Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9576 |
|---|---|
| ensemblid | ENSG00000077327.16 |
| hgncid | 11215 |
| symbol | SPAG6 |
| name | sperm associated antigen 6 |
| refseq_nuc | NM_012443.4 |
| refseq_prot | NP_036575.1 |
| ensembl_nuc | ENST00000376624.8 |
| ensembl_prot | ENSP00000365811.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 22345496 |
| end | 22417610 |
| strand | + |
| ver | v1.2 |
| region | chr10:22345496-22417610 |
| region5000 | chr10:22340496-22422610 |
| regionname0 | SPAG6_chr10_22345496_22417610 |
| regionname5000 | SPAG6_chr10_22340496_22422610 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1530 | 80 | 29 | 22 | 14 | 6 | 7 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| c0002 | 0/0 | 1530 | 61 | 49 | 10 | 0 | 0 | 2 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| c0003 | 0/0 | 1530 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1039 | 98 | 49 | 21 | 12 | 6 | 8 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0002 | 0/0 | 1039 | 20 | 12 | 7 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0003 | 0/0 | 1039 | 11 | 9 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0004 | 0/0 | 1039 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0005 | 0/0 | 1039 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0006 | 0/0 | 1039 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0007 | 0/0 | 1039 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0008 | 0/0 | 1039 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| t0009 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1530 | 80 | 29 | 22 | 14 | 6 | 7 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0001c0003 | 0/0 | 1530 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002 | 0/0 | 1530 | 61 | 49 | 10 | 0 | 0 | 2 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2568 | 75 | 27 | 21 | 12 | 6 | 7 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0001c0001t0005 | 0/0 | 2568 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0001c0001t0007 | 0/0 | 2568 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0001c0003t0001 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0001 | 0/0 | 2568 | 22 | 22 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0002 | 0/0 | 2568 | 20 | 12 | 7 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0003 | 0/0 | 2568 | 11 | 9 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0004 | 0/0 | 2568 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0006 | 0/0 | 2568 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0008 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| a0002c0002t0009 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | copy fasta | chr10 | 22340496 | 22422610 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0008g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| a0002c0002t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0129 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0107 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0131 | AMR | PUR | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0133 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0115 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PEL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0130 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0116 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02602 | hp1 | a0002 | c0002 | t0008 | g0007 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02723 | hp2 | a0002 | c0002 | t0006 | g0100 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0114 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0086 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0113 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03098 | hp2 | a0002 | c0002 | t0006 | g0053 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0128 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0132 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0111 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0112 | AFR | ESN | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0125 | AFR | MSL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0137 | SAS | BEB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0043 | SAS | BEB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18522 | hp1 | a0002 | c0002 | t0009 | g0017 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | LWK | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0126 | AFR | LWK | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | YRI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ASW | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0103 | AFR | ACB | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | USA | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | USA | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0050 | REF | REF | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | SPAG6_chr10_22340496_22422610 | SPAG6 | chr10 | 22340496 | 22422610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:22386928
|
A | G | 1 | a0002 | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
missense_variant | MODERATE | c.647A>G | p.Gln216Arg | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 5/11 | 763/2568 | 647/1530 | 216/509 | chr10 | 22386928 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:22391734
|
A | G | 1 | a0001c0003 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.1011A>G | p.Val337Val | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/11 | 1127/2568 | 1011/1530 | 337/509 | chr10 | 22391734 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:22345584
|
G | A | 1 | a0002c0002t0008 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-28G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 1/11 | 28 | chr10 | 22345584 | |||||
| chr10:22416846
|
C | T | 3 | a0002c0002t0002a0002c0002t0003a0002c0002t0006 | 34 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*158C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 158 | chr10 | 22416846 | |||||
| chr10:22416847
|
G | A | 1 | a0002c0002t0009 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 159 | chr10 | 22416847 | |||||
| chr10:22417097
|
T | C | 1 | a0002c0002t0004 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 409 | chr10 | 22417097 | |||||
| chr10:22417268
|
T | A | 1 | a0002c0002t0006 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 580 | chr10 | 22417268 | |||||
| chr10:22417346
|
G | A | 1 | a0001c0001t0005 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*658G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 658 | chr10 | 22417346 | |||||
| chr10:22417381
|
A | T | 1 | a0001c0001t0007 | 2 | NA18957.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 693 | chr10 | 22417381 | |||||
| chr10:22417457
|
C | T | 1 | a0002c0002t0003 | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*769C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 769 | chr10 | 22417457 | |||||
| chr10:22417573
|
G | A | 1 | a0001c0001t0005 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*885G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 11/11 | 885 | chr10 | 22417573 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:22346000
|
T | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+182T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346000 | ||||||
| chr10:22346013
|
G | A | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+195G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346013 | ||||||
| chr10:22346112
|
C | G | 1 | a0002c0002t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.121+294C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346112 | ||||||
| chr10:22346164
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.121+346C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346164 | ||||||
| chr10:22346238
|
G | C | 1 | a0002c0002t0002g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.121+420G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346238 | ||||||
| chr10:22346393
|
C | T | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+575C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346393 | ||||||
| chr10:22346430
|
G | GTTC | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0073others(13): Show | 18 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.121+678_121+680dup others(3): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
G | GTTCTTC | 20 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(17): Show | 20 | HG00738.hp2 HG01515.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.121+675_121+680dup others(6): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
G | GTTCTTCT others(2): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 13 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.121+672_121+680dup others(9): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
G | GTTCTTCT others(5): Show |
13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 13 | HG01255.hp1 HG01256.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.121+669_121+680dup others(12): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
G | GTTCTTCT others(8): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01934.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.121+666_121+680dup others(15): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
G | GTTCTTCT others(11): Show |
1 | a0001c0001t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.121+663_121+680dup others(18): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
GTTC | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 9 | HG01175.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+678_121+680del others(3): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
GTTCTTC | G | 6 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02717.hp2 HG03098.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+675_121+680del others(6): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346430
|
GTTCTTCT others(5): Show |
G | 2 | a0001c0001t0001g0127a0002c0002t0008g0007 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.121+669_121+680del others(12): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346430 | |||||
| chr10:22346463
|
CTTCTTCT others(27): Show |
C | 1 | a0002c0002t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.121+661_121+694del others(34): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346463 | |||||
| chr10:22346467
|
TTCTTCTT others(26): Show |
T | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+651_121+683del others(33): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346467 | |||||
| chr10:22346469
|
CTTCTTCT others(21): Show |
C | 2 | a0002c0002t0001g0015a0002c0002t0001g0016 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.121+667_121+694del others(28): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346469 | |||||
| chr10:22346479
|
TTCTTCTT others(4): Show |
T | 1 | a0002c0002t0003g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.121+663_121+673del others(11): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346479 | |||||
| chr10:22346482
|
TTCTTCTT others(1): Show |
T | 2 | a0002c0002t0003g0131a0002c0002t0003g0132 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.121+666_121+673del others(8): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346482 | |||||
| chr10:22346484
|
CTTCTTCT others(6): Show |
C | 2 | a0002c0002t0001g0018a0002c0002t0009g0017 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.121+681_121+693del others(13): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346484 | |||||
| chr10:22346485
|
TTCTTC | T | 3 | a0002c0002t0003g0128a0002c0002t0003g0129a0002c0002t0003g0130 | 3 | HG01192.hp2 HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.121+669_121+673del others(5): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346485 | |||||
| chr10:22346487
|
CTTCTTCT others(3): Show |
C | 3 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021 | 3 | HG02559.hp1 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+681_121+690del others(10): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346487 | |||||
| chr10:22346488
|
TTC | T | 2 | a0002c0002t0003g0125a0002c0002t0004g0126 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.121+672_121+673del others(2): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346488 | |||||
| chr10:22346490
|
C | CT | 2 | a0001c0001t0005g0123a0002c0002t0002g0124 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121+674dupT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346490 | |||||
| chr10:22346490
|
C | CTTCT | 7 | a0002c0002t0002g0013a0002c0002t0002g0116a0002c0002t0003g0111others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+674_121+677dup others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346490 | |||||
| chr10:22346490
|
C | CTTCTTCT others(3): Show |
2 | a0002c0002t0002g0087a0002c0002t0004g0086 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.121+680_121+681ins others(10): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346490 | |||||
| chr10:22346490
|
C | CTTCTTCT others(42): Show |
1 | a0001c0001t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.121+680_121+681ins others(49): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346490 | |||||
| chr10:22346490
|
C | CTTCTTCT others(39): Show |
1 | a0001c0001t0001g0088 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.121+691_121+736dup others(46): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346490 | |||||
