Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 475 | 314 | 83 | 44 | 141 | 10 | 34 | 112 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0002 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0003 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1428 | 314 | 83 | 44 | 141 | 10 | 34 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| c0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| c0003 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1867 | 252 | 61 | 34 | 125 | 6 | 24 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0002 | 0/0 | 1867 | 30 | 5 | 5 | 13 | 3 | 4 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0003 | 0/0 | 1867 | 9 | 3 | 5 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0004 | 0/0 | 1867 | 5 | 0 | 0 | 0 | 0 | 5 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0005 | 0/0 | 1867 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0006 | 0/0 | 1867 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0007 | 0/0 | 1867 | 2 | 0 | 0 | 2 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0008 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0009 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0010 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0011 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0012 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0013 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0014 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0015 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0016 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0017 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| t0018 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 314 | 83 | 44 | 141 | 10 | 34 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0002c0003 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0003c0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | 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 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0002 | 0/0 | 3294 | 30 | 5 | 5 | 13 | 3 | 4 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0003 | 0/0 | 3294 | 9 | 3 | 5 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0004 | 0/0 | 3294 | 5 | 0 | 0 | 0 | 0 | 5 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0005 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0006 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0007 | 0/0 | 3294 | 2 | 0 | 0 | 2 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0008 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0009 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0010 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0011 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0012 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0013 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0014 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0015 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0016 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0017 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0001c0001t0018 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0002c0003t0001 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| a0003c0002t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | copy fasta | chr22 | 45666834 | 45850307 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0064 | 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 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0185 | 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 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0213 | 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 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0219 | 1/0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0291 | 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 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0115 | 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 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0002g0248 | 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 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0005g0070 | 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 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0006g0117 | 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 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0008g0302 | 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 |
| a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0014g0076 | 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 |
| a0001c0001t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0001c0001t0017g0246 | 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 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| a0003c0002t0001g0063 | 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 | g0281 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0181 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | GBR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0044 | 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 | g0190 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0151 | 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 | g0206 | EAS | CHS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0311 | 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 | g0022 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0272 | 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 | g0312 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0102 | 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 | g0101 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0127 | 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 | g0126 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0123 | 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 | g0064 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0315 | 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 | g0183 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0193 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02155 | hp1 | a0001 | c0001 | t0017 | g0246 | EAS | CDX | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0184 | 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 | g0067 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0135 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0301 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0106 | 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 | g0047 | 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 | g0074 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0300 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03225 | hp1 | a0003 | c0002 | t0001 | g0063 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0100 | 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 | g0294 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0080 | AFR | GWD | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0131 | 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 | g0139 | 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 | g0093 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0189 | 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 | g0179 | 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 | g0306 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | 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 | g0302 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0076 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | 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 | g0192 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0046 | 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 | g0169 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | 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 | g0050 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0053 | 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 | g0040 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | 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 | g0035 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | 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 | g0247 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0104 | 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 | g0027 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19000 | hp1 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0109 | 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 | g0265 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0057 | 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 | g0234 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0115 | 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 | g0196 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0042 | 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 | g0150 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | 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 | g0028 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ASW | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | TSI | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0095 | 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 | g0072 | AFR | ACB | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | MSL | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | USA | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0103 | AFR | LWK | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0219 | REF | REF | ATXN10_chr22_45666834_45850307 | ATXN10 | chr22 | 45666834 | 45850307 |
