735812 | ||||||
| chr22:45736148 | G | A | 25 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(22): Show |
25 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.895-2583G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736148 | |||||||
| chr22:45736165 | T | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0302 |
2 | NA18953.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.895-2566T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736165 | |||||||
| chr22:45736304 | A | G | 80 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0142 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.895-2427A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736304 | |||||||
| chr22:45736384 | A | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0313 |
3 | HG02145.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.895-2347A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736384 | |||||||
| chr22:45736421 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-2310C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736421 | |||||||
| chr22:45736460 | AAACACCT others(25): Show |
A | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0005g0291 others(1): Show |
4 | HG01891.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-2250_895-2219d others(34): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45736460 | ||||||
| chr22:45736489 | C | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-2242C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736489 | |||||||
| chr22:45736492 | TAACACCT others(10): Show |
T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-2238_895-2222d others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736492 | |||||||
| chr22:45736510 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-2221G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736510 | |||||||
| chr22:45736538 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.895-2193G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736538 | |||||||
| chr22:45736574 | T | A | 1 | a0001c0001t0001g0237 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.895-2157T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736574 | |||||||
| chr22:45736606 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02135.hp1 NA18951.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2125T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736606 | |||||||
| chr22:45736704 | A | G | 5 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(2): Show |
5 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-2027A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736704 | |||||||
| chr22:45736793 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-1938G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736793 | |||||||
| chr22:45736793 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.895-1938G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736793 | |||||||
| chr22:45736880 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0004g0140 a0001c0001t0004g0244 |
3 | HG03669.hp1 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.895-1851A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736880 | |||||||
| chr22:45736960 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-1771A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45736960 | |||||||
| chr22:45737081 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.895-1650C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737081 | |||||||
| chr22:45737129 | G | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.895-1602G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737129 | |||||||
| chr22:45737162 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.895-1569C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737162 | |||||||
| chr22:45737203 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.895-1528G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737203 | |||||||
| chr22:45737204 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.895-1527G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737204 | |||||||
| chr22:45737230 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-1501A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737230 | |||||||
| chr22:45737270 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.895-1461G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737270 | |||||||
| chr22:45737301 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.895-1430G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737301 | |||||||
| chr22:45737359 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.895-1372C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737359 | |||||||
| chr22:45737430 | T | G | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.895-1301T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737430 | |||||||
| chr22:45737447 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.895-1284A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737447 | |||||||
| chr22:45737690 | C | CT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0063 others(17): Show |
20 | HG00738.hp2 HG02135.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.895-1019dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45737690 | ||||||
| chr22:45737690 | CT | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(6): Show |
9 | HG01070.hp1 HG01109.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-1019delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45737690 | ||||||
| chr22:45737690 | CTT | C | 9 | a0001c0001t0001g0070 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.895-1020_895-1019d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 45737690 | ||||||
| chr22:45737715 | T | C | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1016T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737715 | |||||||
| chr22:45737960 | C | T | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.895-771C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737960 | |||||||
| chr22:45737973 | A | G | 51 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.895-758A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45737973 | |||||||
| chr22:45738122 | TC | T | 9 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
9 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-608delC | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738122 | |||||||
| chr22:45738148 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.895-583A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738148 | |||||||
| chr22:45738183 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.895-548C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738183 | |||||||
| chr22:45738233 | C | G | 7 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.895-498C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738233 | |||||||
| chr22:45738468 | T | G | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.895-263T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738468 | |||||||
| chr22:45738557 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.895-174G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 7/11 | chr22 | 45738557 | |||||||
| chr22:45738954 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1003+115A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45738954 | |||||||
| chr22:45739053 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1003+214G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739053 | |||||||
| chr22:45739120 | A | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003+281A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739120 | |||||||
| chr22:45739158 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1003+319G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739158 | |||||||
| chr22:45739551 | A | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1003+712A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739551 | |||||||
| chr22:45739714 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1004-655T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739714 | |||||||
| chr22:45739806 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1004-563G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45739806 | |||||||
| chr22:45740228 | G | A | 18 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(15): Show |
18 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1004-141G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 8/11 | chr22 | 45740228 | |||||||
| chr22:45740608 | C | G | 8 | a0001c0001t0001g0130 a0001c0001t0001g0214 a0001c0001t0002g0131 others(5): Show |
8 | HG02572.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+70C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740608 | |||||||
| chr22:45740612 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1173+74C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740612 | |||||||
| chr22:45740679 | T | TAC | 19 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.1173+181_1173+182d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | T | TACAC | 10 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01109.hp1 HG04199.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+179_1173+182d others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | T | TACACAC | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0111 |
3 | HG02056.hp2 NA18939.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1173+177_1173+182d others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TAC | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0217 a0001c0001t0001g0264 others(4): Show |
7 | HG00140.hp2 HG00738.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+181_1173+182d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACAC | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0078 a0001c0001t0001g0091 others(42): Show |
45 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1173+179_1173+182d others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACACAC | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0068 others(143): Show |
147 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1173+177_1173+182d others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACACACA others(1): Show |
T | 25 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0073 others(22): Show |
25 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1173+175_1173+182d others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACACACA others(3): Show |
T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0210 a0001c0001t0001g0273 |
3 | HG02622.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1173+173_1173+182d others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACACACA others(5): Show |
T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+171_1173+182d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740679 | TACACACA others(7): Show |
T | 1 | a0003c0002t0001g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1173+169_1173+182d others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740679 | ||||||
| chr22:45740709 | CACACACA others(5): Show |
C | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1173+173_1173+184d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740709 | ||||||
| chr22:45740709 | CACACACA others(49): Show |
C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1173+173_1173+228d others(58): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740709 | ||||||
| chr22:45740711 | CACACACA others(5): Show |
C | 3 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0018g0118 |
3 | HG01884.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1173+175_1173+186d others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740711 | ||||||
| chr22:45740715 | C | T | 1 | a0001c0001t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1173+177C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740715 | |||||||
| chr22:45740717 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0092 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1173+179C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740717 | |||||||
| chr22:45740719 | C | CACACACA others(9): Show |
1 | a0001c0001t0005g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1173+182_1173+183i others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740719 | ||||||
| chr22:45740719 | C | CACACACA others(5): Show |
1 | a0001c0001t0012g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1173+182_1173+183i others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740719 | ||||||
| chr22:45740719 | C | CACACATA others(3): Show |
2 | a0001c0001t0001g0288 a0001c0001t0001g0295 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+182_1173+183i others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740719 | ||||||
| chr22:45740719 | C | CACATACA others(1): Show |
4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0293 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+182_1173+183i others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740719 | ||||||
| chr22:45740719 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0070 others(89): Show |
93 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1173+181C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740719 | |||||||
| chr22:45740721 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 |
3 | NA18944.hp2 NA18953.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1173+183T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740721 | |||||||
| chr22:45740727 | T | C | 13 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG01943.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+189T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740727 | |||||||
| chr22:45740729 | C | T | 144 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(141): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1173+191C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740729 | |||||||
| chr22:45740737 | C | T | 11 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1173+199C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740737 | |||||||
| chr22:45740738 | A | G | 11 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1173+200A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740738 | |||||||
| chr22:45740739 | C | CGT | 86 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0085 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1173+216_1173+217d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740739 | ||||||
| chr22:45740739 | C | CGTGT | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+214_1173+217d others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740739 | ||||||
| chr22:45740739 | C | T | 12 | a0001c0001t0001g0281 a0001c0001t0001g0288 a0001c0001t0001g0289 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+201C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740739 | |||||||
| chr22:45740740 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1173+202G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740740 | |||||||
| chr22:45740741 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1173+203T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740741 | |||||||
| chr22:45740754 | G | GTA | 39 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1173+228_1173+229d others(4): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45740754 | ||||||
| chr22:45740756 | A | G | 12 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
12 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1173+218A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740756 | |||||||
| chr22:45740768 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1173+230G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740768 | |||||||
| chr22:45740900 | C | T | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1173+362C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45740900 | |||||||
| chr22:45741002 | G | T | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1173+464G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741002 | |||||||
| chr22:45741039 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173+501T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741039 | |||||||
| chr22:45741361 | A | G | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(36): Show |
39 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1173+823A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741361 | |||||||
| chr22:45741598 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1173+1060C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741598 | |||||||
| chr22:45741637 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+1099T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741637 | |||||||
| chr22:45741650 | A | C | 24 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(21): Show |
24 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1173+1112A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741650 | |||||||
| chr22:45741689 | G | GA | 7 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+1161dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45741689 | ||||||
| chr22:45741700 | T | A | 2 | a0001c0001t0001g0271 a0001c0001t0006g0087 |
2 | HG00642.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1173+1162T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741700 | |||||||
| chr22:45741752 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 |
3 | NA18981.hp1 NA19007.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1173+1214T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741752 | |||||||
| chr22:45741821 | C | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+1283C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45741821 | |||||||
| chr22:45742124 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01943.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1173+1586C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742124 | |||||||
| chr22:45742439 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1173+1901A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742439 | |||||||
| chr22:45742530 | TA | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1173+2005delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45742530 | ||||||
| chr22:45742594 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1173+2056A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742594 | |||||||
| chr22:45742641 | G | A | 12 | a0001c0001t0001g0137 a0001c0001t0001g0288 a0001c0001t0001g0289 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+2103G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742641 | |||||||
| chr22:45742744 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0003g0122 a0001c0001t0003g0123 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+2206G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742744 | |||||||
| chr22:45742801 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1173+2263A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742801 | |||||||
| chr22:45742833 | TC | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0062 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1173+2301delC | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45742833 | ||||||
| chr22:45742877 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+2339T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45742877 | |||||||
| chr22:45743022 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0012g0081 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+2484A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45743022 | |||||||
| chr22:45744048 | G | A | 4 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+3510G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744048 | |||||||
| chr22:45744150 | T | C | 10 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
10 | HG02129.hp1 HG02135.hp1 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+3612T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744150 | |||||||
| chr22:45744223 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1173+3685A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744223 | |||||||
| chr22:45744553 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1173+4015T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744553 | |||||||
| chr22:45744575 | G | C | 27 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0107 others(24): Show |
27 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1173+4037G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744575 | |||||||
| chr22:45744593 | G | A | 61 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(58): Show |
61 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.1173+4055G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744593 | |||||||
| chr22:45744644 | T | G | 1 | a0001c0001t0002g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1173+4106T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45744644 | |||||||
| chr22:45745146 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+4608C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745146 | |||||||
| chr22:45745275 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1173+4737A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745275 | |||||||
| chr22:45745286 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1173+4748A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745286 | |||||||
| chr22:45745332 | C | G | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1173+4794C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745332 | |||||||
| chr22:45745379 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+4841T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745379 | |||||||
| chr22:45745499 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+4961A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745499 | |||||||
| chr22:45745655 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1173+5117T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745655 | |||||||
| chr22:45745671 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1173+5133G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745671 | |||||||
| chr22:45745708 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1173+5170C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745708 | |||||||
| chr22:45745791 | A | C | 1 | a0001c0001t0001g0001 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1173+5253A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745791 | |||||||
| chr22:45745819 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+5281G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745819 | |||||||
| chr22:45745995 | A | G | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+5457A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45745995 | |||||||
| chr22:45746073 | A | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0121 |
2 | NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1173+5535A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746073 | |||||||
| chr22:45746153 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1173+5615C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746153 | |||||||
| chr22:45746214 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1173+5676A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746214 | |||||||
| chr22:45746273 | A | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1173+5735A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746273 | |||||||
| chr22:45746351 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02723.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1173+5813G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746351 | |||||||
| chr22:45746352 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0017 |
2 | NA18953.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1173+5814C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746352 | |||||||
| chr22:45746363 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+5825G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746363 | |||||||
| chr22:45746426 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0270 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1173+5888G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746426 | |||||||
| chr22:45746634 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0085 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1173+6096G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746634 | |||||||
| chr22:45746634 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1173+6096G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746634 | |||||||
| chr22:45746663 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1173+6125A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746663 | |||||||
| chr22:45746672 | C | CT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0138 others(68): Show |
72 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1173+6137dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45746672 | ||||||
| chr22:45746757 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): Show |
48 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1173+6219C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746757 | |||||||
| chr22:45746785 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
260 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.1173+6247G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746785 | |||||||
| chr22:45746928 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0080 others(26): Show |
29 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1173+6390G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746928 | |||||||
| chr22:45746954 | A | G | 22 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0072 others(19): Show |
22 | HG01099.hp2 HG01891.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.1173+6416A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746954 | |||||||
| chr22:45746986 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1173+6448A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45746986 | |||||||
| chr22:45747220 | G | T | 1 | a0001c0001t0004g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1173+6682G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747220 | |||||||
| chr22:45747223 | C | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(123): Show |
126 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1173+6685C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747223 | |||||||
| chr22:45747244 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+6706G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747244 | |||||||
| chr22:45747276 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(2): Show |
5 | HG02717.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+6738C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747276 | |||||||
| chr22:45747437 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1173+6899G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747437 | |||||||
| chr22:45747445 | A | G | 10 | a0001c0001t0001g0069 a0001c0001t0001g0130 a0001c0001t0001g0272 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+6907A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747445 | |||||||
| chr22:45747453 | G | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02723.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+6915G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747453 | |||||||
| chr22:45747464 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1173+6926A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747464 | |||||||
| chr22:45747591 | G | A | 10 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0079 others(7): Show |
10 | HG00738.hp2 HG01099.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+7053G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747591 | |||||||
| chr22:45747693 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1173+7155G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747693 | |||||||
| chr22:45747717 | A | C | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1173+7179A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747717 | |||||||
| chr22:45747938 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1173+7400C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747938 | |||||||
| chr22:45747979 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1173+7441G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45747979 | |||||||
| chr22:45748014 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1173+7476C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748014 | |||||||