| chr10:22346493
|
CTTCT | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0024 | 3 | HG02486.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.121+681_121+684del others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346493 | |||||
| chr10:22346497
|
T | TTC | 2 | a0001c0001t0001g0026a0002c0002t0001g0025 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.121+680_121+681ins others(2): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346497 | |||||
| chr10:22346497
|
T | TTCTTC | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | HG01192.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.121+680_121+681ins others(5): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346497 | |||||
| chr10:22346497
|
T | TTCTTCTT others(4): Show |
1 | a0001c0001t0001g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.121+680_121+681ins others(11): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346497 | |||||
| chr10:22346497
|
T | TTCTTCTT others(7): Show |
1 | a0002c0002t0001g0134 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.121+680_121+681ins others(14): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22346497 | |||||
| chr10:22346499
|
T | C | 1 | a0002c0002t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+681T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346499 | ||||||
| chr10:22346500
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+682C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346500 | ||||||
| chr10:22346513
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.121+695C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346513 | ||||||
| chr10:22346613
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+795G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346613 | ||||||
| chr10:22346653
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+835A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346653 | ||||||
| chr10:22346780
|
T | C | 1 | a0002c0002t0002g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121+962T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346780 | ||||||
| chr10:22346973
|
C | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+1155C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22346973 | ||||||
| chr10:22347141
|
T | C | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+1323T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22347141 | ||||||
| chr10:22347181
|
A | G | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.121+1363A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22347181 | ||||||
| chr10:22348002
|
C | CTTTCTTT others(4): Show |
48 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(45): Show | 49 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.121+2191_121+2192i others(13): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22348002 | |||||
| chr10:22348150
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.121+2332C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348150 | ||||||
| chr10:22348179
|
C | T | 1 | a0002c0002t0008g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.121+2361C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348179 | ||||||
| chr10:22348330
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0127 | 2 | HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.121+2512A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348330 | ||||||
| chr10:22348331
|
A | T | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+2513A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348331 | ||||||
| chr10:22348452
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+2634A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348452 | ||||||
| chr10:22348605
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.121+2787C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348605 | ||||||
| chr10:22348656
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121+2838G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348656 | ||||||
| chr10:22348761
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.121+2943A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348761 | ||||||
| chr10:22348851
|
G | A | 3 | a0002c0002t0001g0019a0002c0002t0001g0022a0002c0002t0001g0025 | 3 | HG02451.hp1 HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.121+3033G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348851 | ||||||
| chr10:22348883
|
A | G | 1 | a0002c0002t0003g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.121+3065A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348883 | ||||||
| chr10:22348895
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+3077C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348895 | ||||||
| chr10:22348897
|
A | G | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+3079A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348897 | ||||||
| chr10:22348975
|
G | A | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+3157G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22348975 | ||||||
| chr10:22349095
|
C | T | 1 | a0002c0002t0001g0134 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.121+3277C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349095 | ||||||
| chr10:22349190
|
G | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+3372G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349190 | ||||||
| chr10:22349219
|
GT | G | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+3412delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22349219 | |||||
| chr10:22349511
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0056 | 2 | HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.121+3693G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349511 | ||||||
| chr10:22349525
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.121+3707C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349525 | ||||||
| chr10:22349571
|
T | C | 1 | a0002c0002t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.121+3753T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349571 | ||||||
| chr10:22349672
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.121+3854A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22349672 | ||||||
| chr10:22350310
|
AT | A | 11 | a0002c0002t0001g0042a0002c0002t0001g0068a0002c0002t0002g0055others(8): Show | 11 | HG01975.hp2 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.121+4496delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22350310 | |||||
| chr10:22350377
|
G | C | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+4559G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22350377 | ||||||
| chr10:22350382
|
T | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+4564T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22350382 | ||||||
| chr10:22350473
|
A | G | 3 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016 | 3 | HG02723.hp1 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.121+4655A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22350473 | ||||||
| chr10:22350778
|
C | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+4960C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22350778 | ||||||
| chr10:22350820
|
TGCATA | T | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+5008_121+5012d others(7): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22350820 | |||||
| chr10:22350974
|
C | T | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+5156C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22350974 | ||||||
| chr10:22351022
|
G | A | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+5204G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22351022 | ||||||
| chr10:22351173
|
C | T | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121+5355C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22351173 | ||||||
| chr10:22351598
|
A | G | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121+5780A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22351598 | ||||||
| chr10:22351668
|
A | G | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+5850A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22351668 | ||||||
| chr10:22351889
|
G | A | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.121+6071G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22351889 | ||||||
| chr10:22352068
|
G | A | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+6250G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352068 | ||||||
| chr10:22352093
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.121+6275G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352093 | ||||||
| chr10:22352140
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+6322G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352140 | ||||||
| chr10:22352163
|
A | C | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+6345A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352163 | ||||||
| chr10:22352209
|
A | ATG | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0004g0086others(3): Show | 6 | HG00642.hp1 HG02258.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+6407_121+6408d others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22352209 | |||||
| chr10:22352339
|
A | G | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+6521A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352339 | ||||||
| chr10:22352386
|
A | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0088a0002c0002t0002g0055others(2): Show | 5 | HG00735.hp2 HG01975.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+6568A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352386 | ||||||
| chr10:22352408
|
A | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+6590A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352408 | ||||||
| chr10:22352493
|
T | C | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+6675T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352493 | ||||||
| chr10:22352698
|
A | G | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+6880A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352698 | ||||||
| chr10:22352724
|
G | T | 1 | a0002c0002t0006g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+6906G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352724 | ||||||
| chr10:22352842
|
A | T | 1 | a0001c0001t0001g0003 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.121+7024A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352842 | ||||||
| chr10:22352843
|
T | A | 1 | a0001c0001t0001g0003 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.121+7025T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352843 | ||||||
| chr10:22352907
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.121+7089C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352907 | ||||||
| chr10:22352985
|
C | T | 51 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(48): Show | 52 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.121+7167C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22352985 | ||||||
| chr10:22353239
|
T | C | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+7421T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22353239 | ||||||
| chr10:22353322
|
C | T | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+7504C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22353322 | ||||||
| chr10:22353435
|
A | C | 1 | a0002c0002t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.121+7617A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22353435 | ||||||
| chr10:22353843
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0084others(1): Show | 4 | HG01515.hp2 HG01934.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+8025C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22353843 | ||||||
| chr10:22353963
|
T | C | 1 | a0002c0002t0008g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.121+8145T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22353963 | ||||||
| chr10:22354075
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.121+8257C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354075 | ||||||
| chr10:22354230
|
A | T | 18 | a0002c0002t0001g0042a0002c0002t0002g0004a0002c0002t0002g0013others(15): Show | 19 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.121+8412A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354230 | ||||||
| chr10:22354429
|
T | C | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8611T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354429 | ||||||
| chr10:22354788
|
A | T | 51 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(48): Show | 52 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.121+8970A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354788 | ||||||
| chr10:22354823
|
A | T | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+9005A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354823 | ||||||
| chr10:22354834
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+9016C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354834 | ||||||
| chr10:22354969
|
G | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+9151G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22354969 | ||||||
| chr10:22354993
|
C | CA | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+9190dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22354993 | |||||
| chr10:22355148
|
T | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+9330T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355148 | ||||||
| chr10:22355212
|