| 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 |
| 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 |
|---|
| 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 | a0001c0001t0006a0001c0001t0018 | 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 | a0001c0001t0006a0001c0001t0014 | 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 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(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 |
| 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 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 | a0001c0001t0001g0314 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0304a0001c0001t0001g0305 | 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 | a0001c0001t0001g0139a0001c0001t0004g0140 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0006g0117a0001c0001t0006g0119a0001c0001t0018g0118 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0304a0001c0001t0001g0305 | 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 | 76 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): 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 | a0001c0001t0001g0129a0001c0001t0001g0209a0001c0001t0001g0210others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0001g0203others(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 | a0001c0001t0005g0070 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0067 | 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 | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0084a0001c0001t0001g0085 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0066others(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 | a0001c0001t0001g0121a0001c0001t0002g0089a0001c0001t0003g0122others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0081a0001c0001t0001g0082 | 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 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0005g0292others(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 | a0001c0001t0001g0266a0001c0001t0011g0135 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0136a0001c0001t0001g0282 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0002g0212 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0266a0001c0001t0011g0135 | 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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0110others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0275 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0212 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0064 | 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 | 151 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): 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 | a0001c0001t0001g0274 | 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 | 256 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0055others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0048others(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 | 225 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0266a0001c0001t0011g0135 | 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 | a0001c0001t0001g0114a0001c0001t0001g0217a0001c0001t0001g0218others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0121a0001c0001t0002g0202a0001c0001t0003g0122others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0002g0153 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0275others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0202 | 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 | 246 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(243): 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0268 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0055others(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 | 240 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): 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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0091a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0142a0001c0001t0001g0220a0001c0001t0001g0221others(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 | 156 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0213a0001c0001t0014g0076 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0114a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0060others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0002g0202 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0213 | 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 | 67 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(64): 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0213a0001c0001t0001g0266a0001c0001t0001g0271others(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 | a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0005g0292 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0012g0080 | 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0005g0292 | 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 | a0001c0001t0007g0204a0001c0001t0007g0205 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0264others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(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 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0066others(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 | a0001c0001t0001g0121a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(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 | a0001c0001t0001g0067a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0196others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | 181 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0090others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0213 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0142a0001c0001t0001g0217a0001c0001t0001g0218others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0267a0001c0001t0001g0274 | 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 | a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | 247 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0007g0204a0001c0001t0007g0205 | 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 | a0001c0001t0006g0119 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | 77 | a0001c0001t0001g0007a0001c0001t0001g0141a0001c0001t0001g0143others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0001g0242others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(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 | a0001c0001t0001g0172a0001c0001t0003g0124a0001c0001t0003g0125others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0266a0001c0001t0011g0135 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0069others(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 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0064others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0109 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0139a0001c0001t0001g0241a0001c0001t0004g0140others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0082 | 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 | 70 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(67): 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0079others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0002g0093a0001c0001t0002g0100 | 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 | a0001c0001t0002g0093a0001c0001t0002g0100 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0002g0130a0001c0001t0002g0132a0001c0001t0002g0134others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0033a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0278 | 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 | 167 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0025others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0006g0086others(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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0001g0298a0001c0001t0012g0080 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0314 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0064a0001c0001t0001g0066 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0083a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0001t0001g0121a0001c0001t0002g0202a0001c0001t0003g0122others(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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0212 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0002g0130others(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 | a0001c0001t0001g0090a0001c0001t0001g0241 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0212 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 |
310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | |||||
| chr22:45706698
|
G | GTTTATTT others(23): Show |