| chr22:45748025 | C | T | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1173+7487C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748025 | |||||||
| chr22:45748166 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1173+7628G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748166 | |||||||
| chr22:45748179 | TA | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0160 a0001c0001t0001g0271 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1173+7655delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45748179 | ||||||
| chr22:45748180 | A | T | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1173+7642A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748180 | |||||||
| chr22:45748204 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1173+7666G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748204 | |||||||
| chr22:45748221 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0115 |
2 | HG03490.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1173+7683A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748221 | |||||||
| chr22:45748557 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+8019G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748557 | |||||||
| chr22:45748558 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | NA18963.hp1 NA18979.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+8020C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748558 | |||||||
| chr22:45748625 | A | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+8087A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748625 | |||||||
| chr22:45748627 | A | G | 27 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(24): Show |
27 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1173+8089A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748627 | |||||||
| chr22:45748640 | A | G | 5 | a0001c0001t0001g0141 a0001c0001t0001g0241 a0001c0001t0004g0140 others(2): Show |
5 | HG02109.hp1 HG03669.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+8102A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748640 | |||||||
| chr22:45748726 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1173+8188T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748726 | |||||||
| chr22:45748737 | T | G | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1173+8199T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748737 | |||||||
| chr22:45748748 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1173+8210T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748748 | |||||||
| chr22:45748875 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+8337C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748875 | |||||||
| chr22:45748972 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1173+8434C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45748972 | |||||||
| chr22:45749110 | CTAGGCTC others(15): Show |
C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1173+8574_1173+859 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45749110 | ||||||
| chr22:45749139 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0236 a0001c0001t0001g0238 |
4 | HG03239.hp2 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+8601A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749139 | |||||||
| chr22:45749169 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173+8631C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749169 | |||||||
| chr22:45749222 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1173+8684G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749222 | |||||||
| chr22:45749296 | G | T | 78 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(75): Show |
78 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1173+8758G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749296 | |||||||
| chr22:45749381 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1173+8843A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749381 | |||||||
| chr22:45749639 | T | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.1173+9101T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749639 | |||||||
| chr22:45749735 | T | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1173+9197T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749735 | |||||||
| chr22:45749805 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+9267G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749805 | |||||||
| chr22:45749822 | T | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+9284T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749822 | |||||||
| chr22:45749854 | C | T | 8 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+9316C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749854 | |||||||
| chr22:45749926 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(142): Show |
146 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1173+9388G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45749926 | |||||||
| chr22:45750206 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1173+9668C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750206 | |||||||
| chr22:45750207 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0114 |
2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1173+9669G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750207 | |||||||
| chr22:45750217 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+9679C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750217 | |||||||
| chr22:45750249 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+9711C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750249 | |||||||
| chr22:45750335 | G | T | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1173+9797G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750335 | |||||||
| chr22:45750565 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1173+10027A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750565 | |||||||
| chr22:45750628 | T | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+10090T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750628 | |||||||
| chr22:45750729 | G | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+10191G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750729 | |||||||
| chr22:45750911 | A | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0265 a0001c0001t0008g0299 others(1): Show |
4 | HG02572.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10373A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750911 | |||||||
| chr22:45750939 | G | GT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(143): Show |
147 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1173+10410dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45750939 | ||||||
| chr22:45750950 | A | C | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+10412A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45750950 | |||||||
| chr22:45750953 | C | CA | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10416dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45750953 | ||||||
| chr22:45751013 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1173+10475C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751013 | |||||||
| chr22:45751119 | C | CG | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+10585dupG | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751119 | ||||||
| chr22:45751146 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1173+10608G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751146 | |||||||
| chr22:45751182 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1173+10644C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751182 | |||||||
| chr22:45751303 | A | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+10765A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751303 | |||||||
| chr22:45751427 | T | TGA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(141): Show |
145 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1173+10911_1173+10 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751427 | ||||||
| chr22:45751427 | TGA | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0253 a0001c0001t0007g0205 others(1): Show |
4 | HG03225.hp2 NA18982.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+10911_1173+10 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751427 | ||||||
| chr22:45751615 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1173+11077C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751615 | |||||||
| chr22:45751644 | T | G | 1 | a0001c0001t0002g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1173+11106T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751644 | |||||||
| chr22:45751673 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1173+11135G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751673 | |||||||
| chr22:45751680 | T | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0001c0001t0001g0188 others(1): Show |
4 | NA18951.hp2 NA18975.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+11142T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751680 | |||||||
| chr22:45751707 | T | G | 7 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11169T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751707 | |||||||
| chr22:45751739 | GGA | G | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAA | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0080 |
3 | HG01891.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(9): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(3): Show |
G | 7 | a0001c0001t0001g0270 a0001c0001t0001g0296 a0001c0001t0003g0126 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(4): Show |
G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0210 a0001c0001t0001g0265 others(2): Show |
5 | HG02622.hp1 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(17): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(5): Show |
G | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0068 others(5): Show |
8 | HG01243.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(6): Show |
G | 79 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(76): Show |
79 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(7): Show |
G | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1173+11202_1173+11 others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751739 | GGAAAAAA others(9): Show |
G | 3 | a0001c0001t0001g0253 a0001c0001t0007g0205 a0001c0001t0007g0206 |
3 | NA18982.hp1 NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1173+11202_1173+11 others(22): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751739 | |||||||
| chr22:45751740 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0069 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1173+11202G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751740 | |||||||
| chr22:45751740 | G | GA | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
50 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1173+11216dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751740 | ||||||
| chr22:45751741 | A | G | 4 | a0001c0001t0001g0115 a0001c0001t0002g0101 a0001c0001t0004g0112 others(1): Show |
4 | HG03239.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+11203A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751741 | |||||||
| chr22:45751744 | A | AT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
7 | HG00408.hp2 HG03490.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11206_1173+11 others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751744 | |||||||
| chr22:45751745 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1173+11217_1173+11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751745 | ||||||
| chr22:45751752 | AAATAAAA others(7): Show |
A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp2 HG01981.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+11220_1173+11 others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751752 | ||||||
| chr22:45751753 | AATAAAAA others(6): Show |
A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0082 others(60): Show |
64 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1173+11217_1173+11 others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751753 | ||||||
| chr22:45751754 | ATAAAAAA others(5): Show |
A | 24 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(21): Show |
24 | HG01099.hp2 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1173+11217_1173+11 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751754 | |||||||
| chr22:45751755 | T | A | 148 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0063 others(145): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1173+11217T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751755 | |||||||
| chr22:45751755 | TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0160 others(4): Show |
7 | HG01106.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11220_1173+11 others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751755 | ||||||
| chr22:45751756 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1173+11218A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751756 | |||||||
| chr22:45751758 | AAAAAAAA others(4): Show |
A | 8 | a0001c0001t0001g0078 a0001c0001t0001g0137 a0001c0001t0001g0293 others(5): Show |
8 | HG01433.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+11223_1173+11 others(17): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751758 | ||||||
| chr22:45751759 | AAAAAAAT others(3): Show |
A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1173+11224_1173+11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751759 | ||||||
| chr22:45751760 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0091 |
2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1173+11225_1173+11 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751760 | ||||||
| chr22:45751761 | AAAAATAA others(4): Show |
A | 2 | a0001c0001t0001g0086 a0001c0001t0005g0291 |
2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1173+11226_1173+11 others(17): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751761 | ||||||
| chr22:45751763 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG01070.hp1 HG01071.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(25): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0002g0100 a0001c0001t0002g0106 |
2 | HG00140.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(24): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0002g0099 a0001c0001t0002g0155 |
2 | HG00408.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0097 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(24): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0108 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(27): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(22): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0002g0098 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(28): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(11): Show |
3 | a0001c0001t0002g0094 a0001c0001t0002g0101 a0001c0001t0002g0105 |
3 | HG03239.hp1 HG03831.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(24): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0002g0090 a0001c0001t0002g0109 |
2 | NA18961.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(27): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0002g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0002g0110 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(24): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAAATA others(14): Show |
1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1173+11227_1173+11 others(27): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAATAA others(10): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0093 |
2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AAAAATAA others(13): Show |
2 | a0001c0001t0002g0116 a0001c0001t0002g0245 |
2 | HG02602.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1173+11227_1173+11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | AATAATAA others(13): Show |
1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1173+11226_1173+11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751763 | ||||||
| chr22:45751763 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | NA19070.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1173+11225A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751763 | |||||||
| chr22:45751766 | T | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0253 others(5): Show |
8 | HG00544.hp2 HG00738.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+11228T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751766 | |||||||
| chr22:45751769 | T | A | 25 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(22): Show |
25 | HG00140.hp1 HG01099.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1173+11231T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751769 | |||||||
| chr22:45751777 | A | T | 1 | a0001c0001t0002g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1173+11239A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751777 | |||||||
| chr22:45751836 | A | G | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+11298A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751836 | |||||||
| chr22:45751843 | GT | G | 9 | a0001c0001t0001g0107 a0001c0001t0001g0130 a0001c0001t0002g0095 others(6): Show |
9 | HG01433.hp2 HG02572.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+11324delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751843 | ||||||
| chr22:45751843 | GTT | G | 77 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1173+11323_1173+11 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751843 | ||||||
| chr22:45751843 | GTTT | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(163): Show |
167 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1173+11322_1173+11 others(9): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45751843 | ||||||
| chr22:45751965 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0195 |
2 | NA18957.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1173+11427G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751965 | |||||||
| chr22:45751977 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1173+11439G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45751977 | |||||||
| chr22:45752121 | A | G | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+11583A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752121 | |||||||
| chr22:45752208 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+11670G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752208 | |||||||
| chr22:45752278 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173+11740C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752278 | |||||||
| chr22:45752384 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+11846T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752384 | |||||||
| chr22:45752407 | A | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0313 |
3 | HG02145.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1173+11869A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752407 | |||||||
| chr22:45752485 | A | T | 7 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11947A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752485 | |||||||
| chr22:45752536 | AGGGGTTG others(17): Show |
A | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+12009_1173+12 others(30): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45752536 | ||||||
| chr22:45752565 | T | C | 68 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0142 others(65): Show |
68 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1173+12027T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752565 | |||||||
| chr22:45752565 | T | TTGGGGC | 98 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0082 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.1173+12054_1173+12 others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45752565 | ||||||
| chr22:45752565 | T | TTGGGGCT others(5): Show |
5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+12048_1173+12 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45752565 | ||||||
| chr22:45752612 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0048 others(1): Show |
4 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+12074C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752612 | |||||||
| chr22:45752696 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+12158G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752696 | |||||||
| chr22:45752743 | C | CT | 8 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+12217dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45752743 | ||||||
| chr22:45752772 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0297 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+12234C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752772 | |||||||
| chr22:45752827 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+12289A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752827 | |||||||
| chr22:45752882 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1173+12344C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45752882 | |||||||
| chr22:45753219 | A | AT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0138 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1173+12691dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753219 | ||||||
| chr22:45753242 | T | C | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1173+12704T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753242 | |||||||
| chr22:45753268 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0072 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1173+12730T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753268 | |||||||
| chr22:45753315 | A | G | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1173+12777A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753315 | |||||||
| chr22:45753376 | GCTTTTTT others(15): Show |
G | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1173+12839_1173+12 others(28): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753376 | |||||||
| chr22:45753377 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1173+12876_1173+12 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1173+12869_1173+12 others(25): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0012 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1173+12860_1173+12 others(34): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTT | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
16 | HG00408.hp2 HG00423.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1173+12883_1173+12 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTT | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(9): Show |
12 | HG00558.hp2 HG00597.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1173+12882_1173+12 others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1173+12878_1173+12 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02976.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1173+12876_1173+12 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+12875_1173+12 others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0008g0299 |
3 | HG02809.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1173+12874_1173+12 others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(8): Show |
C | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0092 others(4): Show |
7 | HG02109.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+12873_1173+12 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(9): Show |
C | 13 | a0001c0001t0001g0059 a0001c0001t0001g0115 a0001c0001t0002g0046 others(10): Show |
13 | HG00140.hp2 HG03239.hp1 NA18961.hp1 others(10): Show |
intron_variant | MODIFIER | c.1173+12872_1173+12 others(22): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(10): Show |
C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0068 others(17): Show |
20 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1173+12871_1173+12 others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(11): Show |
C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0162 a0001c0001t0001g0194 others(2): Show |
5 | HG00423.hp1 HG01884.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+12870_1173+12 others(24): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(12): Show |
C | 44 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0148 others(41): Show |
44 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1173+12869_1173+12 others(25): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(13): Show |
C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(100): Show |
104 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1173+12868_1173+12 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(14): Show |
C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0265 |
3 | HG02622.hp1 NA19070.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1173+12867_1173+12 others(27): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(15): Show |
C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0063 others(17): Show |
20 | HG00642.hp1 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1173+12866_1173+12 others(28): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(16): Show |
C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0085 others(7): Show |
10 | HG00099.hp2 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+12865_1173+12 others(29): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(17): Show |
C | 13 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0079 others(10): Show |
13 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1173+12864_1173+12 others(30): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(18): Show |
C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0130 others(6): Show |
9 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+12863_1173+12 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753377 | CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1173+12859_1173+12 others(35): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45753377 | ||||||
| chr22:45753399 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1173+12861T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753399 | |||||||
| chr22:45753445 | G | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1173+12907G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753445 | |||||||
| chr22:45753501 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+12963G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753501 | |||||||
| chr22:45753523 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1173+12985C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753523 | |||||||
| chr22:45753575 | C | T | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1173+13037C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753575 | |||||||
| chr22:45753598 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1173+13060G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753598 | |||||||
| chr22:45753699 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0224 |
2 | NA19003.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1173+13161G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753699 | |||||||
| chr22:45753866 | G | T | 9 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(6): Show |
9 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+13328G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753866 | |||||||
| chr22:45753959 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1173+13421T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753959 | |||||||
| chr22:45753991 | C | G | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1173+13453C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753991 | |||||||
| chr22:45753996 | C | T | 31 | a0001c0001t0001g0053 a0001c0001t0001g0092 a0001c0001t0001g0115 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1173+13458C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45753996 | |||||||
| chr22:45754091 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0114 |
2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1173+13553G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754091 | |||||||
| chr22:45754113 | AT | A | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+13576delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754113 | |||||||
| chr22:45754168 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(182): Show |
186 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1173+13630G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754168 | |||||||