G | C | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121+9394G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355212 | ||||||
| chr10:22355461
|
T | A | 13 | a0002c0002t0002g0004a0002c0002t0002g0013a0002c0002t0002g0043others(10): Show | 14 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-9392T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355461 | ||||||
| chr10:22355486
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-9367T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355486 | ||||||
| chr10:22355564
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0056 | 2 | HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.122-9289A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355564 | ||||||
| chr10:22355909
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-8944T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22355909 | ||||||
| chr10:22356057
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 118 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.122-8796T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356057 | ||||||
| chr10:22356134
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.122-8719A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356134 | ||||||
| chr10:22356339
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.122-8514A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356339 | ||||||
| chr10:22356361
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.122-8492G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356361 | ||||||
| chr10:22356486
|
A | C | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122-8367A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356486 | ||||||
| chr10:22356766
|
A | G | 1 | a0002c0002t0003g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122-8087A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356766 | ||||||
| chr10:22356783
|
G | A | 3 | a0002c0002t0001g0020a0002c0002t0001g0023a0002c0002t0009g0017 | 3 | HG02486.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122-8070G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356783 | ||||||
| chr10:22356869
|
C | A | 4 | a0002c0002t0002g0013a0002c0002t0002g0087a0002c0002t0002g0116others(1): Show | 4 | HG02572.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-7984C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22356869 | ||||||
| chr10:22357234
|
C | G | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.122-7619C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357234 | ||||||
| chr10:22357442
|
A | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-7411A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357442 | ||||||
| chr10:22357613
|
T | C | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-7240T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357613 | ||||||
| chr10:22357834
|
G | A | 4 | a0002c0002t0002g0013a0002c0002t0002g0087a0002c0002t0002g0116others(1): Show | 4 | HG02572.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-7019G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357834 | ||||||
| chr10:22357908
|
C | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6945C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357908 | ||||||
| chr10:22357912
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6941G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357912 | ||||||
| chr10:22357969
|
T | G | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-6884T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22357969 | ||||||
| chr10:22358007
|
C | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6846C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358007 | ||||||
| chr10:22358034
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6819G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358034 | ||||||
| chr10:22358117
|
G | T | 3 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016 | 3 | HG02723.hp1 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.122-6736G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358117 | ||||||
| chr10:22358176
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6677G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358176 | ||||||
| chr10:22358318
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6535C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358318 | ||||||
| chr10:22358330
|
G | A | 9 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-6523G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358330 | ||||||
| chr10:22358367
|
G | A | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.122-6486G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358367 | ||||||
| chr10:22358412
|
G | A | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-6441G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358412 | ||||||
| chr10:22358722
|
G | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.122-6131G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358722 | ||||||
| chr10:22358832
|
G | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-6021G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358832 | ||||||
| chr10:22358884
|
A | G | 1 | a0002c0002t0003g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.122-5969A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22358884 | ||||||
| chr10:22359151
|
C | G | 27 | a0002c0002t0001g0042a0002c0002t0001g0068a0002c0002t0002g0004others(24): Show | 28 | HG01071.hp1 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-5702C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359151 | ||||||
| chr10:22359266
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-5587T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359266 | ||||||
| chr10:22359276
|
A | C | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.122-5577A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359276 | ||||||
| chr10:22359435
|
C | A | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-5418C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359435 | ||||||
| chr10:22359524
|
G | C | 1 | a0002c0002t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122-5329G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359524 | ||||||
| chr10:22359613
|
G | C | 1 | a0002c0002t0002g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-5240G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22359613 | ||||||
| chr10:22360290
|
A | T | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-4563A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22360290 | ||||||
| chr10:22360465
|
C | CA | 6 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-4372dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22360465 | |||||
| chr10:22360888
|
T | TTTCC | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3944_122-3941d others(6): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22360888 | |||||
| chr10:22361344
|
G | C | 1 | a0002c0002t0002g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122-3509G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22361344 | ||||||
| chr10:22361442
|
T | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-3411T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22361442 | ||||||
| chr10:22361600
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.122-3253G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22361600 | ||||||
| chr10:22361611
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.122-3242A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22361611 | ||||||
| chr10:22361814
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.122-3039A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22361814 | ||||||
| chr10:22362060
|
T | C | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-2793T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362060 | ||||||
| chr10:22362067
|
G | A | 64 | a0001c0001t0001g0089a0001c0001t0005g0005a0001c0001t0005g0006others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.122-2786G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362067 | ||||||
| chr10:22362399
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122-2454T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362399 | ||||||
| chr10:22362586
|
T | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-2267T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362586 | ||||||
| chr10:22362819
|
A | T | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.122-2034A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362819 | ||||||
| chr10:22362864
|
A | C | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1989A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362864 | ||||||
| chr10:22362884
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.122-1969G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22362884 | ||||||
| chr10:22363099
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.122-1754G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22363099 | ||||||
| chr10:22363216
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.122-1637A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22363216 | ||||||
| chr10:22363288
|
A | G | 16 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(13): Show | 16 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-1565A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22363288 | ||||||
| chr10:22363845
|
A | T | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.122-1008A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22363845 | ||||||
| chr10:22364162
|
CAATT | C | 17 | a0002c0002t0002g0004a0002c0002t0002g0013a0002c0002t0002g0043others(14): Show | 18 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-688_122-685del others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22364162 | |||||
| chr10:22364358
|
A | T | 3 | a0002c0002t0001g0020a0002c0002t0001g0023a0002c0002t0009g0017 | 3 | HG02486.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122-495A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22364358 | ||||||
| chr10:22364573
|
C | T | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-280C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | chr10 | 22364573 | ||||||
| chr10:22364752
|
A | AT | 2 | a0002c0002t0002g0004a0002c0002t0002g0109 | 3 | HG01175.hp2 HG01255.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.122-95dupT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | 22364752 | |||||
| chr10:22365501
|
C | T | 52 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0003t0001g0137others(49): Show | 53 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.288+482C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365501 | ||||||
| chr10:22365516
|
A | G | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.288+497A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365516 | ||||||
| chr10:22365527
|
T | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.288+508T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365527 | ||||||
| chr10:22365643
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.288+624T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365643 | ||||||
| chr10:22365708
|
C | G | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.288+689C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365708 | ||||||
| chr10:22365746
|
C | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.288+727C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22365746 | ||||||
| chr10:22366087
|
A | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+1068A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366087 | ||||||
| chr10:22366151
|
G | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0047a0001c0001t0001g0094others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+1132G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366151 | ||||||
| chr10:22366280
|
A | G | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.288+1261A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366280 | ||||||
| chr10:22366480
|
A | G | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.288+1461A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366480 | ||||||
| chr10:22366496
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.288+1477T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366496 | ||||||
| chr10:22366668
|
A | C | 1 | a0002c0002t0001g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.288+1649A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366668 | ||||||
| chr10:22366876
|
A | C | 1 | a0002c0002t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.289-1619A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366876 | ||||||
| chr10:22366900
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.289-1595G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22366900 | ||||||
| chr10:22367008
|
G | GT | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-1487_289-1486i others(3): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367008 | ||||||
| chr10:22367009
|
G | T | 23 | a0001c0001t0005g0005a0002c0002t0001g0008a0002c0002t0001g0009others(20): Show | 23 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.289-1486G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367009 | ||||||
| chr10:22367034
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.289-1461A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367034 | ||||||
| chr10:22367550
|
T | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.289-945T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367550 | ||||||