5 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | 22 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(19): Show | 22 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(19): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0121a0001c0001t0002g0202a0001c0001t0003g0122others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0081a0001c0001t0001g0082 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0129a0001c0001t0001g0213a0001c0001t0002g0130others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0166a0001c0001t0001g0174 | 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 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0001g0189 | 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 | a0001c0001t0001g0129a0001c0001t0001g0213a0001c0001t0002g0130others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | 205 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | 195 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.648-7215G>C | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45711198 | ||||||
| chr22:45711225
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): 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 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0094 | 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 | 78 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0141others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): 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 | a0002c0003t0001g0184 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0051 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0274 | 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 | a0001c0001t0001g0136a0001c0001t0001g0282 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0282a0001c0001t0001g0296a0001c0001t0001g0297others(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 | a0001c0001t0008g0300a0001c0001t0008g0302a0001c0001t0016g0301 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0121a0001c0001t0001g0271a0001c0001t0003g0122others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0001g0068 | 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 | 76 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.648-3135delA | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 5/11 | chr22 | 45715277 | ||||||
| chr22:45715558
|
G | C | 6 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0129a0001c0001t0001g0213a0001c0001t0002g0130others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0043others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0185a0001c0001t0001g0191 | 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 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0050others(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 | a0001c0001t0003g0127a0001c0001t0003g0128 | 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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0067 | 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 | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): 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 | a0001c0001t0007g0204a0001c0001t0007g0205 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0236others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0150a0001c0001t0001g0266a0001c0001t0001g0289others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0108others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): 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 | a0001c0001t0006g0086a0001c0001t0006g0117a0001c0001t0006g0119others(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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0002g0045 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0295 | 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 | 70 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(67): 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0002g0120others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0106a0001c0001t0002g0094a0001c0001t0002g0099others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0002g0092 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0136a0001c0001t0001g0282a0001c0001t0001g0298 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0136a0001c0001t0001g0282a0001c0001t0001g0289others(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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0283others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0002g0202 | 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 | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0083others(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 | a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0068a0001c0001t0001g0282a0001c0001t0001g0283others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0002g0045 | 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 | a0001c0001t0001g0143a0001c0001t0001g0148 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | 2 | a0001c0001t0001g0157a0001c0001t0001g0266 | 2 | NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.729-2971A>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 6/11 | chr22 | 45726454 | ||||||
| chr22:45726455
|
T | C | 1 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0019others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0082 | 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 |
15 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0026others(12): Show | 15 | HG00140.hp2 HG02135.hp1 HG02897.hp1 others(12): 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 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0176 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0047others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0266a0001c0001t0002g0202 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0314 | 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 | a0001c0001t0001g0121a0001c0001t0003g0124 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0129a0001c0001t0001g0213a0001c0001t0002g0130others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0083others(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 | a0001c0001t0002g0099a0001c0001t0002g0105 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0212 | 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 | a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0002g0248 | 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 | a0001c0001t0001g0014a0001c0001t0001g0067a0001c0001t0001g0084others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0107a0001c0001t0002g0120 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0264 | 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 | a0001c0001t0002g0202 | 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 | 85 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(82): 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 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0079others(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 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0067others(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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0237a0001c0001t0001g0240 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0006g0117a0001c0001t0006g0119a0001c0001t0018g0118 | 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 | 93 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0114others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(90): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0057a0001c0001t0001g0059 | 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 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(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 | a0001c0001t0001g0218a0001c0001t0001g0303 | 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 | 81 | a0001c0001t0001g0031a0001c0001t0001g0114a0001c0001t0001g0141others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(78): 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 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0314 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0005g0292others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0001t0001g0186others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0139a0001c0001t0004g0140a0001c0001t0004g0244 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0062others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(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 | a0001c0001t0001g0069a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0129a0001c0001t0001g0213a0001c0001t0002g0130others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0110 | 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 | a0001c0001t0001g0037a0001c0001t0001g0218a0001c0001t0001g0265others(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 | 46 | a0001c0001t0001g0031a0001c0001t0001g0077a0001c0001t0001g0090others(43): Show | 46 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(43): 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 | 147 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0078others(144): 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 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0072others(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 | a0001c0001t0001g0079a0001c0001t0001g0209a0001c0001t0001g0274 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0003c0002t0001g0063 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0006g0117a0001c0001t0006g0119a0001c0001t0018g0118 | 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 | a0001c0001t0005g0293 | 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 | 198 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): 