| chr22:45754624 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1173+14086C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754624 | |||||||
| chr22:45754769 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1173+14231C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754769 | |||||||
| chr22:45754770 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1173+14232G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754770 | |||||||
| chr22:45754844 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1173+14306G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754844 | |||||||
| chr22:45754901 | C | T | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+14363C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45754901 | |||||||
| chr22:45755058 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1173+14520G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755058 | |||||||
| chr22:45755132 | C | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01099.hp2 HG02615.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+14594C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755132 | |||||||
| chr22:45755241 | C | T | 37 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0130 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1173+14703C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755241 | |||||||
| chr22:45755259 | A | G | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+14721A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755259 | |||||||
| chr22:45755442 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0179 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1173+14904G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755442 | |||||||
| chr22:45755538 | T | C | 37 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0144 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1173+15000T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755538 | |||||||
| chr22:45755556 | G | T | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+15018G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45755556 | |||||||
| chr22:45756000 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0072 others(174): Show |
178 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1173+15462C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756000 | |||||||
| chr22:45756075 | C | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1173+15537C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756075 | |||||||
| chr22:45756135 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173+15597T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756135 | |||||||
| chr22:45756147 | C | CT | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+15622dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45756147 | ||||||
| chr22:45756157 | T | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1173+15619T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756157 | |||||||
| chr22:45756167 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+15629A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756167 | |||||||
| chr22:45756168 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+15630C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756168 | |||||||
| chr22:45756243 | C | T | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+15705C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756243 | |||||||
| chr22:45756263 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+15725A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756263 | |||||||
| chr22:45756867 | C | T | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1173+16329C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756867 | |||||||
| chr22:45756925 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1173+16387G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756925 | |||||||
| chr22:45757071 | A | G | 9 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
9 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+16533A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757071 | |||||||
| chr22:45757100 | C | T | 28 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1173+16562C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757100 | |||||||
| chr22:45757266 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+16728G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757266 | |||||||
| chr22:45757609 | GA | G | 30 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+17082delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45757609 | ||||||
| chr22:45757645 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0254 a0001c0001t0001g0255 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+17107G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757645 | |||||||
| chr22:45757702 | G | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+17164G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757702 | |||||||
| chr22:45757759 | T | C | 4 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+17221T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757759 | |||||||
| chr22:45757823 | A | G | 3 | a0001c0001t0002g0213 a0001c0001t0005g0071 a0001c0001t0014g0077 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1173+17285A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757823 | |||||||
| chr22:45757885 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1173+17347G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45757885 | |||||||
| chr22:45758018 | G | A | 43 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1173+17480G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758018 | |||||||
| chr22:45758193 | C | T | 14 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0083 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1173+17655C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758193 | |||||||
| chr22:45758401 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+17863A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758401 | |||||||
| chr22:45758416 | G | A | 1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+17878G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758416 | |||||||
| chr22:45758486 | G | A | 68 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1173+17948G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758486 | |||||||
| chr22:45758523 | G | A | 4 | a0001c0001t0002g0095 a0001c0001t0002g0100 a0001c0001t0002g0106 others(1): Show |
4 | HG00140.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+17985G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758523 | |||||||
| chr22:45758717 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1173+18179G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758717 | |||||||
| chr22:45758844 | A | G | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(15): Show |
18 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1173+18306A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45758844 | |||||||
| chr22:45759053 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(146): Show |
150 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1173+18515C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759053 | |||||||
| chr22:45759149 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+18611G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759149 | |||||||
| chr22:45759150 | A | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+18612A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759150 | |||||||
| chr22:45759369 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+18831G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759369 | |||||||
| chr22:45759576 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+19038C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759576 | |||||||
| chr22:45759668 | C | G | 68 | a0001c0001t0001g0115 a0001c0001t0001g0142 a0001c0001t0001g0144 others(65): Show |
68 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1173+19130C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759668 | |||||||
| chr22:45759823 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+19285A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759823 | |||||||
| chr22:45759929 | A | G | 14 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(11): Show |
14 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1173+19391A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45759929 | |||||||
| chr22:45760193 | T | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+19655T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760193 | |||||||
| chr22:45760354 | C | T | 8 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+19816C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760354 | |||||||
| chr22:45760390 | T | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+19852T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760390 | |||||||
| chr22:45760408 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+19870G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760408 | |||||||
| chr22:45760532 | C | G | 7 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0161 others(4): Show |
7 | HG00597.hp2 HG00621.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+19994C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760532 | |||||||
| chr22:45760566 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+20028G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760566 | |||||||
| chr22:45760692 | A | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+20154A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760692 | |||||||
| chr22:45760701 | C | T | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+20163C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760701 | |||||||
| chr22:45760725 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1173+20187T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760725 | |||||||
| chr22:45760742 | C | A | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+20204C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760742 | |||||||
| chr22:45760810 | T | A | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+20272T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760810 | |||||||
| chr22:45760945 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0138 others(69): Show |
73 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1173+20407G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760945 | |||||||
| chr22:45760972 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1173+20434A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45760972 | |||||||
| chr22:45761077 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1173+20539A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761077 | |||||||
| chr22:45761128 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1173+20590T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761128 | |||||||
| chr22:45761161 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1173+20623G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761161 | |||||||
| chr22:45761167 | T | G | 13 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+20629T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761167 | |||||||
| chr22:45761170 | G | A | 1 | a0001c0001t0013g0019 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1173+20632G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761170 | |||||||
| chr22:45761237 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1173+20699C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761237 | |||||||
| chr22:45761314 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1173+20776C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761314 | |||||||
| chr22:45761401 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1173+20863T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761401 | |||||||
| chr22:45761506 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1173+20968T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761506 | |||||||
| chr22:45761783 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1173+21245C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761783 | |||||||
| chr22:45761948 | T | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1173+21410T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45761948 | |||||||
| chr22:45762037 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1173+21499A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762037 | |||||||
| chr22:45762098 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1173+21560C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762098 | |||||||
| chr22:45762138 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1173+21600G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762138 | |||||||
| chr22:45762255 | T | C | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1173+21717T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762255 | |||||||
| chr22:45762276 | C | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+21738C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762276 | |||||||
| chr22:45762759 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0008g0299 a0001c0001t0008g0301 |
3 | HG03098.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1173+22221A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45762759 | |||||||
| chr22:45763156 | C | G | 3 | a0001c0001t0001g0265 a0001c0001t0008g0299 a0001c0001t0008g0301 |
3 | HG03098.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1173+22618C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45763156 | |||||||
| chr22:45763511 | C | T | 9 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0187 others(6): Show |
9 | HG02129.hp1 HG02135.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+22973C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45763511 | |||||||
| chr22:45763734 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+23196G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45763734 | |||||||
| chr22:45763837 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0073 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1173+23299G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45763837 | |||||||
| chr22:45763841 | A | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+23303A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45763841 | |||||||
| chr22:45764086 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1173+23548C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764086 | |||||||
| chr22:45764134 | C | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1173+23596C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764134 | |||||||
| chr22:45764228 | A | AC | 32 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0023 others(29): Show |
32 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1173+23696dupC | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45764228 | ||||||
| chr22:45764382 | G | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+23844G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764382 | |||||||
| chr22:45764402 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1173+23864C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764402 | |||||||
| chr22:45764545 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1173+24007G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764545 | |||||||
| chr22:45764691 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+24153C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764691 | |||||||
| chr22:45764744 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(219): Show |
223 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1173+24206G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45764744 | |||||||
| chr22:45765111 | G | A | 65 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(62): Show |
65 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1173+24573G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765111 | |||||||
| chr22:45765151 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1173+24613A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765151 | |||||||
| chr22:45765167 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0265 |
2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1173+24629G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765167 | |||||||
| chr22:45765302 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+24764A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765302 | |||||||
| chr22:45765349 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+24811C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765349 | |||||||
| chr22:45765541 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1173+25003C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765541 | |||||||
| chr22:45765719 | C | T | 2 | a0001c0001t0008g0299 a0001c0001t0008g0301 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1173+25181C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765719 | |||||||
| chr22:45765884 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+25346A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765884 | |||||||
| chr22:45765995 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0072 others(175): Show |
179 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1173+25457A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45765995 | |||||||
| chr22:45766196 | A | G | 8 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+25658A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766196 | |||||||
| chr22:45766430 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+25892C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766430 | |||||||
| chr22:45766596 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+26058A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766596 | |||||||
| chr22:45766628 | A | G | 15 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0079 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1173+26090A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766628 | |||||||
| chr22:45766638 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+26100C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766638 | |||||||
| chr22:45766679 | T | TTTTATC | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+26141_1173+26 others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766679 | |||||||
| chr22:45766680 | A | C | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+26142A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766680 | |||||||
| chr22:45766681 | C | A | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+26143C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766681 | |||||||
| chr22:45766683 | T | A | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+26145T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766683 | |||||||
| chr22:45766820 | A | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+26282A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45766820 | |||||||
| chr22:45767118 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(146): Show |
150 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1173+26580G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767118 | |||||||
| chr22:45767120 | A | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1173+26582A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767120 | |||||||
| chr22:45767373 | G | A | 31 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0002g0046 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1173+26835G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767373 | |||||||
| chr22:45767436 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01099.hp2 HG02615.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+26898T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767436 | |||||||
| chr22:45767436 | T | TAC | 19 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0124 others(16): Show |
19 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1173+26915_1173+26 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45767436 | ||||||
| chr22:45767442 | C | T | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1173+26904C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767442 | |||||||
| chr22:45767453 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0012g0081 |
3 | HG02572.hp2 HG03490.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+26915A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767453 | |||||||
| chr22:45767483 | A | G | 2 | a0001c0001t0008g0299 a0001c0001t0008g0301 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1173+26945A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767483 | |||||||
| chr22:45767522 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02280.hp2 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+26984A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767522 | |||||||
| chr22:45767524 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1173+26986G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767524 | |||||||
| chr22:45767556 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1173+27018T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767556 | |||||||
| chr22:45767571 | A | G | 1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+27033A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767571 | |||||||
| chr22:45767782 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1173+27244C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767782 | |||||||
| chr22:45767870 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+27332C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45767870 | |||||||
| chr22:45768202 | T | G | 1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+27664T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768202 | |||||||
| chr22:45768227 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1173+27689A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768227 | |||||||
| chr22:45768244 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1173+27706G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768244 | |||||||
| chr22:45768284 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1173+27746G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768284 | |||||||
| chr22:45768287 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1173+27749G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768287 | |||||||
| chr22:45768327 | A | G | 4 | a0001c0001t0002g0203 a0001c0001t0002g0213 a0001c0001t0005g0071 others(1): Show |
4 | HG00738.hp2 HG02280.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+27789A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768327 | |||||||
| chr22:45768398 | G | A | 15 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0079 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1173+27860G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768398 | |||||||
| chr22:45768444 | A | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0297 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+27906A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768444 | |||||||
| chr22:45768510 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1173+27972A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768510 | |||||||
| chr22:45768616 | C | A | 1 | a0001c0001t0001g0007 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1173+28078C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45768616 | |||||||
| chr22:45769221 | C | A | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+28683C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769221 | |||||||
| chr22:45769227 | A | C | 1 | a0001c0001t0009g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1173+28689A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769227 | |||||||
| chr22:45769281 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0012g0081 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+28743T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769281 | |||||||
| chr22:45769492 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173+28954G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769492 | |||||||
| chr22:45769513 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1173+28975T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769513 | |||||||
| chr22:45769553 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0012g0081 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+29015A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769553 | |||||||
| chr22:45769579 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0004g0140 a0001c0001t0004g0225 others(1): Show |
4 | HG03669.hp1 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+29041A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769579 | |||||||
| chr22:45769723 | G | C | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+29185G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769723 | |||||||
| chr22:45769726 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1173+29188T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769726 | |||||||
| chr22:45769866 | T | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+29328T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45769866 | |||||||
| chr22:45770094 | C | CA | 20 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0073 others(17): Show |
20 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1173+29558dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45770094 | ||||||
| chr22:45770223 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+29685A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770223 | |||||||
| chr22:45770266 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1173+29728G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770266 | |||||||
| chr22:45770371 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1173+29833G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770371 | |||||||
| chr22:45770578 | TG | T | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+30042delG | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45770578 | ||||||
| chr22:45770718 | A | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+30180A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770718 | |||||||
| chr22:45770773 | G | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1173+30235G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770773 | |||||||
| chr22:45770941 | C | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0121 |
3 | NA18961.hp1 NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1173+30403C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45770941 | |||||||
| chr22:45771028 | C | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 |
3 | HG01891.hp1 HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+30490C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771028 | |||||||
| chr22:45771237 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1173+30699A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771237 | |||||||
| chr22:45771260 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1173+30722C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771260 | |||||||
| chr22:45771331 | A | AT | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+30797dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45771331 | ||||||
| chr22:45771379 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1173+30841G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771379 | |||||||
| chr22:45771389 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0202 |
2 | NA19060.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1173+30851A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771389 | |||||||
| chr22:45771413 | C | CT | 34 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(31): Show |
34 | HG00597.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1173+30893dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45771413 | ||||||
| chr22:45771441 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1173+30903G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771441 | |||||||
| chr22:45771627 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0279 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+31089G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771627 | |||||||
| chr22:45771669 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+31131G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771669 | |||||||
| chr22:45771671 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1173+31133G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771671 | |||||||
| chr22:45771690 | T | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+31152T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771690 | |||||||