| chr10:22367853
|
TA | T | 20 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(17): Show | 20 | HG00642.hp1 HG02109.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.289-633delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 22367853 | |||||
| chr10:22367885
|
A | T | 17 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(14): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-610A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367885 | ||||||
| chr10:22367914
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.289-581C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22367914 | ||||||
| chr10:22368187
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0088others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.289-308T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 3/10 | chr10 | 22368187 | ||||||
| chr10:22368849
|
CA | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0121a0002c0002t0002g0004others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+180delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22368849 | |||||
| chr10:22368858
|
A | AC | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+183dupC | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22368858 | |||||
| chr10:22368858
|
A | C | 22 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(19): Show | 22 | HG00642.hp1 HG02109.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.472+180A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22368858 | ||||||
| chr10:22369043
|
A | G | 1 | a0002c0002t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.472+365A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369043 | ||||||
| chr10:22369090
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.472+412G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369090 | ||||||
| chr10:22369102
|
C | T | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.472+424C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369102 | ||||||
| chr10:22369181
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+503C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369181 | ||||||
| chr10:22369352
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(113): Show | 118 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.472+674G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369352 | ||||||
| chr10:22369468
|
A | G | 1 | a0002c0002t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.472+790A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22369468 | ||||||
| chr10:22370010
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.472+1332C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22370010 | ||||||
| chr10:22371014
|
T | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+2336T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371014 | ||||||
| chr10:22371093
|
A | C | 13 | a0001c0001t0001g0089a0001c0001t0005g0123a0002c0002t0003g0111others(10): Show | 13 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.472+2415A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371093 | ||||||
| chr10:22371440
|
G | T | 2 | a0002c0002t0001g0042a0002c0002t0002g0102 | 2 | HG01975.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+2762G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371440 | ||||||
| chr10:22371466
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.472+2788C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371466 | ||||||
| chr10:22371562
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+2884G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371562 | ||||||
| chr10:22371783
|
C | T | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+3105C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371783 | ||||||
| chr10:22371886
|
G | A | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.472+3208G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22371886 | ||||||
| chr10:22372192
|
A | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0033others(9): Show | 13 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.472+3514A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372192 | ||||||
| chr10:22372316
|
A | T | 1 | a0002c0002t0003g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.472+3638A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372316 | ||||||
| chr10:22372413
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.472+3735C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372413 | ||||||
| chr10:22372572
|
A | C | 1 | a0002c0002t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.472+3894A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372572 | ||||||
| chr10:22372658
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.472+3980G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372658 | ||||||
| chr10:22372762
|
T | TA | 5 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0042others(2): Show | 5 | HG00642.hp1 HG02602.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+4100dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22372762 | |||||
| chr10:22372762
|
TA | T | 5 | a0001c0001t0001g0046a0002c0002t0002g0108a0002c0002t0006g0053others(2): Show | 5 | HG01243.hp1 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+4100delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22372762 | |||||
| chr10:22372778
|
AG | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.472+4101delG | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372778 | ||||||
| chr10:22372779
|
G | A | 19 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(16): Show | 19 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.472+4101G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372779 | ||||||
| chr10:22372838
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.472+4160T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372838 | ||||||
| chr10:22372974
|
A | G | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.472+4296A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22372974 | ||||||
| chr10:22373030
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472+4352T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373030 | ||||||
| chr10:22373471
|
A | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+4793A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373471 | ||||||
| chr10:22373483
|
C | G | 16 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(13): Show | 16 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+4805C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373483 | ||||||
| chr10:22373536
|
A | G | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.472+4858A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373536 | ||||||
| chr10:22373615
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472+4937C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373615 | ||||||
| chr10:22373622
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472+4944C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373622 | ||||||
| chr10:22373673
|
C | T | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.472+4995C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373673 | ||||||
| chr10:22373868
|
G | A | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.472+5190G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373868 | ||||||
| chr10:22373883
|
A | G | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+5205A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22373883 | ||||||
| chr10:22374018
|
C | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.472+5340C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374018 | ||||||
| chr10:22374266
|
A | T | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+5588A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374266 | ||||||
| chr10:22374331
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.472+5653G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374331 | ||||||
| chr10:22374372
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0073 | 2 | HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.472+5694C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374372 | ||||||
| chr10:22374547
|
C | G | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.472+5869C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374547 | ||||||
| chr10:22374602
|
T | TA | 8 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0075others(5): Show | 8 | HG01175.hp2 HG01192.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+5948dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22374602 | |||||
| chr10:22374602
|
T | TAA | 15 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(12): Show | 15 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+5947_472+5948d others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22374602 | |||||
| chr10:22374602
|
T | TAAA | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(6): Show | 9 | HG00642.hp1 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.472+5946_472+5948d others(5): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22374602 | |||||
| chr10:22374879
|
C | T | 5 | a0002c0002t0001g0042a0002c0002t0002g0055a0002c0002t0002g0069others(2): Show | 5 | HG01975.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+6201C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374879 | ||||||
| chr10:22374890
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.472+6212G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22374890 | ||||||
| chr10:22374957
|
T | TA | 2 | a0001c0001t0001g0036a0001c0001t0001g0073 | 2 | HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.472+6280dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22374957 | |||||
| chr10:22375079
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0033others(2): Show | 6 | HG02109.hp1 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+6401A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375079 | ||||||
| chr10:22375212
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0095 | 2 | HG03927.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.472+6534T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375212 | ||||||
| chr10:22375674
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.472+6996G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375674 | ||||||
| chr10:22375682
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.472+7004G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375682 | ||||||
| chr10:22375697
|
G | T | 1 | a0002c0002t0001g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.472+7019G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375697 | ||||||
| chr10:22375698
|
A | C | 27 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(24): Show | 27 | HG00642.hp1 HG01243.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.472+7020A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375698 | ||||||
| chr10:22375779
|
G | A | 1 | a0002c0002t0006g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.472+7101G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375779 | ||||||
| chr10:22375990
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.472+7312G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22375990 | ||||||
| chr10:22376128
|
A | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+7450A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376128 | ||||||
| chr10:22376234
|
G | A | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.472+7556G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376234 | ||||||
| chr10:22376240
|
T | A | 1 | a0001c0001t0005g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.472+7562T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376240 | ||||||
| chr10:22376364
|
T | C | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.472+7686T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376364 | ||||||
| chr10:22376423
|
T | G | 3 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0125 | 3 | HG03486.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.472+7745T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376423 | ||||||
| chr10:22376528
|
A | T | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.472+7850A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376528 | ||||||
| chr10:22376634
|
C | CGT | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+7956_472+7957i others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376634 | ||||||
| chr10:22376635
|
A | ATG | 2 | a0002c0002t0002g0055a0002c0002t0002g0069 | 2 | HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.472+7975_472+7976d others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22376635 | |||||
| chr10:22376635
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+7957A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22376635 | ||||||
| chr10:22377182
|
G | A | 24 | a0002c0002t0001g0042a0002c0002t0001g0068a0002c0002t0002g0004others(21): Show | 25 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.472+8504G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377182 | ||||||
| chr10:22377235
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.472+8557C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377235 | ||||||
| chr10:22377283
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.472+8605C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377283 | ||||||
| chr10:22377365
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.472+8687G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377365 | ||||||