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 | a0001c0001t0005g0292 | 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 | a0001c0001t0012g0080 | 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 | a0001c0001t0001g0289a0001c0001t0001g0296 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0294others(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 | 93 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0072others(90): 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 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0016 | 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 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0082others(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 | 145 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0062others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): 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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | 87 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0084others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0282a0001c0001t0001g0289a0001c0001t0001g0290others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0272a0001c0001t0006g0086 | 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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0081a0001c0001t0001g0082 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0136a0001c0001t0001g0289a0001c0001t0001g0290others(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 | a0001c0001t0001g0121a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0296 | 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 | 254 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0062others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0298a0001c0001t0012g0080 | 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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0106others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0044 | 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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0287 | 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 | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0002g0107a0001c0001t0002g0120 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0001g0005a0001c0001t0001g0016 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068a0001c0001t0001g0271 | 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 | 145 | a0001c0001t0001g0064a0001c0001t0001g0084a0001c0001t0001g0114others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0209 | 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 | 72 | a0001c0001t0001g0048a0001c0001t0001g0137a0001c0001t0001g0138others(69): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(258): 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0079others(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 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0071others(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 | a0001c0001t0001g0042 | 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 | 127 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(124): Show | 127 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(124): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0001t0001g0068a0001c0001t0001g0129a0001c0001t0001g0273others(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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0078others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0091a0001c0001t0001g0159a0001c0001t0001g0272others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0013a0001c0001t0001g0114 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0139a0001c0001t0001g0241a0001c0001t0004g0140others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0081 | 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 | 152 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(149): 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 | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0236others(1): Show | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 163 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | 147 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(144): 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0091a0001c0001t0002g0113 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0067a0001c0001t0001g0266a0001c0001t0008g0300others(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 | 148 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(145): 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | 146 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(143): 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 | a0001c0001t0001g0136a0001c0001t0001g0253a0001c0001t0007g0204others(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 | a0001c0001t0001g0287 | 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0001t0001g0187others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0079 | 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 | a0001c0001t0001g0271a0001c0001t0001g0297a0001c0001t0003g0125others(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 | a0001c0001t0001g0129a0001c0001t0001g0209a0001c0001t0001g0266others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0067others(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 | 80 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(77): Show | 80 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(77): 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0253a0001c0001t0007g0204a0001c0001t0007g0205 | 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 | 112 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0071others(109): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0114a0001c0001t0002g0100a0001c0001t0004g0111others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0137a0001c0001t0001g0210a0001c0001t0001g0211others(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 | 64 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0138others(61): 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 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0072others(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 | 149 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0062others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(146): 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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0159others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0077a0001c0001t0001g0136a0001c0001t0001g0294others(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 | a0001c0001t0001g0121a0001c0001t0001g0295 | 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 | a0001c0001t0001g0078a0001c0001t0001g0090 | 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 | a0001c0001t0001g0085a0001c0001t0005g0292 | 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 | a0001c0001t0002g0094a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0002g0099a0001c0001t0002g0105 | 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 | a0001c0001t0002g0098a0001c0001t0002g0153 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0010g0103 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0002g0093a0001c0001t0002g0100a0001c0001t0002g0104 | 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 | a0001c0001t0002g0089a0001c0001t0002g0108 | 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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0002g0109 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0045a0001c0001t0002g0092 | 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 | a0001c0001t0002g0115a0001c0001t0002g0248 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0011a0001c0001t0001g0014 | 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 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0253others(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 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0002g0094others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | 167 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(164): 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 | a0001c0001t0001g0180a0001c0001t0001g0194 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0314 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0141others(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 | 100 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0091others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0047others(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 | a0001c0001t0001g0064a0001c0001t0001g0066 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0213a0001c0001t0001g0298 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0278 | 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 | 75 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0138others(72): 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 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | 178 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(175): 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0283a0001c0001t0001g0285a0001c0001t0001g0286 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0008g0300 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0091others(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 | a0001c0001t0001g0058a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0067others(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 | a0001c0001t0001g0068a0001c0001t0001g0161a0001c0001t0001g0193others(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 | a0001c0001t0001g0138a0001c0001t0001g0142a0001c0001t0001g0147others(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 | 105 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(102): 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 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0001g0266 | 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 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0062others(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 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0084others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0078others(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 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0129others(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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0224a0001c0001t0001g0262 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0091a0001c0001t0002g0113 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | 187 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(184): Show | 187 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(184): 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 | a0001c0001t0003g0124 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0129others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0162a0001c0001t0001g0178 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0143others(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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | 179 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1173+15462C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45756000 | ||||||
| chr22:45756075
|
C | G | 246 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | 213 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0091a0001c0001t0001g0161a0001c0001t0002g0045others(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 | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0254others(4): 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135others(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 | a0001c0001t0002g0212a0001c0001t0005g0070a0001c0001t0014g0076 | 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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0082others(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 | a0001c0001t0001g0295 | 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 | a0001c0001t0010g0103 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0002g0094a0001c0001t0002g0099a0001c0001t0002g0105others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | 151 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(148): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0202 | 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 | 69 | a0001c0001t0001g0114a0001c0001t0001g0141a0001c0001t0001g0143others(66): Show | 69 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(66): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0160others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | 73 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0138others(70): 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0013g0018 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0071 | 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 | 224 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0266a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0266a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0186others(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 | a0001c0001t0002g0202 | 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 | 153 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0081others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(150): 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0002g0202 | 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 | 224 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0067a0001c0001t0001g0266 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | 180 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(177): 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0078others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | 151 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(148): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0121others(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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0013a0001c0001t0001g0067a0001c0001t0012g0080 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0010g0103 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0010g0103 | 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 | 156 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(153): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | a0001c0001t0002g0202a0001c0001t0002g0212a0001c0001t0005g0070others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0078others(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 | a0001c0001t0001g0213a0001c0001t0001g0298 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0067a0001c0001t0012g0080 | 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 | a0001c0001t0001g0271 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0067a0001c0001t0012g0080 | 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 | a0001c0001t0001g0139a0001c0001t0004g0140a0001c0001t0004g0225others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0072others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135others(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 | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0120 | 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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0198a0001c0001t0001g0201 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0280others(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 | a0001c0001t0002g0202 | 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 | 253 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135 | 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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0172a0001c0001t0001g0299 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0251others(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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0289 | 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 | a0001c0001t0005g0292 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | 94 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(91): 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 | a0001c0001t0001g0194a0001c0001t0001g0238a0001c0001t0001g0307others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0016g0301 | 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 | |||||
| chr22:45773445
|
ATTATTTA others(1): Show |
A | 3 | a0001c0001t0001g0157a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG01069.hp1 HG02300.hp2 homoSapiens_chm13v2.hp1 |
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 | |||||
| chr22:45773484
|
T | G | 247 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0006g0086a0001c0001t0006g0117a0001c0001t0006g0119others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0231a0001c0001t0002g0153 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0169a0001c0001t0001g0187 | 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 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0067a0001c0001t0001g0266 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0251others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | 3 | a0001c0001t0001g0157a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG01069.hp1 HG02300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1174-30551C>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45776408 | ||||||
| chr22:45776449
|