| chr22:45771712 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1173+31174C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771712 | |||||||
| chr22:45771823 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1173+31285G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771823 | |||||||
| chr22:45771844 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+31306A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45771844 | |||||||
| chr22:45772015 | A | G | 26 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(23): Show |
26 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1173+31477A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772015 | |||||||
| chr22:45772114 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1173+31576C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772114 | |||||||
| chr22:45772174 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1173+31636A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772174 | |||||||
| chr22:45772193 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+31655T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772193 | |||||||
| chr22:45772249 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0298 |
2 | NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1173+31711A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772249 | |||||||
| chr22:45772383 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1173+31845C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772383 | |||||||
| chr22:45772620 | C | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0250 others(1): Show |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+32082C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772620 | |||||||
| chr22:45772643 | G | C | 1 | a0001c0001t0002g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1173+32105G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772643 | |||||||
| chr22:45772764 | G | A | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+32226G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772764 | |||||||
| chr22:45772892 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1173+32354T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772892 | |||||||
| chr22:45772974 | A | G | 1 | a0001c0001t0005g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1173+32436A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45772974 | |||||||
| chr22:45773254 | C | G | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+32716C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773254 | |||||||
| chr22:45773330 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1173+32792C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773330 | |||||||
| chr22:45773445 | A | ATTAT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(90): Show |
94 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1173+32934_1173+32 others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773445 | ||||||
| chr22:45773445 | A | ATTATTTA others(1): Show |
5 | a0001c0001t0001g0195 a0001c0001t0001g0238 a0001c0001t0001g0306 others(2): Show |
5 | HG00140.hp2 HG03239.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+32930_1173+32 others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773445 | ||||||
| chr22:45773445 | A | ATTATTTA others(9): Show |
1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1173+32922_1173+32 others(22): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773445 | ||||||
| chr22:45773445 | A | ATTATTTA others(21): Show |
1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1173+32910_1173+32 others(34): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773445 | ||||||
| chr22:45773484 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1173+32946T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773484 | |||||||
| chr22:45773666 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1173+33128C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773666 | |||||||
| chr22:45773844 | A | ATGTT | 32 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1174-33097_1174-33 others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773844 | ||||||
| chr22:45773844 | ATGTT | A | 4 | a0001c0001t0006g0087 a0001c0001t0006g0119 a0001c0001t0006g0120 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-33097_1174-33 others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45773844 | ||||||
| chr22:45773857 | T | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG01433.hp1 HG02109.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-33102T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773857 | |||||||
| chr22:45773917 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1174-33042T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773917 | |||||||
| chr22:45773985 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0155 |
2 | HG02071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1174-32974G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45773985 | |||||||
| chr22:45774117 | T | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-32842T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774117 | |||||||
| chr22:45774230 | G | C | 1 | a0001c0001t0004g0225 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1174-32729G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774230 | |||||||
| chr22:45774396 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-32563C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774396 | |||||||
| chr22:45774708 | G | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-32251G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774708 | |||||||
| chr22:45774818 | A | C | 10 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-32141A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774818 | |||||||
| chr22:45774887 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1174-32072C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774887 | |||||||
| chr22:45774893 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1174-32066T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774893 | |||||||
| chr22:45774906 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0188 |
2 | NA18951.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1174-32053C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774906 | |||||||
| chr22:45774993 | T | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(1): Show |
4 | NA18963.hp1 NA18980.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-31966T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45774993 | |||||||
| chr22:45775039 | G | A | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1174-31920G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775039 | |||||||
| chr22:45775160 | C | G | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1174-31799C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775160 | |||||||
| chr22:45775299 | TGGACCTC others(6): Show |
T | 1 | a0001c0001t0001g0003 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1174-31657_1174-31 others(19): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45775299 | ||||||
| chr22:45775416 | C | T | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02280.hp2 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-31543C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775416 | |||||||
| chr22:45775625 | G | A | 30 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1174-31334G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775625 | |||||||
| chr22:45775667 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-31292G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775667 | |||||||
| chr22:45775711 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1174-31248C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775711 | |||||||
| chr22:45775850 | TC | T | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-31108delC | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775850 | |||||||
| chr22:45775852 | A | T | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-31107A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775852 | |||||||
| chr22:45775964 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0265 |
2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1174-30995C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775964 | |||||||
| chr22:45775975 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1174-30984G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775975 | |||||||
| chr22:45775982 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1174-30977A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45775982 | |||||||
| chr22:45776123 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-30836A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776123 | |||||||
| chr22:45776159 | A | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0250 others(1): Show |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-30800A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776159 | |||||||
| chr22:45776235 | T | C | 10 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG02109.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-30724T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776235 | |||||||
| chr22:45776408 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1174-30551C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776408 | |||||||
| chr22:45776449 | A | T | 1 | a0001c0001t0003g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1174-30510A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776449 | |||||||
| chr22:45776456 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1174-30503A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776456 | |||||||
| chr22:45776492 | C | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1174-30467C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776492 | |||||||
| chr22:45776496 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1174-30463C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776496 | |||||||
| chr22:45776518 | T | TA | 16 | a0001c0001t0001g0277 a0001c0001t0002g0131 a0001c0001t0002g0132 others(13): Show |
16 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-30439dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45776518 | ||||||
| chr22:45776548 | C | G | 16 | a0001c0001t0001g0277 a0001c0001t0002g0131 a0001c0001t0002g0132 others(13): Show |
16 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-30411C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776548 | |||||||
| chr22:45776687 | GA | G | 16 | a0001c0001t0001g0277 a0001c0001t0002g0131 a0001c0001t0002g0132 others(13): Show |
16 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-30268delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45776687 | ||||||
| chr22:45776713 | A | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-30246A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776713 | |||||||
| chr22:45776746 | G | A | 30 | a0001c0001t0001g0092 a0001c0001t0001g0297 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1174-30213G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776746 | |||||||
| chr22:45776806 | T | C | 20 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(17): Show |
20 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1174-30153T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776806 | |||||||
| chr22:45776975 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(231): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1174-29984G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776975 | |||||||
| chr22:45777098 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1174-29861T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777098 | |||||||
| chr22:45777207 | GC | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-29750delC | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45777207 | ||||||
| chr22:45777400 | G | C | 1 | a0001c0001t0005g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1174-29559G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777400 | |||||||
| chr22:45777704 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-29255G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777704 | |||||||
| chr22:45777746 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1174-29213G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777746 | |||||||
| chr22:45777894 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-29065C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777894 | |||||||
| chr22:45777938 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1174-29021T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45777938 | |||||||
| chr22:45778177 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1174-28782C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778177 | |||||||
| chr22:45778354 | C | T | 5 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(2): Show |
5 | HG00099.hp2 HG00735.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-28605C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778354 | |||||||
| chr22:45778562 | C | T | 9 | a0001c0001t0001g0216 a0001c0001t0001g0256 a0001c0001t0001g0257 others(6): Show |
9 | HG00673.hp1 HG02145.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-28397C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778562 | |||||||
| chr22:45778677 | T | G | 3 | a0001c0001t0002g0213 a0001c0001t0005g0071 a0001c0001t0014g0077 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-28282T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778677 | |||||||
| chr22:45778738 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1174-28221A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778738 | |||||||
| chr22:45778990 | G | A | 14 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0083 others(11): Show |
14 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1174-27969G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45778990 | |||||||
| chr22:45779127 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-27832C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779127 | |||||||
| chr22:45779128 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-27831G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779128 | |||||||
| chr22:45779331 | G | A | 9 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0172 others(6): Show |
9 | HG00423.hp1 HG00673.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-27628G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779331 | |||||||
| chr22:45779341 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-27618A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779341 | |||||||
| chr22:45779650 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0138 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1174-27309A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779650 | |||||||
| chr22:45779695 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-27264A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779695 | |||||||
| chr22:45779837 | G | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-27122G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45779837 | |||||||
| chr22:45780034 | G | A | 33 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(30): Show |
33 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1174-26925G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780034 | |||||||
| chr22:45780086 | CT | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0062 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1174-26858delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45780086 | ||||||
| chr22:45780241 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1174-26718G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780241 | |||||||
| chr22:45780393 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-26566C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780393 | |||||||
| chr22:45780482 | G | GCAGACCT others(15): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1174-26456_1174-26 others(28): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45780482 | ||||||
| chr22:45780528 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-26431C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780528 | |||||||
| chr22:45780581 | C | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0238 others(28): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1174-26378C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780581 | |||||||
| chr22:45780681 | A | C | 5 | a0001c0001t0006g0087 a0001c0001t0006g0119 a0001c0001t0006g0120 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-26278A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780681 | |||||||
| chr22:45780795 | C | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-26164C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780795 | |||||||
| chr22:45780889 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1174-26070G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780889 | |||||||
| chr22:45780942 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1174-26017C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45780942 | |||||||
| chr22:45781129 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1174-25830A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781129 | |||||||
| chr22:45781167 | T | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG00738.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-25792T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781167 | |||||||
| chr22:45781227 | C | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1174-25732C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781227 | |||||||
| chr22:45781336 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1174-25623C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781336 | |||||||
| chr22:45781434 | A | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-25525A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781434 | |||||||
| chr22:45781566 | T | A | 38 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.1174-25393T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781566 | |||||||
| chr22:45781587 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1174-25372G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781587 | |||||||
| chr22:45781875 | GA | G | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1174-25077delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45781875 | ||||||
| chr22:45781965 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0061 |
3 | HG00642.hp1 HG01255.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1174-24994T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45781965 | |||||||
| chr22:45782129 | T | C | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1174-24830T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782129 | |||||||
| chr22:45782213 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-24746T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782213 | |||||||
| chr22:45782303 | T | C | 51 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.1174-24656T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782303 | |||||||
| chr22:45782331 | G | A | 5 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(2): Show |
5 | HG00099.hp2 HG00735.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-24628G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782331 | |||||||
| chr22:45782369 | G | A | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1174-24590G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782369 | |||||||
| chr22:45782373 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0208 |
2 | HG02602.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1174-24586G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782373 | |||||||
| chr22:45782499 | G | A | 66 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(63): Show |
66 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1174-24460G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782499 | |||||||
| chr22:45782605 | C | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-24354C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782605 | |||||||
| chr22:45782729 | G | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02723.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-24230G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45782729 | |||||||
| chr22:45782967 | TACA | T | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1174-23984_1174-23 others(9): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45782967 | ||||||
| chr22:45783533 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1174-23426C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783533 | |||||||
| chr22:45783657 | C | T | 66 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0142 others(63): Show |
66 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1174-23302C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783657 | |||||||
| chr22:45783783 | T | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-23176T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783783 | |||||||
| chr22:45783844 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-23115T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783844 | |||||||
| chr22:45783940 | T | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-23019T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783940 | |||||||
| chr22:45783962 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-22997G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783962 | |||||||
| chr22:45783982 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1174-22977C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45783982 | |||||||
| chr22:45784006 | C | A | 1 | a0001c0001t0001g0007 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1174-22953C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784006 | |||||||
| chr22:45784098 | C | A | 3 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0018g0118 |
3 | HG01884.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1174-22861C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784098 | |||||||
| chr22:45784103 | C | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-22856C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784103 | |||||||
| chr22:45784181 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(186): Show |
190 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1174-22778A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784181 | |||||||
| chr22:45784182 | A | T | 3 | a0001c0001t0001g0141 a0001c0001t0004g0244 a0001c0001t0007g0206 |
3 | HG03704.hp1 HG03704.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1174-22777A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784182 | |||||||
| chr22:45784240 | A | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG01433.hp1 HG02109.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-22719A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784240 | |||||||
| chr22:45784415 | C | G | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1174-22544C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784415 | |||||||
| chr22:45784440 | T | C | 41 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(38): Show |
41 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1174-22519T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784440 | |||||||
| chr22:45784444 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1174-22515A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784444 | |||||||
| chr22:45784469 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-22490C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784469 | |||||||
| chr22:45784591 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1174-22368G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784591 | |||||||
| chr22:45784627 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1174-22332G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784627 | |||||||
| chr22:45784707 | A | G | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-22252A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784707 | |||||||
| chr22:45784835 | G | A | 8 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(5): Show |
8 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-22124G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784835 | |||||||
| chr22:45784883 | T | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-22076T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784883 | |||||||
| chr22:45784892 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1174-22067T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784892 | |||||||
| chr22:45784984 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1174-21975T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784984 | |||||||
| chr22:45785212 | T | TG | 4 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-21745dupG | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45785212 | ||||||
| chr22:45785216 | G | A | 14 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0083 others(11): Show |
14 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1174-21743G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45785216 | |||||||
| chr22:45785440 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-21519T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45785440 | |||||||
| chr22:45785586 | A | C | 1 | a0001c0001t0002g0093 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1174-21373A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45785586 | |||||||
| chr22:45785974 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-20985A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45785974 | |||||||
| chr22:45786333 | A | G | 8 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(5): Show |
8 | HG02280.hp2 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-20626A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786333 | |||||||
| chr22:45786501 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1174-20458C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786501 | |||||||
| chr22:45786542 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0313 |
2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1174-20417C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786542 | |||||||
| chr22:45786809 | G | A | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-20150G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786809 | |||||||
| chr22:45786876 | G | A | 67 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(64): Show |
67 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1174-20083G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786876 | |||||||
| chr22:45786912 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(208): Show |
212 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1174-20047C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786912 | |||||||
| chr22:45786978 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-19981G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786978 | |||||||
| chr22:45787390 | G | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0184 a0001c0001t0001g0298 |
3 | HG02015.hp2 NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1174-19569G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787390 | |||||||
| chr22:45787420 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-19539G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787420 | |||||||
| chr22:45787486 | C | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-19473C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787486 | |||||||
| chr22:45787494 | T | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-19465T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787494 | |||||||
| chr22:45787576 | G | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-19383G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787576 | |||||||
| chr22:45787636 | T | C | 20 | a0001c0001t0001g0069 a0001c0001t0002g0131 a0001c0001t0002g0132 others(17): Show |
20 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1174-19323T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787636 | |||||||
| chr22:45787687 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1174-19272T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787687 | |||||||
| chr22:45787706 | G | C | 1 | a0001c0001t0002g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1174-19253G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787706 | |||||||
| chr22:45787734 | A | T | 27 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(24): Show |