| chr10:22377728
|
T | G | 66 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0005g0005others(63): Show | 67 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(64): Show |
intron_variant | MODIFIER | c.473-9026T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377728 | ||||||
| chr10:22377745
|
A | G | 21 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.473-9009A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377745 | ||||||
| chr10:22377870
|
A | T | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.473-8884A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22377870 | ||||||
| chr10:22378055
|
C | CT | 5 | a0001c0001t0001g0073a0001c0001t0001g0099a0002c0002t0006g0053others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-8679dupT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22378055 | |||||
| chr10:22378055
|
CT | C | 33 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(30): Show | 34 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.473-8679delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22378055 | |||||
| chr10:22378072
|
T | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-8682T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378072 | ||||||
| chr10:22378263
|
T | C | 23 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(20): Show | 23 | HG00642.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-8491T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378263 | ||||||
| chr10:22378417
|
GT | G | 10 | a0001c0001t0001g0089a0001c0001t0005g0005a0001c0001t0005g0006others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-8319delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22378417 | |||||
| chr10:22378565
|
T | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.473-8189T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378565 | ||||||
| chr10:22378630
|
G | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0001g0008others(21): Show | 24 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.473-8124G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378630 | ||||||
| chr10:22378661
|
A | G | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.473-8093A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378661 | ||||||
| chr10:22378938
|
A | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0105 | 2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.473-7816A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378938 | ||||||
| chr10:22378955
|
C | A | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.473-7799C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22378955 | ||||||
| chr10:22379154
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.473-7600C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22379154 | ||||||
| chr10:22379391
|
C | T | 3 | a0002c0002t0001g0068a0002c0002t0002g0110a0002c0002t0002g0122 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.473-7363C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22379391 | ||||||
| chr10:22379951
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.473-6803T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22379951 | ||||||
| chr10:22380263
|
A | G | 17 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(14): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.473-6491A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380263 | ||||||
| chr10:22380293
|
TTTTG | T | 7 | a0001c0001t0001g0089a0002c0002t0003g0113a0002c0002t0003g0114others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.473-6437_473-6434d others(6): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22380293 | |||||
| chr10:22380358
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0002c0002t0008g0007 | 3 | HG00642.hp1 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.473-6396A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380358 | ||||||
| chr10:22380417
|
C | A | 17 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(14): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.473-6337C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380417 | ||||||
| chr10:22380507
|
C | T | 17 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(14): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.473-6247C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380507 | ||||||
| chr10:22380751
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.473-6003C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380751 | ||||||
| chr10:22380800
|
A | C | 1 | a0002c0002t0002g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.473-5954A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22380800 | ||||||
| chr10:22381140
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.473-5614C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22381140 | ||||||
| chr10:22381318
|
TCA | T | 11 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(8): Show | 11 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.473-5431_473-5430d others(4): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22381318 | |||||
| chr10:22381576
|
G | T | 1 | a0002c0002t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.473-5178G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22381576 | ||||||
| chr10:22382048
|
A | G | 1 | a0002c0002t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.473-4706A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382048 | ||||||
| chr10:22382187
|
T | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(114): Show | 119 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.473-4567T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382187 | ||||||
| chr10:22382236
|
T | C | 5 | a0001c0003t0001g0137a0002c0002t0001g0134a0002c0002t0001g0135others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-4518T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382236 | ||||||
| chr10:22382355
|
G | A | 60 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(57): Show | 61 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.473-4399G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382355 | ||||||
| chr10:22382579
|
C | T | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.473-4175C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382579 | ||||||
| chr10:22382586
|
A | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.473-4168A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382586 | ||||||
| chr10:22382616
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0105 | 2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.473-4138A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382616 | ||||||
| chr10:22382754
|
C | T | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.473-4000C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382754 | ||||||
| chr10:22382889
|
G | T | 59 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(56): Show | 60 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.473-3865G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22382889 | ||||||
| chr10:22383499
|
C | T | 4 | a0002c0002t0002g0013a0002c0002t0002g0087a0002c0002t0002g0116others(1): Show | 4 | HG02572.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-3255C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22383499 | ||||||
| chr10:22383531
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.473-3223C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22383531 | ||||||
| chr10:22383726
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.473-3028T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22383726 | ||||||
| chr10:22383763
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0093 | 3 | HG02922.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.473-2991C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22383763 | ||||||
| chr10:22384091
|
C | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.473-2663C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384091 | ||||||
| chr10:22384204
|
C | T | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-2550C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384204 | ||||||
| chr10:22384383
|
A | G | 1 | a0002c0002t0008g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.473-2371A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384383 | ||||||
| chr10:22384537
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.473-2217A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384537 | ||||||
| chr10:22384748
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.473-2006T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384748 | ||||||
| chr10:22384770
|
C | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.473-1984C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384770 | ||||||
| chr10:22384773
|
C | T | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-1981C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384773 | ||||||
| chr10:22384890
|
G | A | 56 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(53): Show | 57 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.473-1864G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384890 | ||||||
| chr10:22384947
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0056 | 2 | HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.473-1807C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384947 | ||||||
| chr10:22384956
|
T | G | 5 | a0001c0003t0001g0137a0002c0002t0001g0134a0002c0002t0001g0135others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-1798T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384956 | ||||||
| chr10:22384995
|
G | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.473-1759G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22384995 | ||||||
| chr10:22385146
|
G | A | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.473-1608G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22385146 | ||||||
| chr10:22385507
|
G | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.473-1247G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22385507 | ||||||
| chr10:22385528
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG00642.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.473-1226T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22385528 | ||||||
| chr10:22385904
|
G | A | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.473-850G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22385904 | ||||||
| chr10:22385989
|
C | T | 37 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(34): Show | 38 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.473-765C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22385989 | ||||||
| chr10:22386140
|
T | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.473-614T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386140 | ||||||
| chr10:22386189
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0039 | 3 | HG01255.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.473-565G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386189 | ||||||
| chr10:22386204
|
T | G | 5 | a0001c0003t0001g0137a0002c0002t0001g0134a0002c0002t0001g0135others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-550T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386204 | ||||||
| chr10:22386241
|
T | G | 1 | a0002c0002t0002g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.473-513T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386241 | ||||||
| chr10:22386356
|
T | G | 1 | a0002c0002t0002g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.473-398T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386356 | ||||||
| chr10:22386437
|
T | G | 17 | a0002c0002t0002g0004a0002c0002t0002g0013a0002c0002t0002g0043others(14): Show | 18 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.473-317T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | chr10 | 22386437 | ||||||
| chr10:22386482
|
T | TA | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(3): Show | 6 | HG00642.hp1 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-258dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22386482 | |||||
| chr10:22386482
|
TA | T | 20 | a0001c0001t0007g0038a0001c0001t0007g0066a0002c0002t0001g0014others(17): Show | 21 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.473-258delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr10 | 22386482 | |||||
| chr10:22387159
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.678+200A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 5/10 | chr10 | 22387159 | ||||||
| chr10:22387310
|
G | A | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.678+351G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 5/10 | chr10 | 22387310 | ||||||
| chr10:22387386
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.678+427T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 5/10 | chr10 | 22387386 | ||||||
| chr10:22387428
|
A | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-395A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 5/10 | chr10 | 22387428 | ||||||
| chr10:22388186
|
C | T | 49 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(46): Show | 50 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.852+190C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 6/10 | chr10 | 22388186 | ||||||
| chr10:22388300
|
C | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.852+304C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 6/10 | chr10 | 22388300 | ||||||
| chr10:22388551
|