A | T | 1 | a0001c0001t0003g0308 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0278a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0278a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0278a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0091a0001c0001t0001g0298a0001c0001t0002g0045others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | 236 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(233): Show | 236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0005g0070 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0149 | 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 | 205 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(202): Show | 205 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(202): 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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0217a0001c0001t0001g0256a0001c0001t0001g0257others(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 | a0001c0001t0002g0212a0001c0001t0005g0070a0001c0001t0014g0076 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0082others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0001g0170others(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 | a0001c0001t0001g0297 | 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 | 74 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0138others(71): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | 247 | a0001c0001t0001g0037a0001c0001t0001g0061a0001c0001t0001g0062others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | a0001c0001t0001g0067 | 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 | 32 | a0001c0001t0001g0091a0001c0001t0001g0214a0001c0001t0001g0215others(29): 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 | a0001c0001t0006g0086a0001c0001t0006g0117a0001c0001t0006g0119others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0060 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0127others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0158a0001c0001t0001g0207 | 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 | 67 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(64): Show | 67 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(64): 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0129a0001c0001t0001g0268a0001c0001t0001g0269others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0138 | 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 | 67 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0141others(64): Show | 67 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(64): 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0006g0117a0001c0001t0006g0119a0001c0001t0018g0118 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | 191 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(188): Show | 191 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(188): 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 | a0001c0001t0001g0139a0001c0001t0004g0244a0001c0001t0007g0204 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0304 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1174-22332G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784627 | ||||||
| chr22:45784690
|
C | G | 1 | a0001c0001t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1174-22269C>G | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45784690 | ||||||
| chr22:45784707
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0082others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0276a0001c0001t0001g0314 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | 68 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(65): Show | 68 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1174-20083G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 9/11 | chr22 | 45786876 | ||||||
| chr22:45786912
|
C | T | 213 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(210): 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0172a0001c0001t0001g0183a0001c0001t0001g0299 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0068a0001c0001t0002g0130a0001c0001t0002g0131others(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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0002g0248 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0176 | 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 | a0001c0001t0002g0045a0001c0001t0002g0089a0001c0001t0002g0097others(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 | a0001c0001t0001g0067a0001c0001t0012g0080 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0068a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0143a0001c0001t0001g0148 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0023others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 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 | a0001c0001t0011g0135 | 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 | 147 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0087others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(144): 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 | a0001c0001t0001g0083a0001c0001t0001g0316 | 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 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(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 | 251 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(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 | 248 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0012g0080 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0055 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0306 | 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 | a0001c0001t0002g0202 | 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 | 248 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): 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 | a0001c0001t0006g0117 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0245a0001c0001t0001g0251 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0049a0001c0001t0001g0055 | 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 | a0001c0001t0001g0013 | 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 | 246 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0002g0202a0001c0001t0002g0212a0001c0001t0003g0122others(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 | a0001c0001t0001g0180a0001c0001t0001g0218a0001c0001t0001g0307 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0002g0212a0001c0001t0005g0070a0001c0001t0014g0076 | 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 | 153 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0087others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(150): 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0002g0212a0001c0001t0005g0070a0001c0001t0014g0076 | 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 | a0001c0001t0001g0068a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0068a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0050others(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 | a0001c0001t0001g0139a0001c0001t0001g0166a0001c0001t0001g0174others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0213a0001c0001t0001g0298 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0315 | 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 | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0034others(34): Show | 37 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(34): 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 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0087others(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 | a0001c0001t0001g0088a0001c0001t0001g0142a0001c0001t0001g0144others(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 | a0001c0001t0001g0152a0001c0001t0001g0307a0001c0001t0002g0107 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(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 | 46 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0017others(43): 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 | a0001c0001t0001g0055a0001c0001t0001g0084a0001c0001t0001g0121others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0147a0001c0001t0001g0150 | 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 | a0001c0001t0001g0266a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0002g0109 | 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 | a0001c0001t0002g0045a0001c0001t0002g0092a0001c0001t0002g0105 | 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 | a0001c0001t0001g0091a0001c0001t0002g0089a0001c0001t0002g0113 | 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 | a0001c0001t0002g0093a0001c0001t0002g0104a0001c0001t0002g0115 | 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 | a0001c0001t0002g0094a0001c0001t0002g0097a0001c0001t0002g0099others(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 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0108others(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 | a0001c0001t0002g0153a0001c0001t0010g0103 | 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 | a0001c0001t0002g0096a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0002g0100 | 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 | a0001c0001t0002g0100 | 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 | a0001c0001t0002g0100 | 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 | a0001c0001t0016g0301 | 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 | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | a0001c0001t0001g0172a0001c0001t0001g0299 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0289others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0003g0122 | 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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0185others(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 | a0001c0001t0001g0067a0001c0001t0001g0141 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | 132 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(129): 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 | 100 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0091others(97): 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 | a0001c0001t0001g0154a0001c0001t0001g0258a0001c0001t0001g0259others(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 | a0001c0001t0008g0302 | 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 | 239 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0266a0001c0001t0008g0302 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0213 | 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 | 237 