27 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1174-19225A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45787734 | |||||||
| chr22:45788146 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1174-18813T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788146 | |||||||
| chr22:45788209 | A | T | 7 | a0001c0001t0002g0046 a0001c0001t0002g0090 a0001c0001t0002g0098 others(4): Show |
7 | NA18949.hp1 NA18964.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-18750A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788209 | |||||||
| chr22:45788220 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0012g0081 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-18739A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788220 | |||||||
| chr22:45788524 | G | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-18435G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788524 | |||||||
| chr22:45788547 | G | C | 46 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(43): Show |
46 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1174-18412G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788547 | |||||||
| chr22:45788560 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1174-18399G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788560 | |||||||
| chr22:45788576 | A | G | 11 | a0001c0001t0001g0069 a0001c0001t0002g0131 a0001c0001t0002g0132 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-18383A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788576 | |||||||
| chr22:45788592 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-18367T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788592 | |||||||
| chr22:45788600 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1174-18359G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788600 | |||||||
| chr22:45788726 | A | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-18233A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788726 | |||||||
| chr22:45788776 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-18183T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788776 | |||||||
| chr22:45788802 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-18157A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788802 | |||||||
| chr22:45788845 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0149 |
2 | NA18963.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1174-18114C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788845 | |||||||
| chr22:45788849 | G | A | 8 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(5): Show |
8 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-18110G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788849 | |||||||
| chr22:45788885 | A | G | 47 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1174-18074A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788885 | |||||||
| chr22:45788917 | A | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-18042A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788917 | |||||||
| chr22:45788979 | G | A | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(15): Show |
18 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1174-17980G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45788979 | |||||||
| chr22:45789058 | A | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-17901A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789058 | |||||||
| chr22:45789113 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1174-17846A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789113 | |||||||
| chr22:45789244 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-17715G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789244 | |||||||
| chr22:45789272 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(9): Show |
12 | NA18963.hp1 NA18970.hp2 NA18979.hp1 others(9): Show |
intron_variant | MODIFIER | c.1174-17687G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789272 | |||||||
| chr22:45789302 | G | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1174-17657G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789302 | |||||||
| chr22:45789313 | T | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-17646T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789313 | |||||||
| chr22:45789362 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1174-17597G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789362 | |||||||
| chr22:45789400 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG00140.hp1 HG00738.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1174-17559C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789400 | |||||||
| chr22:45789407 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1174-17552G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789407 | |||||||
| chr22:45789569 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0082 others(142): Show |
146 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1174-17390G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789569 | |||||||
| chr22:45789673 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0315 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1174-17286G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789673 | |||||||
| chr22:45789741 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(1): Show |
4 | NA18963.hp1 NA18980.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-17218T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789741 | |||||||
| chr22:45789993 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1174-16966G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45789993 | |||||||
| chr22:45790012 | T | G | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1174-16947T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790012 | |||||||
| chr22:45790103 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-16856A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790103 | |||||||
| chr22:45790107 | C | T | 24 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(21): Show |
24 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1174-16852C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790107 | |||||||
| chr22:45790572 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1174-16387G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790572 | |||||||
| chr22:45790585 | A | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-16374A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790585 | |||||||
| chr22:45790738 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0012g0081 |
3 | HG02647.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-16221A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790738 | |||||||
| chr22:45790799 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-16160A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790799 | |||||||
| chr22:45790883 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1174-16076C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790883 | |||||||
| chr22:45790894 | G | A | 1 | a0001c0001t0018g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1174-16065G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45790894 | |||||||
| chr22:45791045 | G | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-15914G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791045 | |||||||
| chr22:45791103 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1174-15856C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791103 | |||||||
| chr22:45791237 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0056 |
3 | HG02135.hp2 NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1174-15722A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791237 | |||||||
| chr22:45791269 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1174-15690T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791269 | |||||||
| chr22:45791337 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-15622A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791337 | |||||||
| chr22:45791345 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1174-15614A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791345 | |||||||
| chr22:45791353 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-15606G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791353 | |||||||
| chr22:45791422 | C | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-15537C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791422 | |||||||
| chr22:45791433 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1174-15526G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791433 | |||||||
| chr22:45791647 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-15312A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791647 | |||||||
| chr22:45791756 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1174-15203G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791756 | |||||||
| chr22:45791789 | C | T | 1 | a0001c0001t0006g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1174-15170C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45791789 | |||||||
| chr22:45791951 | A | AAAATTTT others(66): Show |
1 | a0001c0001t0001g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1174-14992_1174-14 others(79): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45791951 | ||||||
| chr22:45792003 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1174-14956A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792003 | |||||||
| chr22:45792038 | C | A | 1 | a0001c0001t0002g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1174-14921C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792038 | |||||||
| chr22:45792162 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1174-14797A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792162 | |||||||
| chr22:45792203 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1174-14756G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792203 | |||||||
| chr22:45792211 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0250 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1174-14748G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792211 | |||||||
| chr22:45792258 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1174-14701A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792258 | |||||||
| chr22:45792917 | G | A | 41 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(38): Show |
41 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.1174-14042G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792917 | |||||||
| chr22:45792926 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-14033A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792926 | |||||||
| chr22:45792935 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0056 |
2 | NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1174-14024A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45792935 | |||||||
| chr22:45793265 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1174-13694G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793265 | |||||||
| chr22:45793310 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1174-13649G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793310 | |||||||
| chr22:45793352 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1174-13607G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793352 | |||||||
| chr22:45793363 | T | TA | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-13596_1174-13 others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793363 | |||||||
| chr22:45793370 | T | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-13589T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793370 | |||||||
| chr22:45793552 | A | AT | 12 | a0001c0001t0002g0203 a0001c0001t0002g0213 a0001c0001t0003g0122 others(9): Show |
12 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-13406dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45793552 | ||||||
| chr22:45793552 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0217 a0001c0001t0001g0306 |
3 | NA18957.hp2 NA19070.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1174-13407A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45793552 | |||||||
| chr22:45794080 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0046 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1174-12879G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794080 | |||||||
| chr22:45794084 | A | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-12875A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794084 | |||||||
| chr22:45794118 | A | G | 3 | a0001c0001t0002g0213 a0001c0001t0005g0071 a0001c0001t0014g0077 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-12841A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794118 | |||||||
| chr22:45794157 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0082 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1174-12802A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794157 | |||||||
| chr22:45794193 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1174-12766T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794193 | |||||||
| chr22:45794228 | C | G | 3 | a0001c0001t0002g0213 a0001c0001t0005g0071 a0001c0001t0014g0077 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-12731C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794228 | |||||||
| chr22:45794301 | AT | A | 13 | a0001c0001t0001g0069 a0001c0001t0003g0122 a0001c0001t0003g0123 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1174-12651delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45794301 | ||||||
| chr22:45794303 | T | C | 13 | a0001c0001t0001g0069 a0001c0001t0003g0122 a0001c0001t0003g0123 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1174-12656T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794303 | |||||||
| chr22:45794323 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1174-12636A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794323 | |||||||
| chr22:45794384 | CAT | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-12572_1174-12 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45794384 | ||||||
| chr22:45794416 | A | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0051 others(1): Show |
4 | NA18956.hp2 NA18969.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-12543A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794416 | |||||||
| chr22:45794448 | T | TA | 13 | a0001c0001t0001g0141 a0001c0001t0001g0167 a0001c0001t0001g0175 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1174-12498dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45794448 | ||||||
| chr22:45794646 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1174-12313A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794646 | |||||||
| chr22:45794748 | C | A | 23 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
23 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1174-12211C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794748 | |||||||
| chr22:45794933 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0297 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1174-12026G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45794933 | |||||||
| chr22:45795260 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1174-11699T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795260 | |||||||
| chr22:45795346 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11613C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795346 | |||||||
| chr22:45795348 | A | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11611A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795348 | |||||||
| chr22:45795349 | G | GTAGATAG others(11218): Show |
1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11610_1174-11 others(11231): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795349 | |||||||
| chr22:45795351 | A | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11608A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795351 | |||||||
| chr22:45795353 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11606G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795353 | |||||||
| chr22:45795354 | G | GATTCT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0035 others(33): Show |
36 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1174-11539_1174-11 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | G | GATTCTAT others(3): Show |
27 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0088 others(24): Show |
27 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174-11544_1174-11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | G | GATTCTAT others(8): Show |
8 | a0001c0001t0001g0089 a0001c0001t0001g0143 a0001c0001t0001g0145 others(5): Show |
8 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-11549_1174-11 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | G | GATTCTAT others(13): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0306 a0001c0001t0002g0108 |
3 | NA18957.hp2 NA18989.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1174-11554_1174-11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | G | GATTCTAT others(18): Show |
1 | a0001c0001t0002g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1174-11559_1174-11 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1174-11605G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795354 | |||||||
| chr22:45795354 | GATTCT | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1174-11539_1174-11 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | GATTCTAT others(3): Show |
G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
46 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174-11544_1174-11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | GATTCTAT others(8): Show |
G | 7 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0124 others(4): Show |
7 | HG01099.hp2 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174-11549_1174-11 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | GATTCTAT others(13): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1174-11554_1174-11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | GATTCTAT others(18): Show |
G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | NA18985.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1174-11559_1174-11 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795354 | GATTCTAT others(28): Show |
G | 3 | a0001c0001t0001g0265 a0001c0001t0008g0299 a0001c0001t0008g0301 |
3 | HG03098.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1174-11569_1174-11 others(41): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795354 | ||||||
| chr22:45795413 | C | G | 1 | a0001c0001t0002g0097 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1174-11546C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795413 | |||||||
| chr22:45795415 | A | ATTCTATT others(28): Show |
1 | a0001c0001t0002g0110 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1174-11535_1174-11 others(41): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(23): Show |
3 | a0001c0001t0002g0046 a0001c0001t0002g0093 a0001c0001t0002g0106 |
3 | HG00140.hp2 NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1174-11535_1174-11 others(36): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(18): Show |
3 | a0001c0001t0001g0092 a0001c0001t0002g0090 a0001c0001t0002g0114 |
3 | NA18964.hp1 NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1174-11535_1174-11 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(13): Show |
3 | a0001c0001t0002g0094 a0001c0001t0002g0105 a0001c0001t0002g0116 |
3 | HG03831.hp2 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1174-11535_1174-11 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(8): Show |
5 | a0001c0001t0002g0095 a0001c0001t0002g0098 a0001c0001t0002g0100 others(2): Show |
5 | HG01168.hp2 HG01433.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-11535_1174-11 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(3): Show |
8 | a0001c0001t0002g0099 a0001c0001t0002g0108 a0001c0001t0002g0109 others(5): Show |
8 | HG00408.hp1 HG02602.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-11541_1174-11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTCTATT others(3): Show |
2 | a0001c0001t0002g0155 a0001c0001t0010g0104 |
2 | NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1174-11537_1174-11 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | ATTGTT | 3 | a0001c0001t0002g0096 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | HG01070.hp1 HG01071.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1174-11542_1174-11 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45795415 | ||||||
| chr22:45795415 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1174-11544A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795415 | |||||||
| chr22:45795423 | C | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
7 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-11536C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795423 | |||||||
| chr22:45795424 | T | TATTCTAT others(7): Show |
1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1174-11535_1174-11 others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795424 | |||||||
| chr22:45795426 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1174-11533T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795426 | |||||||
| chr22:45795428 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1174-11531T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795428 | |||||||
| chr22:45795472 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-11487G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795472 | |||||||
| chr22:45795473 | C | T | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-11486C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795473 | |||||||
| chr22:45795728 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-11231G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795728 | |||||||
| chr22:45795795 | C | T | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-11164C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795795 | |||||||
| chr22:45795911 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1174-11048T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795911 | |||||||
| chr22:45795932 | T | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-11027T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795932 | |||||||
| chr22:45795941 | T | A | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1174-11018T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45795941 | |||||||
| chr22:45796058 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1174-10901T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796058 | |||||||
| chr22:45796144 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1174-10815G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796144 | |||||||
| chr22:45796183 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-10776A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796183 | |||||||
| chr22:45796216 | T | G | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-10743T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796216 | |||||||
| chr22:45796285 | A | T | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-10674A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796285 | |||||||
| chr22:45796354 | C | A | 1 | a0001c0001t0002g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1174-10605C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796354 | |||||||
| chr22:45796356 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1174-10603T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796356 | |||||||
| chr22:45796359 | T | G | 1 | a0001c0001t0002g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1174-10600T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796359 | |||||||
| chr22:45796375 | C | T | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1174-10584C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796375 | |||||||
| chr22:45796515 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1174-10444T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796515 | |||||||
| chr22:45796515 | T | G | 1 | a0001c0001t0001g0013 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1174-10444T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796515 | |||||||
| chr22:45796533 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-10426G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796533 | |||||||
| chr22:45796679 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0298 |
2 | NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1174-10280C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796679 | |||||||
| chr22:45796698 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-10261G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796698 | |||||||
| chr22:45796720 | A | T | 14 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1174-10239A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796720 | |||||||
| chr22:45796762 | G | A | 9 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0288 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-10197G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796762 | |||||||
| chr22:45796857 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-10102A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45796857 | |||||||
| chr22:45797000 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9959A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797000 | |||||||
| chr22:45797062 | C | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-9897C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797062 | |||||||
| chr22:45797139 | C | T | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-9820C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797139 | |||||||
| chr22:45797140 | G | A | 1 | a0001c0001t0003g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1174-9819G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797140 | |||||||
| chr22:45797226 | G | A | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-9733G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797226 | |||||||
| chr22:45797297 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1174-9662A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797297 | |||||||
| chr22:45797339 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(1): Show |
4 | NA18963.hp1 NA18980.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-9620T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797339 | |||||||
| chr22:45797536 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1174-9423T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797536 | |||||||
| chr22:45797718 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9241A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797718 | |||||||
| chr22:45797779 | G | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-9180G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797779 | |||||||
| chr22:45797781 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9178T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797781 | |||||||
| chr22:45797806 | G | T | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9153G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797806 | |||||||
| chr22:45797875 | A | G | 11 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0186 others(8): Show |
11 | HG02129.hp1 HG02135.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1174-9084A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45797875 | |||||||
| chr22:45798460 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0142 |
2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1174-8499C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45798460 | |||||||
| chr22:45798574 | T | A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-8385T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45798574 | |||||||
| chr22:45798708 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1174-8251G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45798708 | |||||||
| chr22:45798789 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-8170A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45798789 | |||||||
| chr22:45798846 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-8113A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45798846 | |||||||
| chr22:45799087 | G | GT | 131 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(128): Show |
131 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.1174-7867dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45799087 | ||||||