T | C | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.852+555T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 6/10 | chr10 | 22388551 | ||||||
| chr10:22388808
|
A | T | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853-352A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 6/10 | chr10 | 22388808 | ||||||
| chr10:22389414
|
C | CA | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+109dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr10 | 22389414 | |||||
| chr10:22389431
|
A | T | 1 | a0002c0002t0001g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1005+119A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22389431 | ||||||
| chr10:22389507
|
G | A | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+195G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22389507 | ||||||
| chr10:22389521
|
G | C | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+209G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22389521 | ||||||
| chr10:22389837
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1005+525C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22389837 | ||||||
| chr10:22389963
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0096 | 2 | HG00621.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1005+651G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22389963 | ||||||
| chr10:22390009
|
G | T | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1005+697G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390009 | ||||||
| chr10:22390069
|
AT | A | 5 | a0002c0002t0002g0004a0002c0002t0002g0043a0002c0002t0002g0044others(2): Show | 6 | HG01175.hp2 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+765delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr10 | 22390069 | |||||
| chr10:22390172
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0059 | 2 | NA18957.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1005+860T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390172 | ||||||
| chr10:22390248
|
G | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+936G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390248 | ||||||
| chr10:22390297
|
A | G | 2 | a0002c0002t0003g0131a0002c0002t0003g0132 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1005+985A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390297 | ||||||
| chr10:22390355
|
A | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+1043A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390355 | ||||||
| chr10:22390502
|
A | G | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1005+1190A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390502 | ||||||
| chr10:22390640
|
A | G | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006-1089A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390640 | ||||||
| chr10:22390770
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1006-959C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390770 | ||||||
| chr10:22390867
|
A | T | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1006-862A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390867 | ||||||
| chr10:22390981
|
C | T | 1 | a0002c0002t0003g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1006-748C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22390981 | ||||||
| chr10:22391196
|
A | G | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1006-533A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391196 | ||||||
| chr10:22391255
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1006-474G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391255 | ||||||
| chr10:22391346
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0089 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1006-383T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391346 | ||||||
| chr10:22391410
|
A | T | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006-319A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391410 | ||||||
| chr10:22391424
|
C | G | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-305C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391424 | ||||||
| chr10:22391433
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1006-296C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391433 | ||||||
| chr10:22391479
|
T | C | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1006-250T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 7/10 | chr10 | 22391479 | ||||||
| chr10:22391993
|
T | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1197+73T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22391993 | ||||||
| chr10:22392511
|
T | C | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+591T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22392511 | ||||||
| chr10:22393182
|
C | A | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1197+1262C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22393182 | ||||||
| chr10:22393347
|
A | G | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1197+1427A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22393347 | ||||||
| chr10:22393859
|
A | G | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1197+1939A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22393859 | ||||||
| chr10:22393939
|
T | C | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+2019T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22393939 | ||||||
| chr10:22394293
|
GT | G | 23 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(20): Show | 24 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1197+2375delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr10 | 22394293 | |||||
| chr10:22394324
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1197+2404A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22394324 | ||||||
| chr10:22394422
|
G | T | 20 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(17): Show | 21 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1197+2502G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22394422 | ||||||
| chr10:22394481
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1197+2561A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22394481 | ||||||
| chr10:22394508
|
T | C | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1197+2588T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22394508 | ||||||
| chr10:22395190
|
A | C | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+3270A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22395190 | ||||||
| chr10:22395306
|
T | C | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1197+3386T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22395306 | ||||||
| chr10:22395322
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1197+3402A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22395322 | ||||||
| chr10:22395498
|
CA | C | 6 | a0002c0002t0003g0113a0002c0002t0003g0114a0002c0002t0003g0128others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+3579delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22395498 | ||||||
| chr10:22395643
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1197+3723A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22395643 | ||||||
| chr10:22396051
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1197+4131A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396051 | ||||||
| chr10:22396093
|
G | T | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+4173G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396093 | ||||||
| chr10:22396119
|
G | C | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+4199G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396119 | ||||||
| chr10:22396273
|
T | G | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1197+4353T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396273 | ||||||
| chr10:22396291
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1197+4371G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396291 | ||||||
| chr10:22396707
|
TA | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1198-4446delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr10 | 22396707 | |||||
| chr10:22396817
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1198-4344T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396817 | ||||||
| chr10:22396843
|
G | A | 1 | a0002c0002t0003g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1198-4318G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22396843 | ||||||
| chr10:22397217
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1198-3944C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22397217 | ||||||
| chr10:22397276
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG01175.hp1 HG02004.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198-3885A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22397276 | ||||||
| chr10:22397339
|
A | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198-3822A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22397339 | ||||||
| chr10:22397592
|
G | C | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1198-3569G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22397592 | ||||||
| chr10:22398209
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1198-2952A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22398209 | ||||||
| chr10:22398219
|
T | C | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1198-2942T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22398219 | ||||||
| chr10:22398407
|
TA | T | 38 | a0001c0001t0001g0058a0002c0002t0001g0068a0002c0002t0002g0004others(35): Show | 39 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.1198-2745delA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr10 | 22398407 | |||||
| chr10:22398828
|
T | A | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1198-2333T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22398828 | ||||||
| chr10:22399018
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1198-2143C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399018 | ||||||
| chr10:22399052
|
C | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0138 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1198-2109C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399052 | ||||||
| chr10:22399251
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1198-1910G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399251 | ||||||
| chr10:22399480
|
T | C | 12 | a0002c0002t0001g0021a0002c0002t0003g0111a0002c0002t0003g0112others(9): Show | 12 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-1681T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399480 | ||||||
| chr10:22399685
|
T | C | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1198-1476T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399685 | ||||||
| chr10:22399761
|
A | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1198-1400A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22399761 | ||||||
| chr10:22400127
|
A | C | 49 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(46): Show | 50 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.1198-1034A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22400127 | ||||||
| chr10:22400240
|
A | T | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1198-921A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22400240 | ||||||
| chr10:22400475
|
A | G | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198-686A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22400475 | ||||||
| chr10:22400536
|
C | A | 1 | a0002c0002t0003g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1198-625C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22400536 | ||||||
| chr10:22400762
|
A | G | 1 | a0002c0002t0003g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1198-399A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22400762 | ||||||
| chr10:22401018
|
A | G | 3 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016 | 3 | HG02723.hp1 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1198-143A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22401018 | ||||||
| chr10:22401089
|
T | G | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1198-72T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 8/10 | chr10 | 22401089 | ||||||
| chr10:22401560
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG00642.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1314+283T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401560 | ||||||
| chr10:22401627
|
G | A | 2 | a0002c0002t0003g0131a0002c0002t0003g0132 | 2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1314+350G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401627 | ||||||
| chr10:22401695
|
G | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+418G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401695 | ||||||
| chr10:22401707
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1314+430G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401707 | ||||||
| chr10:22401715
|
C | T | 1 | a0002c0002t0003g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1314+438C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401715 | ||||||
| chr10:22401726
|
G | A | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1314+449G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401726 | ||||||
| chr10:22401855
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1314+578A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22401855 | ||||||
| chr10:22402009