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0120 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0192 | 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 | 250 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0077others(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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(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 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0058others(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 | 226 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): 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 | a0001c0001t0001g0162a0001c0001t0001g0178 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | 252 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0003g0127a0001c0001t0003g0128 | 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | 72 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0114others(69): Show | 72 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(69): 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 | a0001c0001t0001g0267a0001c0001t0001g0274 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0008g0300 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0256a0001c0001t0001g0257 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0143a0001c0001t0001g0148 | 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0314 | 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 | a0001c0001t0001g0142a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0001t0010g0103 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | 73 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0114others(70): Show | 73 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(70): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0068a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0017g0246 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0002g0045a0001c0001t0002g0089a0001c0001t0002g0097others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0007g0204 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0077a0001c0001t0001g0079 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | 2 | a0001c0001t0001g0157a0001c0001t0001g0305 | 2 | HG01069.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0162a0001c0001t0001g0178 | 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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0001g0068a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0129a0001c0001t0001g0269 | 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 | a0001c0001t0002g0212a0001c0001t0005g0070 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0001g0067a0001c0001t0012g0080 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0001g0049 | 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 | 253 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0062others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0159a0001c0001t0001g0217a0001c0001t0001g0218others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0130others(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 | 149 | a0001c0001t0001g0071a0001c0001t0001g0087a0001c0001t0001g0088others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(146): 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | a0001c0001t0001g0279a0001c0001t0002g0130a0001c0001t0002g0131others(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 | 212 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0058others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): 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 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0003g0124a0001c0001t0003g0308 | 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 | a0001c0001t0001g0067a0001c0001t0001g0078a0001c0001t0001g0266others(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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0001g0194a0001c0001t0001g0253 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0316 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0129a0001c0001t0001g0268a0001c0001t0001g0269others(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 | a0001c0001t0001g0166a0001c0001t0001g0174 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0194a0001c0001t0001g0253 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0003g0122others(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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | a0001c0001t0003g0127a0001c0001t0003g0128 | 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 | a0001c0001t0001g0067a0001c0001t0001g0266a0001c0001t0008g0300others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(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 | 187 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0173others(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 | a0001c0001t0002g0108a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0058others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0068a0001c0001t0001g0271a0001c0001t0001g0297others(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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0114others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209others(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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0045others(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 | 250 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0001c0001t0001g0068a0001c0001t0001g0271a0001c0001t0001g0297others(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 | a0001c0001t0004g0111a0001c0001t0004g0112 | 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 | 73 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(70): Show | 73 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(70): 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 | a0001c0001t0001g0271a0001c0001t0001g0297 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0021a0001c0001t0001g0060 | 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 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0067a0001c0001t0001g0068 | 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 | a0001c0001t0001g0296 | 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 | 35 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(32): Show | 35 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(32): 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 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0147others(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 | a0001c0001t0001g0071a0001c0001t0001g0087a0001c0001t0001g0088others(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 | 71 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(68): 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 | a0001c0001t0001g0250a0001c0001t0001g0271a0001c0001t0001g0297 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0271a0001c0001t0001g0297 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0267a0001c0001t0001g0274 | 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 | 256 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0143a0001c0001t0001g0148 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0298a0001c0001t0012g0080 | 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 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0217others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0047others(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 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0196others(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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0290others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0001g0068a0001c0001t0006g0086a0001c0001t0006g0117others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0067a0001c0001t0001g0266a0001c0001t0008g0300others(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 | a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0045others(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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0029others(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 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0068others(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 | a0001c0001t0001g0091a0001c0001t0001g0269a0001c0001t0001g0270others(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 | 151 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0260a0001c0001t0001g0261 | 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 | a0001c0001t0002g0089 | 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 | a0001c0001t0001g0297 | 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 | 87 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(84): Show | 87 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(84): 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(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 | a0001c0001t0001g0064a0001c0001t0001g0066 | 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 | a0001c0001t0001g0068a0001c0001t0002g0202a0001c0001t0006g0086others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0042 | 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 | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0006g0086 