| chr22:45799087 | G | GTT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0082 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1174-7868_1174-786 others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45799087 | ||||||
| chr22:45799087 | G | GTTT | 5 | a0001c0001t0001g0156 a0001c0001t0001g0257 a0001c0001t0001g0259 others(2): Show |
5 | HG00738.hp1 HG03130.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-7869_1174-786 others(7): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45799087 | ||||||
| chr22:45799087 | G | T | 1 | a0001c0001t0008g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1174-7872G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799087 | |||||||
| chr22:45799093 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1174-7866C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799093 | |||||||
| chr22:45799196 | G | C | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1174-7763G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799196 | |||||||
| chr22:45799215 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-7744C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799215 | |||||||
| chr22:45799377 | C | A | 2 | a0001c0001t0001g0265 a0001c0001t0008g0301 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1174-7582C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799377 | |||||||
| chr22:45799404 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-7555A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799404 | |||||||
| chr22:45799463 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-7496T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799463 | |||||||
| chr22:45799540 | A | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(5): Show |
8 | HG02280.hp2 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174-7419A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799540 | |||||||
| chr22:45799696 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174-7263C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799696 | |||||||
| chr22:45799700 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1174-7259C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799700 | |||||||
| chr22:45799704 | T | C | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0121 |
3 | NA18961.hp1 NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1174-7255T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799704 | |||||||
| chr22:45799747 | A | G | 1 | a0001c0001t0007g0205 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1174-7212A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799747 | |||||||
| chr22:45799819 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1174-7140A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799819 | |||||||
| chr22:45799834 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-7125A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45799834 | |||||||
| chr22:45800240 | T | TA | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6718dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45800240 | ||||||
| chr22:45800309 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1174-6650T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800309 | |||||||
| chr22:45800384 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1174-6575T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800384 | |||||||
| chr22:45800522 | GA | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1174-6432delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45800522 | ||||||
| chr22:45800566 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-6393A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800566 | |||||||
| chr22:45800658 | C | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0078 others(8): Show |
11 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-6301C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800658 | |||||||
| chr22:45800752 | A | G | 24 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(21): Show |
24 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1174-6207A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800752 | |||||||
| chr22:45800894 | C | T | 1 | a0001c0001t0015g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1174-6065C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800894 | |||||||
| chr22:45800988 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18970.hp2 NA19066.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-5971C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45800988 | |||||||
| chr22:45801001 | C | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1174-5958C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801001 | |||||||
| chr22:45801219 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0179 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1174-5740C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801219 | |||||||
| chr22:45801481 | A | G | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1174-5478A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801481 | |||||||
| chr22:45801600 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-5359A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801600 | |||||||
| chr22:45801669 | A | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-5290A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801669 | |||||||
| chr22:45801725 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1174-5234G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801725 | |||||||
| chr22:45801735 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1174-5224G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45801735 | |||||||
| chr22:45802200 | A | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-4759A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802200 | |||||||
| chr22:45802273 | C | T | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1174-4686C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802273 | |||||||
| chr22:45802309 | A | C | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1174-4650A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802309 | |||||||
| chr22:45802310 | A | G | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-4649A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802310 | |||||||
| chr22:45802399 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-4560A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802399 | |||||||
| chr22:45802434 | G | T | 71 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0115 others(68): Show |
71 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1174-4525G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802434 | |||||||
| chr22:45802450 | T | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0273 |
2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1174-4509T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802450 | |||||||
| chr22:45802487 | T | A | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-4472T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802487 | |||||||
| chr22:45802583 | G | A | 1 | a0001c0001t0008g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1174-4376G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802583 | |||||||
| chr22:45802599 | T | C | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-4360T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802599 | |||||||
| chr22:45802617 | C | A | 1 | a0001c0001t0002g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1174-4342C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802617 | |||||||
| chr22:45802756 | A | G | 43 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(40): Show |
43 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1174-4203A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45802756 | |||||||
| chr22:45803069 | T | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0258 |
2 | NA18942.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1174-3890T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803069 | |||||||
| chr22:45803117 | ACACT | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-3838_1174-383 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 45803117 | ||||||
| chr22:45803406 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1174-3553C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803406 | |||||||
| chr22:45803452 | G | T | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-3507G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803452 | |||||||
| chr22:45803469 | C | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0149 |
2 | NA18963.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1174-3490C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803469 | |||||||
| chr22:45803749 | C | T | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1174-3210C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803749 | |||||||
| chr22:45803771 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1174-3188C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803771 | |||||||
| chr22:45803857 | A | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-3102A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803857 | |||||||
| chr22:45803976 | C | T | 13 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1174-2983C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45803976 | |||||||
| chr22:45804131 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1174-2828G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804131 | |||||||
| chr22:45804247 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1174-2712C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804247 | |||||||
| chr22:45804261 | C | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-2698C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804261 | |||||||
| chr22:45804305 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1174-2654A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804305 | |||||||
| chr22:45804441 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0313 |
3 | HG02145.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1174-2518T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804441 | |||||||
| chr22:45804548 | G | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0219 a0001c0001t0001g0221 others(5): Show |
8 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2411G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804548 | |||||||
| chr22:45804705 | A | G | 1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-2254A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804705 | |||||||
| chr22:45804787 | C | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-2172C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804787 | |||||||
| chr22:45804957 | C | G | 72 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0115 others(69): Show |
72 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1174-2002C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804957 | |||||||
| chr22:45804979 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-1980C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45804979 | |||||||
| chr22:45805156 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1174-1803G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805156 | |||||||
| chr22:45805494 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1465G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805494 | |||||||
| chr22:45805560 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1174-1399G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805560 | |||||||
| chr22:45805603 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1174-1356C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805603 | |||||||
| chr22:45805623 | G | A | 13 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1174-1336G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805623 | |||||||
| chr22:45805671 | A | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1174-1288A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805671 | |||||||
| chr22:45805757 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1174-1202G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805757 | |||||||
| chr22:45805899 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1174-1060A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45805899 | |||||||
| chr22:45806008 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1174-951A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806008 | |||||||
| chr22:45806183 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-776A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806183 | |||||||
| chr22:45806203 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1174-756G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806203 | |||||||
| chr22:45806284 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1174-675C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806284 | |||||||
| chr22:45806295 | T | G | 14 | a0001c0001t0001g0069 a0001c0001t0002g0131 a0001c0001t0002g0132 others(11): Show |
14 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1174-664T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806295 | |||||||
| chr22:45806359 | T | C | 1 | a0001c0001t0017g0247 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1174-600T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806359 | |||||||
| chr22:45806537 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-422C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806537 | |||||||
| chr22:45806609 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-350C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806609 | |||||||
| chr22:45806610 | A | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-349A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806610 | |||||||
| chr22:45806612 | G | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-347G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806612 | |||||||
| chr22:45806895 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1174-64A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806895 | |||||||
| chr22:45806939 | C | T | 6 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(3): Show |
6 | HG01106.hp2 HG01884.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-20C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45806939 | |||||||
| chr22:45807045 | A | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1237+23A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807045 | |||||||
| chr22:45807154 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1237+132A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807154 | |||||||
| chr22:45807323 | C | T | 7 | a0001c0001t0002g0046 a0001c0001t0002g0090 a0001c0001t0002g0098 others(4): Show |
7 | NA18949.hp1 NA18964.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+301C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807323 | |||||||
| chr22:45807476 | C | T | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+454C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807476 | |||||||
| chr22:45807669 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1237+647A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807669 | |||||||
| chr22:45807718 | A | G | 1 | a0001c0001t0007g0206 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1237+696A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807718 | |||||||
| chr22:45807844 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1237+822G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807844 | |||||||
| chr22:45807974 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | HG01433.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1237+952T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45807974 | |||||||
| chr22:45808091 | G | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+1069G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808091 | |||||||
| chr22:45808209 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1237+1187C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808209 | |||||||
| chr22:45808260 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1237+1238G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808260 | |||||||
| chr22:45808262 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1237+1240A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808262 | |||||||
| chr22:45808310 | C | T | 34 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0046 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1237+1288C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808310 | |||||||
| chr22:45808545 | A | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+1523A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808545 | |||||||
| chr22:45808609 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1237+1587G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808609 | |||||||
| chr22:45808662 | C | A | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1237+1640C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808662 | |||||||
| chr22:45808906 | C | T | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(15): Show |
18 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1237+1884C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808906 | |||||||
| chr22:45808908 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1237+1886C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45808908 | |||||||
| chr22:45809098 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0179 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1237+2076C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809098 | |||||||
| chr22:45809106 | C | T | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+2084C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809106 | |||||||
| chr22:45809131 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1237+2109T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809131 | |||||||
| chr22:45809142 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237+2120T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809142 | |||||||
| chr22:45809224 | A | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG01433.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237+2202A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809224 | |||||||
| chr22:45809309 | C | T | 34 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0046 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1237+2287C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809309 | |||||||
| chr22:45809314 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1237+2292C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809314 | |||||||
| chr22:45809351 | A | G | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+2329A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809351 | |||||||
| chr22:45809434 | C | T | 11 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1237+2412C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809434 | |||||||
| chr22:45809919 | A | G | 12 | a0001c0001t0001g0069 a0001c0001t0002g0131 a0001c0001t0002g0132 others(9): Show |
12 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1237+2897A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45809919 | |||||||
| chr22:45810015 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1237+2993A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810015 | |||||||
| chr22:45810040 | CTTTATAG others(10): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1237+3020_1237+303 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45810040 | ||||||
| chr22:45810118 | A | G | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1237+3096A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810118 | |||||||
| chr22:45810136 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1237+3114T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810136 | |||||||
| chr22:45810180 | T | C | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1237+3158T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810180 | |||||||
| chr22:45810194 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1237+3172C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810194 | |||||||
| chr22:45810252 | C | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0268 |
2 | HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1237+3230C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810252 | |||||||
| chr22:45810368 | G | C | 2 | a0001c0001t0002g0213 a0001c0001t0005g0071 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1237+3346G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810368 | |||||||
| chr22:45810421 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1237+3399G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810421 | |||||||
| chr22:45810450 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1237+3428G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810450 | |||||||
| chr22:45810491 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1237+3469G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810491 | |||||||
| chr22:45810499 | C | T | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1237+3477C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810499 | |||||||
| chr22:45810541 | A | C | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+3519A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810541 | |||||||
| chr22:45810634 | C | T | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1237+3612C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810634 | |||||||
| chr22:45810635 | G | A | 35 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0046 others(32): Show |
35 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1237+3613G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810635 | |||||||
| chr22:45810736 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0012g0081 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1237+3714A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810736 | |||||||
| chr22:45810750 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+3728A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810750 | |||||||
| chr22:45810820 | C | T | 68 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1237+3798C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810820 | |||||||
| chr22:45810854 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+3832T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810854 | |||||||
| chr22:45810925 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1237+3903C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45810925 | |||||||
| chr22:45810932 | T | TA | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+3911dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45810932 | ||||||
| chr22:45811072 | T | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1237+4050T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45811072 | |||||||
| chr22:45811681 | A | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+4659A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45811681 | |||||||
| chr22:45811821 | T | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1237+4799T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45811821 | |||||||
| chr22:45811870 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1237+4848C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45811870 | |||||||
| chr22:45812075 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0062 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1237+5053T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812075 | |||||||
| chr22:45812081 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1237+5059A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812081 | |||||||
| chr22:45812099 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1237+5077C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812099 | |||||||
| chr22:45812165 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1237+5143A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812165 | |||||||
| chr22:45812537 | G | A | 28 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1237+5515G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812537 | |||||||
| chr22:45812946 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1237+5924G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45812946 | |||||||
| chr22:45813222 | A | AT | 9 | a0001c0001t0001g0160 a0001c0001t0001g0216 a0001c0001t0001g0217 others(6): Show |
9 | HG00673.hp1 HG02129.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237+6206dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45813222 | ||||||
| chr22:45813311 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+6289C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813311 | |||||||
| chr22:45813333 | G | GT | 14 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(11): Show |
14 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1237+6323dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45813333 | ||||||
| chr22:45813333 | G | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0131 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+6311G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813333 | |||||||
| chr22:45813361 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0088 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1237+6339G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813361 | |||||||
| chr22:45813361 | G | C | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1237+6339G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813361 | |||||||
| chr22:45813424 | G | GT | 8 | a0001c0001t0001g0278 a0001c0001t0002g0131 a0001c0001t0002g0132 others(5): Show |
8 | HG00738.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237+6409dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45813424 | ||||||
| chr22:45813455 | C | CT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0058 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1237+6446dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45813455 | ||||||
| chr22:45813455 | C | CTT | 30 | a0001c0001t0001g0068 a0001c0001t0001g0092 a0001c0001t0001g0115 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+6445_1237+644 others(6): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45813455 | ||||||
| chr22:45813657 | G | A | 16 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(13): Show |
16 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1237+6635G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813657 | |||||||
| chr22:45813788 | G | A | 2 | a0001c0001t0003g0125 a0001c0001t0003g0307 |
2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1237+6766G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813788 | |||||||
| chr22:45813976 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1237+6954A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45813976 | |||||||
| chr22:45814464 | T | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0265 others(7): Show |
10 | HG02572.hp2 HG02717.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237+7442T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814464 | |||||||
| chr22:45814480 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1237+7458G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814480 | |||||||
| chr22:45814683 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0253 |
2 | NA18957.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1237+7661C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814683 | |||||||
| chr22:45814723 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0315 |
3 | HG01099.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1237+7701A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814723 | |||||||
| chr22:45814800 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1237+7778C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814800 | |||||||
| chr22:45814835 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1237+7813G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814835 | |||||||
| chr22:45814959 | T | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02723.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+7937T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45814959 | |||||||
| chr22:45815334 | G | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0175 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1237+8312G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815334 | |||||||
| chr22:45815491 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1237+8469T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815491 | |||||||