|
G | A | 37 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(34): Show | 38 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1314+732G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402009 | ||||||
| chr10:22402057
|
C | T | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1314+780C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402057 | ||||||
| chr10:22402121
|
G | A | 49 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(46): Show | 50 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.1314+844G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402121 | ||||||
| chr10:22402367
|
C | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+1090C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402367 | ||||||
| chr10:22402483
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1314+1206G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402483 | ||||||
| chr10:22402570
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1314+1293A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22402570 | ||||||
| chr10:22403253
|
G | T | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1314+1976G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403253 | ||||||
| chr10:22403283
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1314+2006C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403283 | ||||||
| chr10:22403283
|
C | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+2006C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403283 | ||||||
| chr10:22403380
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1314+2103C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403380 | ||||||
| chr10:22403577
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1314+2300T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403577 | ||||||
| chr10:22403579
|
G | A | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1314+2302G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403579 | ||||||
| chr10:22403583
|
C | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1314+2306C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403583 | ||||||
| chr10:22403584
|
A | G | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1314+2307A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403584 | ||||||
| chr10:22403605
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0088 | 2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1314+2328G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403605 | ||||||
| chr10:22403949
|
C | G | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1314+2672C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403949 | ||||||
| chr10:22403961
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1314+2684C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22403961 | ||||||
| chr10:22404310
|
G | A | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1314+3033G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404310 | ||||||
| chr10:22404454
|
G | A | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1314+3177G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404454 | ||||||
| chr10:22404457
|
G | A | 56 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(53): Show | 57 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.1314+3180G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404457 | ||||||
| chr10:22404567
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1314+3290C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404567 | ||||||
| chr10:22404706
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0007g0038others(1): Show | 4 | HG02155.hp2 NA18957.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+3429A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404706 | ||||||
| chr10:22404744
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1314+3467A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404744 | ||||||
| chr10:22404755
|
T | G | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1314+3478T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404755 | ||||||
| chr10:22404892
|
C | G | 1 | a0002c0002t0001g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1314+3615C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22404892 | ||||||
| chr10:22404947
|
T | TGGTGTAT others(1): Show |
3 | a0002c0002t0002g0013a0002c0002t0002g0116a0002c0002t0002g0124 | 3 | HG02572.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1314+3671_1314+367 others(12): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | 22404947 | |||||
| chr10:22405036
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1314+3759G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405036 | ||||||
| chr10:22405178
|
A | C | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+3901A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405178 | ||||||
| chr10:22405191
|
G | A | 2 | a0002c0002t0002g0110a0002c0002t0002g0122 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1314+3914G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405191 | ||||||
| chr10:22405198
|
C | A | 14 | a0002c0002t0002g0004a0002c0002t0002g0013a0002c0002t0002g0043others(11): Show | 15 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1314+3921C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405198 | ||||||
| chr10:22405198
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1314+3921C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405198 | ||||||
| chr10:22405503
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1314+4226G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405503 | ||||||
| chr10:22405561
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1314+4284G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405561 | ||||||
| chr10:22405580
|
A | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+4303A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405580 | ||||||
| chr10:22405719
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1314+4442C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405719 | ||||||
| chr10:22405732
|
G | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1314+4455G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22405732 | ||||||
| chr10:22406007
|
G | A | 1 | a0002c0002t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1314+4730G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406007 | ||||||
| chr10:22406349
|
G | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1315-4682G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406349 | ||||||
| chr10:22406402
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1315-4629A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406402 | ||||||
| chr10:22406558
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1315-4473G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406558 | ||||||
| chr10:22406586
|
G | A | 12 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1315-4445G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406586 | ||||||
| chr10:22406681
|
C | T | 1 | a0002c0002t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1315-4350C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406681 | ||||||
| chr10:22406864
|
T | C | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315-4167T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406864 | ||||||
| chr10:22406926
|
T | G | 3 | a0002c0002t0002g0055a0002c0002t0002g0069a0002c0002t0002g0108 | 3 | HG02896.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1315-4105T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22406926 | ||||||
| chr10:22407073
|
T | C | 1 | a0002c0002t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1315-3958T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407073 | ||||||
| chr10:22407118
|
A | G | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1315-3913A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407118 | ||||||
| chr10:22407218
|
G | T | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1315-3813G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407218 | ||||||
| chr10:22407277
|
G | A | 1 | a0002c0002t0006g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1315-3754G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407277 | ||||||
| chr10:22407299
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0062others(8): Show | 12 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1315-3732C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407299 | ||||||
| chr10:22407305
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1315-3726C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407305 | ||||||
| chr10:22407314
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1315-3717C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407314 | ||||||
| chr10:22407372
|
T | G | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315-3659T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407372 | ||||||
| chr10:22407484
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0067 | 2 | HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1315-3547A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407484 | ||||||
| chr10:22407497
|
C | T | 3 | a0002c0002t0004g0086a0002c0002t0004g0115a0002c0002t0004g0126 | 3 | HG02258.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1315-3534C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407497 | ||||||
| chr10:22407498
|
G | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1315-3533G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407498 | ||||||
| chr10:22407534
|
T | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0138 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1315-3497T>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407534 | ||||||
| chr10:22407632
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315-3399C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407632 | ||||||
| chr10:22407757
|
C | T | 1 | a0002c0002t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315-3274C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407757 | ||||||
| chr10:22407758
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0062others(8): Show | 12 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1315-3273G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407758 | ||||||
| chr10:22407859
|
C | A | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1315-3172C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407859 | ||||||
| chr10:22407925
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1315-3106C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407925 | ||||||
| chr10:22407930
|
T | C | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1315-3101T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407930 | ||||||
| chr10:22407957
|
C | T | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-3074C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22407957 | ||||||
| chr10:22408011
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1315-3020G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408011 | ||||||
| chr10:22408125
|
T | G | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1315-2906T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408125 | ||||||
| chr10:22408185
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1315-2846C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408185 | ||||||
| chr10:22408346
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1315-2685C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408346 | ||||||
| chr10:22408421
|
G | C | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1315-2610G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408421 | ||||||
| chr10:22408421
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0056 | 2 | HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1315-2610G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408421 | ||||||
| chr10:22408459
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1315-2572G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408459 | ||||||
| chr10:22408728
|
C | T | 11 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0113others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315-2303C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408728 | ||||||
| chr10:22408749
|
T | C | 4 | a0002c0002t0002g0013a0002c0002t0002g0087a0002c0002t0002g0116others(1): Show | 4 | HG02572.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-2282T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408749 | ||||||
| chr10:22408784
|
C | G | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1315-2247C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408784 | ||||||
| chr10:22408865
|
A | G | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1315-2166A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408865 | ||||||
| chr10:22408877
|
T | C | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1315-2154T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408877 | ||||||
| chr10:22408905
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1315-2126G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408905 | ||||||
| chr10:22408908
|
G | A | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1315-2123G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408908 | ||||||
| chr10:22408945
|
C | A | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-2086C>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408945 | ||||||
| chr10:22408991