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0001t0001g0186others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0213a0001c0001t0001g0298a0001c0001t0011g0135others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0067a0001c0001t0001g0266a0001c0001t0008g0300others(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 | a0001c0001t0002g0202 | 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 | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0067a0001c0001t0001g0266a0001c0001t0008g0300others(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 | a0001c0001t0001g0068a0001c0001t0003g0122a0001c0001t0003g0123others(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 | a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0081a0001c0001t0001g0278 | 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 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0110 | 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 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(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 | a0001c0001t0001g0052a0001c0001t0001g0283a0001c0001t0001g0285 | 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 | a0001c0001t0001g0048a0001c0001t0001g0078a0001c0001t0001g0159others(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 | 18 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0176others(15): Show | 18 | HG00673.hp1 HG01069.hp1 HG01106.hp1 others(15): 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 | 162 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0081others(159): 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(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 | a0001c0001t0001g0217a0001c0001t0001g0303 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0129a0001c0001t0001g0268a0001c0001t0001g0269others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | 89 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0088others(86): Show | 89 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(86): 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 | a0001c0001t0011g0135 | 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 | 251 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0271a0001c0001t0001g0289a0001c0001t0001g0294others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0213a0001c0001t0001g0298 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0007g0204 | 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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0193others(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 | a0001c0001t0005g0292a0001c0001t0005g0293 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0271others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0024a0001c0001t0001g0026 | 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 | a0001c0001t0001g0266a0001c0001t0008g0300a0001c0001t0008g0302 | 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 | a0001c0001t0001g0068a0001c0001t0002g0107a0001c0001t0003g0122others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(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 | a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0130a0001c0001t0002g0132a0001c0001t0002g0134others(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 | a0001c0001t0001g0013 | 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 | 247 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0010g0103 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0061a0001c0001t0001g0090 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0029 | 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 | 230 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0062others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0094a0001c0001t0002g0153 | 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 | a0001c0001t0002g0202 | 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 236 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(233): 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 | a0001c0001t0016g0301 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0199 | 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 | 67 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0051others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0001c0001t0001g0069a0001c0001t0001g0164a0001c0001t0001g0250others(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 | a0001c0001t0001g0064a0001c0001t0001g0294a0001c0001t0014g0076 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0001g0267others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0002g0120 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0180 | 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 | 75 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0129others(72): 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 | a0001c0001t0001g0290a0001c0001t0001g0291 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0251others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0192others(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 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0192others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0306 | 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 | 3 | a0001c0001t0001g0157a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG01069.hp1 HG02300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1238-6814G>A | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45836177 | ||||||
| chr22:45836178
|
A | G | 1 | a0001c0001t0003g0124 | 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 | a0001c0001t0001g0087a0001c0001t0001g0088 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0162a0001c0001t0001g0178 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0289a0001c0001t0005g0070a0001c0001t0005g0292others(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 | 75 | a0001c0001t0001g0031a0001c0001t0001g0087a0001c0001t0001g0088others(72): Show | 75 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(72): 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 | a0001c0001t0001g0049a0001c0001t0001g0055 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0064a0001c0001t0001g0066 | 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 | a0001c0001t0003g0122 | 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 | a0001c0001t0001g0162a0001c0001t0001g0178 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0091a0001c0001t0002g0045a0001c0001t0002g0089others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0003g0181 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | 144 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0062others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): 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 | a0001c0001t0006g0086a0001c0001t0006g0117a0001c0001t0006g0119others(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 | 97 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0062others(94): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(94): 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 | a0001c0001t0003g0125 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | 74 | a0001c0001t0001g0031a0001c0001t0001g0114a0001c0001t0001g0139others(71): Show | 74 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1238-3274A>T | ATXN10 | ENSG00000130638.18 | transcript | ENST00000252934.10 | protein_coding | 10/11 | chr22 | 45839717 | ||||||
| chr22:45839797
|
A | G | 87 | a0001c0001t0001g0031a0001c0001t0001g0068a0001c0001t0001g0079others(84): Show | 87 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(84): 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 | a0001c0001t0003g0125a0001c0001t0003g0126 | 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 | a0001c0001t0001g0294a0001c0001t0001g0295 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(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 | a0001c0001t0001g0210 | 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 | 102 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(99): 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0209others(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 | a0001c0001t0001g0062a0001c0001t0001g0065a0003c0002t0001g0063 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0272a0001c0001t0004g0111a0001c0001t0004g0112others(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 | a0001c0001t0006g0086a0001c0001t0006g0117a0001c0001t0006g0119others(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 | a0001c0001t0001g0079a0001c0001t0001g0296 | 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 | a0001c0001t0014g0076 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0002g0100 | 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 | 84 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0081others(81): 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 | 151 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0062others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0001g0129a0001c0001t0001g0268a0001c0001t0001g0269others(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 | a0001c0001t0001g0031a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0001g0078a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(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 | a0001c0001t0003g0308 | 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 |