| chr22:45815541 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+8519C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815541 | |||||||
| chr22:45815661 | T | C | 32 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1237+8639T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815661 | |||||||
| chr22:45815723 | T | G | 1 | a0001c0001t0004g0244 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1237+8701T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815723 | |||||||
| chr22:45815777 | G | T | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1237+8755G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815777 | |||||||
| chr22:45815797 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0253 |
2 | NA18957.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1237+8775G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815797 | |||||||
| chr22:45815857 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1237+8835T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815857 | |||||||
| chr22:45815937 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1237+8915C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815937 | |||||||
| chr22:45815976 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1237+8954G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45815976 | |||||||
| chr22:45816055 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1237+9033G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816055 | |||||||
| chr22:45816176 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1237+9154C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816176 | |||||||
| chr22:45816247 | C | CT | 31 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1237+9226dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45816247 | ||||||
| chr22:45816290 | A | G | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1237+9268A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816290 | |||||||
| chr22:45816510 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1237+9488A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816510 | |||||||
| chr22:45816737 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0277 a0001c0001t0003g0122 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1237+9715G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816737 | |||||||
| chr22:45816910 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1237+9888G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45816910 | |||||||
| chr22:45817043 | G | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1237+10021G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817043 | |||||||
| chr22:45817135 | A | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0265 a0001c0001t0008g0299 others(2): Show |
5 | HG02572.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237+10113A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817135 | |||||||
| chr22:45817184 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+10162T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817184 | |||||||
| chr22:45817318 | C | CT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG00642.hp1 HG01255.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237+10320dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45817318 | ||||||
| chr22:45817318 | CT | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1237+10320delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45817318 | ||||||
| chr22:45817318 | CTT | C | 49 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0174 others(46): Show |
49 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1237+10319_1237+10 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45817318 | ||||||
| chr22:45817318 | CTTT | C | 6 | a0001c0001t0002g0109 a0001c0001t0002g0131 a0001c0001t0002g0132 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237+10318_1237+10 others(9): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45817318 | ||||||
| chr22:45817417 | T | C | 45 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1237+10395T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817417 | |||||||
| chr22:45817429 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1237+10407A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817429 | |||||||
| chr22:45817460 | A | G | 45 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1237+10438A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817460 | |||||||
| chr22:45817496 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1237+10474T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817496 | |||||||
| chr22:45817628 | A | AT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | NA18970.hp2 NA18991.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+10619dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45817628 | ||||||
| chr22:45817641 | T | G | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237+10619T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817641 | |||||||
| chr22:45817711 | A | G | 9 | a0001c0001t0001g0069 a0001c0001t0001g0270 a0001c0001t0001g0296 others(6): Show |
9 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237+10689A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817711 | |||||||
| chr22:45817961 | T | C | 45 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0115 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1237+10939T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45817961 | |||||||
| chr22:45818106 | A | G | 7 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237+11084A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818106 | |||||||
| chr22:45818304 | G | C | 29 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0046 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1237+11282G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818304 | |||||||
| chr22:45818471 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1237+11449G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818471 | |||||||
| chr22:45818589 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1237+11567G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818589 | |||||||
| chr22:45818603 | G | A | 13 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1237+11581G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818603 | |||||||
| chr22:45818626 | G | GCAGGGAT | 14 | a0001c0001t0001g0069 a0001c0001t0001g0270 a0001c0001t0001g0296 others(11): Show |
14 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1237+11617_1237+11 others(13): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45818626 | ||||||
| chr22:45818651 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1237+11629G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818651 | |||||||
| chr22:45818824 | T | C | 72 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(69): Show |
72 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1237+11802T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818824 | |||||||
| chr22:45818840 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0296 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1237+11818T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818840 | |||||||
| chr22:45818858 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1237+11836C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818858 | |||||||
| chr22:45818874 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1237+11852A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818874 | |||||||
| chr22:45818877 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0061 |
2 | HG01255.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1237+11855C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45818877 | |||||||
| chr22:45819192 | A | AAATAG | 36 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
36 | HG00408.hp1 HG00642.hp1 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.1237+12226_1237+12 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | A | AAATAGAA others(3): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(18): Show |
21 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1237+12221_1237+12 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | A | AAATAGAA others(8): Show |
11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+12216_1237+12 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | A | AAATAGAA others(13): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1237+12211_1237+12 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | A | AAATAGAA others(18): Show |
1 | a0001c0001t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1237+12206_1237+12 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAG | A | 34 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(31): Show |
34 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1237+12226_1237+12 others(11): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(3): Show |
A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0148 others(17): Show |
20 | HG00423.hp1 HG00673.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.1237+12221_1237+12 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(8): Show |
A | 61 | a0001c0001t0001g0072 a0001c0001t0001g0088 a0001c0001t0001g0089 others(58): Show |
61 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1237+12216_1237+12 others(21): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(13): Show |
A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(67): Show |
71 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1237+12211_1237+12 others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(18): Show |
A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0270 a0001c0001t0001g0296 |
3 | HG02300.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1237+12206_1237+12 others(31): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(23): Show |
A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+12201_1237+12 others(36): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819192 | AAATAGAA others(28): Show |
A | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+12196_1237+12 others(41): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45819192 | ||||||
| chr22:45819434 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0296 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1237+12412A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45819434 | |||||||
| chr22:45819833 | T | C | 30 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+12811T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45819833 | |||||||
| chr22:45820008 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0273 |
2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1237+12986C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820008 | |||||||
| chr22:45820283 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1237+13261A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820283 | |||||||
| chr22:45820697 | G | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1237+13675G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820697 | |||||||
| chr22:45820788 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1237+13766G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820788 | |||||||
| chr22:45820884 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0149 |
2 | NA18963.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1237+13862G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820884 | |||||||
| chr22:45820956 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1237+13934T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45820956 | |||||||
| chr22:45821224 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+14202A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821224 | |||||||
| chr22:45821241 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1237+14219G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821241 | |||||||
| chr22:45821254 | C | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+14232C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821254 | |||||||
| chr22:45821258 | T | C | 2 | a0001c0001t0001g0297 a0001c0001t0012g0081 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1237+14236T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821258 | |||||||
| chr22:45821292 | G | T | 32 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0216 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1237+14270G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821292 | |||||||
| chr22:45821344 | C | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+14322C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821344 | |||||||
| chr22:45821347 | T | TA | 45 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0048 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1237+14345dupA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45821347 | ||||||
| chr22:45821347 | TA | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0197 others(4): Show |
7 | HG00738.hp2 HG01168.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+14345delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45821347 | ||||||
| chr22:45821462 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1237+14440A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821462 | |||||||
| chr22:45821608 | T | C | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0289 others(1): Show |
4 | HG02055.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+14586T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821608 | |||||||
| chr22:45821629 | G | A | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+14607G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821629 | |||||||
| chr22:45821670 | T | C | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237+14648T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821670 | |||||||
| chr22:45821714 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237+14692T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821714 | |||||||
| chr22:45821746 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0006g0087 a0001c0001t0006g0119 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237+14724T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45821746 | |||||||
| chr22:45822013 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG00738.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237+14991A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822013 | |||||||
| chr22:45822056 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0265 a0001c0001t0008g0299 others(1): Show |
4 | HG02572.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237+15034G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822056 | |||||||
| chr22:45822072 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1237+15050T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822072 | |||||||
| chr22:45822268 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+15246T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822268 | |||||||
| chr22:45822399 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1237+15377C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822399 | |||||||
| chr22:45822521 | C | T | 34 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0046 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1237+15499C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822521 | |||||||
| chr22:45822523 | A | AT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0030 others(43): Show |
46 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.1237+15526dupT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45822523 | ||||||
| chr22:45822523 | AT | A | 30 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0069 others(27): Show |
30 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1237+15526delT | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45822523 | ||||||
| chr22:45822523 | ATT | A | 30 | a0001c0001t0001g0092 a0001c0001t0001g0268 a0001c0001t0001g0269 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+15525_1237+15 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45822523 | ||||||
| chr22:45822561 | T | C | 150 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(147): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1237+15539T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822561 | |||||||
| chr22:45822565 | C | T | 28 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1237+15543C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822565 | |||||||
| chr22:45822593 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG00673.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1237+15571C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822593 | |||||||
| chr22:45822597 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1237+15575C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822597 | |||||||
| chr22:45822737 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1237+15715G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822737 | |||||||
| chr22:45822788 | T | C | 86 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(83): Show |
86 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1237+15766T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45822788 | |||||||
| chr22:45823110 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1237+16088A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823110 | |||||||
| chr22:45823148 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+16126C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823148 | |||||||
| chr22:45823330 | G | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1237+16308G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823330 | |||||||
| chr22:45823441 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0002g0203 a0001c0001t0006g0087 others(3): Show |
6 | HG00738.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237+16419T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823441 | |||||||
| chr22:45823446 | C | T | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237+16424C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823446 | |||||||
| chr22:45823465 | T | G | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237+16443T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823465 | |||||||
| chr22:45823489 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1237+16467C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823489 | |||||||
| chr22:45823541 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1237+16519G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823541 | |||||||
| chr22:45823690 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1237+16668G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823690 | |||||||
| chr22:45823772 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1237+16750A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823772 | |||||||
| chr22:45823788 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+16766C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823788 | |||||||
| chr22:45823843 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+16821A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823843 | |||||||
| chr22:45823862 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+16840C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823862 | |||||||
| chr22:45823878 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1237+16856G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823878 | |||||||
| chr22:45823931 | G | A | 23 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
23 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237+16909G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45823931 | |||||||
| chr22:45824005 | C | T | 1 | a0001c0001t0006g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1237+16983C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824005 | |||||||
| chr22:45824198 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1237+17176G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824198 | |||||||
| chr22:45824268 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1237+17246C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824268 | |||||||
| chr22:45824408 | T | C | 10 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0001c0001t0001g0187 others(7): Show |
10 | HG02135.hp1 NA18951.hp2 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237+17386T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824408 | |||||||
| chr22:45824492 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+17470C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824492 | |||||||
| chr22:45824763 | C | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0297 a0001c0001t0011g0136 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+17741C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824763 | |||||||
| chr22:45824865 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1237+17843A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45824865 | |||||||
| chr22:45825107 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0265 a0001c0001t0008g0299 others(1): Show |
4 | HG02572.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-17884G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825107 | |||||||
| chr22:45825154 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-17837C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825154 | |||||||
| chr22:45825411 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1238-17580C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825411 | |||||||
| chr22:45825434 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1238-17557C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825434 | |||||||
| chr22:45825478 | A | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0265 a0001c0001t0008g0299 others(1): Show |
4 | HG02572.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-17513A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825478 | |||||||
| chr22:45825502 | G | T | 14 | a0001c0001t0001g0069 a0001c0001t0003g0122 a0001c0001t0003g0123 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1238-17489G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825502 | |||||||
| chr22:45825578 | T | G | 2 | a0001c0001t0008g0299 a0001c0001t0008g0301 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1238-17413T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825578 | |||||||
| chr22:45825710 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-17281C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825710 | |||||||
| chr22:45825739 | G | A | 33 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(30): Show |
33 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1238-17252G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825739 | |||||||
| chr22:45825832 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1238-17159C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825832 | |||||||
| chr22:45825899 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1238-17092T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825899 | |||||||
| chr22:45825955 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(6): Show |
9 | NA18954.hp2 NA18978.hp2 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1238-17036G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45825955 | |||||||
| chr22:45826059 | C | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-16932C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45826059 | |||||||
| chr22:45826210 | G | A | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(15): Show |
18 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1238-16781G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45826210 | |||||||
| chr22:45826485 | A | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-16506A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45826485 | |||||||
| chr22:45826944 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-16047G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45826944 | |||||||
| chr22:45827036 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0277 |
2 | HG01943.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1238-15955A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827036 | |||||||
| chr22:45827129 | C | CCA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0111 |
3 | HG02056.hp2 NA18967.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1238-15820_1238-15 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCA | C | 16 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
16 | HG00597.hp1 HG01943.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1238-15820_1238-15 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACA | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0282 a0001c0001t0001g0284 |
3 | HG02976.hp1 HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1238-15822_1238-15 others(10): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACA | C | 7 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0160 others(4): Show |
7 | HG00741.hp2 HG02129.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1238-15824_1238-15 others(12): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACAC others(1): Show |
C | 17 | a0001c0001t0001g0164 a0001c0001t0001g0182 a0001c0001t0001g0208 others(14): Show |
17 | HG00673.hp1 HG01069.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1238-15826_1238-15 others(14): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACAC others(3): Show |
C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0072 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1238-15828_1238-15 others(16): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACAC others(5): Show |
C | 23 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(20): Show |
23 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1238-15830_1238-15 others(18): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACAC others(7): Show |
C | 38 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(35): Show |
38 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1238-15832_1238-15 others(20): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827129 | CCACACAC others(17): Show |
C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0302 |
2 | HG02145.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1238-15842_1238-15 others(30): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45827129 | ||||||
| chr22:45827246 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-15745A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827246 | |||||||
| chr22:45827314 | C | T | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1238-15677C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827314 | |||||||
| chr22:45827358 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1238-15633G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827358 | |||||||
| chr22:45827463 | A | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02723.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-15528A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827463 | |||||||
| chr22:45827511 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1238-15480T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827511 | |||||||
| chr22:45827624 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1238-15367C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827624 | |||||||
| chr22:45827844 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG00738.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-15147A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45827844 | |||||||
| chr22:45828032 | A | C | 88 | a0001c0001t0001g0069 a0001c0001t0001g0088 a0001c0001t0001g0089 others(85): Show |
88 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1238-14959A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828032 | |||||||
| chr22:45828052 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1238-14939G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828052 | |||||||
| chr22:45828197 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1238-14794T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828197 | |||||||
| chr22:45828281 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1238-14710C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828281 | |||||||
| chr22:45828317 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-14674A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828317 | |||||||
| chr22:45828485 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1238-14506A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828485 | |||||||
| chr22:45828492 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-14499C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828492 | |||||||
| chr22:45828498 | T | C | 2 | a0001c0001t0008g0299 a0001c0001t0008g0301 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1238-14493T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828498 | |||||||
| chr22:45828574 | G | C | 10 | a0001c0001t0001g0270 a0001c0001t0001g0288 a0001c0001t0001g0293 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1238-14417G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828574 | |||||||
| chr22:45828681 | A | G | 16 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(13): Show |
16 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1238-14310A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828681 | |||||||
| chr22:45828735 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1238-14256G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828735 | |||||||
| chr22:45828750 | A | G | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-14241A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828750 | |||||||
| chr22:45828768 | A | G | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(14): Show |
17 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1238-14223A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828768 | |||||||
| chr22:45828951 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0297 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1238-14040C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828951 | |||||||
| chr22:45828983 | A | T | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1238-14008A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828983 | |||||||
| chr22:45828989 | A | G | 1 | a0001c0001t0007g0206 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1238-14002A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45828989 | |||||||
| chr22:45829070 | A | G | 7 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238-13921A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829070 | |||||||
| chr22:45829132 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-13859A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829132 | |||||||
| chr22:45829224 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1238-13767C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829224 | |||||||
| chr22:45829279 | C | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0001g0194 others(1): Show |
4 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-13712C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829279 | |||||||
| chr22:45829294 | C | G | 2 | a0001c0001t0005g0291 a0001c0001t0005g0292 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1238-13697C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829294 | |||||||
| chr22:45829339 | C | G | 1 | a0001c0001t0004g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1238-13652C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829339 | |||||||
| chr22:45829470 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1238-13521C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829470 | |||||||
| chr22:45829738 | C | T | 28 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1238-13253C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829738 | |||||||
| chr22:45829747 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1238-13244A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829747 | |||||||
| chr22:45829882 | A | T | 12 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0270 others(9): Show |
12 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1238-13109A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829882 | |||||||
| chr22:45829896 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-13095G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829896 | |||||||
| chr22:45829897 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
2 | NA18993.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1238-13094G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829897 | |||||||
| chr22:45829975 | A | T | 3 | a0001c0001t0001g0265 a0001c0001t0008g0299 a0001c0001t0008g0301 |
3 | HG03098.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1238-13016A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45829975 | |||||||
| chr22:45830694 | GA | G | 15 | a0001c0001t0001g0069 a0001c0001t0002g0108 a0001c0001t0003g0122 others(12): Show |
15 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1238-12283delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45830694 | ||||||
| chr22:45830746 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-12245A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45830746 | |||||||
| chr22:45830792 | C | T | 9 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0125 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1238-12199C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45830792 | |||||||
| chr22:45830990 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1238-12001A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45830990 | |||||||
| chr22:45831026 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1238-11965C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831026 | |||||||
| chr22:45831114 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1238-11877C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831114 | |||||||
| chr22:45831250 | G | T | 5 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-11741G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831250 | |||||||
| chr22:45831297 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1238-11694C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831297 | |||||||
| chr22:45831308 | A | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0134 a0001c0001t0002g0135 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-11683A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831308 | |||||||
| chr22:45831326 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1238-11665G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831326 | |||||||
| chr22:45831385 | T | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1238-11606T>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831385 | |||||||
| chr22:45831754 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1238-11237C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831754 | |||||||
| chr22:45831845 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1238-11146C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45831845 | |||||||
| chr22:45832018 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1238-10973C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832018 | |||||||
| chr22:45832038 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1238-10953A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832038 | |||||||
| chr22:45832080 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1238-10911A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832080 | |||||||
| chr22:45832100 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1238-10891A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832100 | |||||||
| chr22:45832170 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1238-10821G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832170 | |||||||
| chr22:45832291 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1238-10700A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832291 | |||||||
| chr22:45832320 | C | T | 27 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(24): Show |
27 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1238-10671C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832320 | |||||||
| chr22:45832346 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-10645C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832346 | |||||||
| chr22:45832347 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1238-10644G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832347 | |||||||
| chr22:45832551 | T | C | 1 | a0001c0001t0010g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1238-10440T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832551 | |||||||
| chr22:45832876 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1238-10115C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832876 | |||||||
| chr22:45832877 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0091 |
2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1238-10114G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832877 | |||||||
| chr22:45832981 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1238-10010T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832981 | |||||||
| chr22:45832992 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1238-9999G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45832992 | |||||||
| chr22:45833011 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1238-9980G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833011 | |||||||
| chr22:45833079 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1238-9912A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833079 | |||||||
| chr22:45833196 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1238-9795G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833196 | |||||||
| chr22:45833289 | T | G | 29 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1238-9702T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833289 | |||||||
| chr22:45833311 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1238-9680A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833311 | |||||||
| chr22:45833839 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0062 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1238-9152C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833839 | |||||||
| chr22:45833909 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1238-9082C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833909 | |||||||
| chr22:45833918 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-9073C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45833918 | |||||||
| chr22:45834000 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-8991C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834000 | |||||||
| chr22:45834011 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0155 |
2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1238-8980C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834011 | |||||||
| chr22:45834070 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-8921C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834070 | |||||||
| chr22:45834071 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
235 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.1238-8920T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834071 | |||||||
| chr22:45834121 | G | A | 1 | a0001c0001t0016g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1238-8870G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834121 | |||||||
| chr22:45834192 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1238-8799G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834192 | |||||||
| chr22:45834199 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1238-8792G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834199 | |||||||
| chr22:45834343 | G | T | 66 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0052 others(63): Show |
66 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1238-8648G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834343 | |||||||
| chr22:45834454 | G | A | 8 | a0001c0001t0001g0070 a0001c0001t0001g0165 a0001c0001t0001g0249 others(5): Show |
8 | HG00140.hp2 HG01168.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1238-8537G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834454 | |||||||
| chr22:45834500 | T | C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0293 a0001c0001t0014g0077 |
3 | HG01891.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1238-8491T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834500 | |||||||
| chr22:45834536 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1238-8455C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834536 | |||||||
| chr22:45834547 | A | G | 20 | a0001c0001t0001g0107 a0001c0001t0001g0130 a0001c0001t0001g0266 others(17): Show |
20 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1238-8444A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834547 | |||||||
| chr22:45834658 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1238-8333A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834658 | |||||||
| chr22:45834730 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1238-8261G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834730 | |||||||
| chr22:45834799 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0002g0121 |
3 | NA18944.hp1 NA18978.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1238-8192C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834799 | |||||||
| chr22:45834800 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238-8191G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834800 | |||||||
| chr22:45834834 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238-8157A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45834834 | |||||||
| chr22:45835057 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1238-7934C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835057 | |||||||
| chr22:45835265 | G | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0082 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1238-7726G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835265 | |||||||
| chr22:45835272 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1238-7719G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835272 | |||||||
| chr22:45835273 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1238-7718C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835273 | |||||||
| chr22:45835344 | G | A | 4 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0250 others(1): Show |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-7647G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835344 | |||||||
| chr22:45835508 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1238-7483C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835508 | |||||||
| chr22:45835524 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1238-7467G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835524 | |||||||
| chr22:45835543 | A | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-7448A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835543 | |||||||
| chr22:45835670 | T | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(3): Show |
6 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-7321T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835670 | |||||||
| chr22:45835742 | T | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0001g0193 others(3): Show |
6 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-7249T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835742 | |||||||
| chr22:45835743 | T | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0001g0193 others(3): Show |
6 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-7248T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835743 | |||||||
| chr22:45835903 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-7088A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835903 | |||||||
| chr22:45835937 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1238-7054A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45835937 | |||||||
| chr22:45836134 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1238-6857C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836134 | |||||||
| chr22:45836135 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1238-6856G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836135 | |||||||
| chr22:45836177 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1238-6814G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836177 | |||||||
| chr22:45836178 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1238-6813A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836178 | |||||||
| chr22:45836668 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1238-6323A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836668 | |||||||
| chr22:45836857 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1238-6134C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836857 | |||||||
| chr22:45837114 | CATATA | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-5871_1238-586 others(9): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45837114 | ||||||
| chr22:45837299 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0179 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1238-5692G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837299 | |||||||
| chr22:45837321 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-5670G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837321 | |||||||
| chr22:45837450 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0005g0071 a0001c0001t0005g0291 others(1): Show |
4 | HG02280.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-5541G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837450 | |||||||
| chr22:45837484 | A | G | 74 | a0001c0001t0001g0032 a0001c0001t0001g0088 a0001c0001t0001g0089 others(71): Show |
74 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1238-5507A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837484 | |||||||
| chr22:45837505 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0056 |
2 | NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1238-5486G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837505 | |||||||
| chr22:45837542 | G | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-5449G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837542 | |||||||
| chr22:45837614 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1238-5377C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837614 | |||||||
| chr22:45837721 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1238-5270G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837721 | |||||||
| chr22:45837746 | G | T | 1 | a0001c0001t0003g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1238-5245G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837746 | |||||||
| chr22:45837763 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0179 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1238-5228G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837763 | |||||||
| chr22:45837813 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-5178C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837813 | |||||||
| chr22:45837819 | A | G | 7 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG00738.hp2 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1238-5172A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837819 | |||||||
| chr22:45837824 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-5167T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837824 | |||||||
| chr22:45837862 | A | G | 26 | a0001c0001t0001g0092 a0001c0001t0002g0046 a0001c0001t0002g0090 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1238-5129A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837862 | |||||||
| chr22:45837889 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1238-5102A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45837889 | |||||||
| chr22:45838574 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1238-4417A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45838574 | |||||||
| chr22:45838606 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1238-4385C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45838606 | |||||||
| chr22:45838626 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1238-4365G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45838626 | |||||||
| chr22:45838724 | G | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-4267G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45838724 | |||||||
| chr22:45839067 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-3924A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839067 | |||||||
| chr22:45839205 | C | G | 1 | a0001c0001t0018g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1238-3786C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839205 | |||||||
| chr22:45839225 | C | T | 143 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(140): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1238-3766C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839225 | |||||||
| chr22:45839460 | C | T | 4 | a0001c0001t0006g0087 a0001c0001t0006g0119 a0001c0001t0006g0120 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-3531C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839460 | |||||||
| chr22:45839581 | A | C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(93): Show |
96 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1238-3410A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839581 | |||||||
| chr22:45839601 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1238-3390C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839601 | |||||||
| chr22:45839625 | A | G | 32 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1238-3366A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839625 | |||||||
| chr22:45839717 | A | T | 73 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0141 others(70): Show |
73 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1238-3274A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839717 | |||||||
| chr22:45839797 | A | G | 86 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0080 others(83): Show |
86 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1238-3194A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839797 | |||||||
| chr22:45839889 | T | C | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG00735.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1238-3102T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839889 | |||||||
| chr22:45840130 | A | G | 1 | a0001c0001t0015g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1238-2861A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840130 | |||||||
| chr22:45840148 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1238-2843A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840148 | |||||||
| chr22:45840309 | A | G | 39 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(36): Show |
39 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1238-2682A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840309 | |||||||
| chr22:45840335 | AAGAG | A | 25 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0070 others(22): Show |
25 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1238-2648_1238-264 others(8): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45840335 | ||||||
| chr22:45840363 | C | CAGCAGGT others(12): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(1): Show |
4 | NA18964.hp2 NA18985.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-2618_1238-260 others(23): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | 45840363 | ||||||
| chr22:45840449 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1238-2542G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840449 | |||||||
| chr22:45840545 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0067 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1238-2446G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840545 | |||||||
| chr22:45840579 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1238-2412G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840579 | |||||||
| chr22:45840685 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1238-2306G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840685 | |||||||
| chr22:45840972 | T | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0210 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1238-2019T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45840972 | |||||||
| chr22:45841028 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0003c0002t0001g0064 |
3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1238-1963G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841028 | |||||||
| chr22:45841063 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1238-1928G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841063 | |||||||
| chr22:45841122 | G | A | 19 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(16): Show |
19 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1238-1869G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841122 | |||||||
| chr22:45841350 | C | A | 6 | a0001c0001t0001g0271 a0001c0001t0004g0112 a0001c0001t0004g0113 others(3): Show |
6 | HG00642.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-1641C>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841350 | |||||||
| chr22:45841510 | G | T | 4 | a0001c0001t0006g0087 a0001c0001t0006g0119 a0001c0001t0006g0120 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1481G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841510 | |||||||
| chr22:45841560 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0295 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1238-1431C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841560 | |||||||
| chr22:45841561 | G | A | 1 | a0001c0001t0014g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1238-1430G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841561 | |||||||
| chr22:45841783 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1238-1208A>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841783 | |||||||
| chr22:45841784 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1207G>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45841784 | |||||||
| chr22:45842005 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1238-986G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842005 | |||||||
| chr22:45842189 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0080 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1238-802T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842189 | |||||||
| chr22:45842243 | T | C | 150 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0063 others(147): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1238-748T>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842243 | |||||||
| chr22:45842244 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238-747G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842244 | |||||||
| chr22:45842468 | A | G | 39 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(36): Show |
39 | HG00140.hp2 HG00408.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1238-523A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842468 | |||||||
| chr22:45842638 | G | A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG00642.hp2 HG02723.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1238-353G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842638 | |||||||
| chr22:45842849 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1238-142A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842849 | |||||||
| chr22:45842925 | G | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0144 a0001c0001t0001g0145 others(11): Show |
14 | HG02056.hp1 HG02155.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.1238-66G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842925 | |||||||
| chr22:45842958 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1238-33G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45842958 | |||||||
| chr22:45843208 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1425+30C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/11 | chr22 | 45843208 | |||||||
| chr22:45843246 | T | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1425+68T>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/11 | chr22 | 45843246 | |||||||
| chr22:45843436 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG02717.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1426-233A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/11 | chr22 | 45843436 | |||||||
| chr22:45843463 | G | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0134 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1426-206G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/11 | chr22 | 45843463 | |||||||
| chr22:45843541 | ATTGTTTT others(17): Show |
A | 1 | a0001c0001t0003g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1426-123_1426-100d others(26): Show |
ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | 45843541 |