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0119 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1315-2040C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408991 | ||||||
| chr10:22408997
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1315-2034G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22408997 | ||||||
| chr10:22409014
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1315-2017C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409014 | ||||||
| chr10:22409090
|
A | G | 64 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(61): Show | 65 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1315-1941A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409090 | ||||||
| chr10:22409121
|
T | C | 3 | a0002c0002t0002g0055a0002c0002t0002g0069a0002c0002t0002g0108 | 3 | HG02896.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1315-1910T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409121 | ||||||
| chr10:22409211
|
G | A | 53 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(50): Show | 54 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.1315-1820G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409211 | ||||||
| chr10:22409559
|
A | G | 1 | a0001c0003t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1315-1472A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409559 | ||||||
| chr10:22409592
|
A | G | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1315-1439A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409592 | ||||||
| chr10:22409689
|
C | T | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315-1342C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22409689 | ||||||
| chr10:22410220
|
CATTT | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1315-810_1315-807d others(6): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22410220 | ||||||
| chr10:22410231
|
C | T | 3 | a0002c0002t0006g0053a0002c0002t0006g0100a0002c0002t0006g0107 | 3 | HG01243.hp1 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1315-800C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22410231 | ||||||
| chr10:22410582
|
AG | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-448delG | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 9/10 | chr10 | 22410582 | ||||||
| chr10:22411234
|
A | C | 3 | a0002c0002t0003g0113a0002c0002t0003g0128a0002c0002t0003g0133 | 3 | HG02258.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1460+58A>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411234 | ||||||
| chr10:22411236
|
C | G | 1 | a0002c0002t0002g0102 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1460+60C>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411236 | ||||||
| chr10:22411254
|
G | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1460+78G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411254 | ||||||
| chr10:22411331
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1460+155C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411331 | ||||||
| chr10:22411530
|
C | T | 1 | a0002c0002t0008g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1460+354C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411530 | ||||||
| chr10:22411602
|
A | G | 1 | a0002c0002t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1460+426A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411602 | ||||||
| chr10:22411756
|
G | A | 1 | a0002c0002t0002g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1460+580G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411756 | ||||||
| chr10:22411840
|
C | CTTTTTTT | 6 | a0001c0001t0005g0006a0002c0002t0001g0008a0002c0002t0001g0010others(3): Show | 6 | HG00642.hp1 HG02257.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+684_1460+690d others(9): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1460+681_1460+690d others(12): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
C | CTTTTTTT others(4): Show |
6 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0020others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+680_1460+690d others(13): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
C | CTTTTTTT others(5): Show |
4 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0022others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+679_1460+690d others(14): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
C | CTTTTTTT others(10): Show |
1 | a0002c0002t0001g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1460+674_1460+690d others(19): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
CT | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(39): Show | 43 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1460+690delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411840
|
CTTTTT | C | 33 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(30): Show | 34 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.1460+686_1460+690d others(7): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22411840 | |||||
| chr10:22411883
|
C | T | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+707C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411883 | ||||||
| chr10:22411909
|
C | T | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1460+733C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411909 | ||||||
| chr10:22411984
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1460+808T>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22411984 | ||||||
| chr10:22412129
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1460+953G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412129 | ||||||
| chr10:22412148
|
C | T | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+972C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412148 | ||||||
| chr10:22412222
|
T | C | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1460+1046T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412222 | ||||||
| chr10:22412615
|
G | A | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1460+1439G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412615 | ||||||
| chr10:22412633
|
C | T | 1 | a0001c0001t0005g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1460+1457C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412633 | ||||||
| chr10:22412664
|
C | T | 1 | a0002c0002t0008g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1460+1488C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412664 | ||||||
| chr10:22412761
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0121 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1460+1585C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412761 | ||||||
| chr10:22412877
|
T | C | 7 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1460+1701T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412877 | ||||||
| chr10:22412918
|
G | A | 1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1460+1742G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22412918 | ||||||
| chr10:22413013
|
A | G | 1 | a0002c0002t0003g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1460+1837A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413013 | ||||||
| chr10:22413066
|
C | CA | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0036others(8): Show | 11 | HG00735.hp1 HG00735.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1460+1912dupA | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413066 | |||||
| chr10:22413066
|
C | CAAA | 11 | a0001c0001t0005g0123a0002c0002t0001g0008a0002c0002t0001g0009others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1460+1910_1460+191 others(7): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413066 | |||||
| chr10:22413066
|
C | CAAAA | 11 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0002g0087others(8): Show | 11 | HG01243.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1460+1909_1460+191 others(8): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413066 | |||||
| chr10:22413066
|
C | CAAAAA | 28 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(25): Show | 29 | HG01071.hp1 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1460+1908_1460+191 others(9): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413066 | |||||
| chr10:22413066
|
C | CAAAAAA | 10 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0025others(7): Show | 10 | HG01175.hp2 HG01975.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1460+1907_1460+191 others(10): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413066 | |||||
| chr10:22413159
|
GT | G | 51 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(48): Show | 52 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.1460+1996delT | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413159 | |||||
| chr10:22413224
|
G | C | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1460+2048G>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413224 | ||||||
| chr10:22413245
|
TAGTGCTG others(9): Show |
T | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1460+2074_1460+208 others(20): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413245 | |||||
| chr10:22413480
|
C | T | 60 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(57): Show | 61 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.1460+2304C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413480 | ||||||
| chr10:22413489
|
T | C | 3 | a0002c0002t0002g0055a0002c0002t0002g0069a0002c0002t0002g0108 | 3 | HG02896.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1460+2313T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413489 | ||||||
| chr10:22413528
|
G | A | 6 | a0002c0002t0002g0004a0002c0002t0002g0043a0002c0002t0002g0044others(3): Show | 7 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1460+2352G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413528 | ||||||
| chr10:22413687
|
T | TTATATAT others(7): Show |
6 | a0002c0002t0003g0113a0002c0002t0003g0114a0002c0002t0003g0128others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1460+2511_1460+251 others(18): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413687 | ||||||
| chr10:22413687
|
T | TTATATAT others(9): Show |
1 | a0002c0002t0003g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1460+2511_1460+251 others(20): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413687 | ||||||
| chr10:22413687
|
T | TTATATAT others(13): Show |
1 | a0002c0002t0003g0129 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1460+2511_1460+251 others(24): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413687 | ||||||
| chr10:22413688
|
G | GATATATA others(1): Show |
17 | a0002c0002t0002g0004a0002c0002t0002g0043a0002c0002t0002g0044others(14): Show | 18 | HG01071.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1460+2525_1460+253 others(12): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(3): Show |
9 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(6): Show | 9 | HG01975.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1460+2523_1460+253 others(14): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(5): Show |
8 | a0002c0002t0001g0014a0002c0002t0001g0022a0002c0002t0001g0025others(5): Show | 8 | HG02293.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+2521_1460+253 others(16): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(7): Show |
5 | a0002c0002t0001g0015a0002c0002t0001g0024a0002c0002t0004g0086others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1460+2519_1460+253 others(18): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(17): Show |
1 | a0002c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(28): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(19): Show |
1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(30): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(23): Show |
2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1460+2532_1460+253 others(34): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(25): Show |
3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0042 | 3 | HG02280.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1460+2532_1460+253 others(36): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(31): Show |
2 | a0002c0002t0001g0010a0002c0002t0008g0007 | 2 | HG02602.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1460+2532_1460+253 others(42): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(33): Show |
1 | a0002c0002t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(44): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(37): Show |
2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG00642.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1460+2532_1460+253 others(48): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(39): Show |
1 | a0002c0002t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(50): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | GATATATA others(41): Show |
1 | a0002c0002t0001g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(52): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 22413688 | |||||
| chr10:22413688
|
G | T | 8 | a0002c0002t0003g0113a0002c0002t0003g0114a0002c0002t0003g0128others(5): Show | 8 | HG01192.hp2 HG01243.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+2512G>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413688 | ||||||
| chr10:22413708
|
T | TATATATA others(4): Show |
1 | a0002c0002t0001g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(15): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413708 | ||||||
| chr10:22413708
|
T | TATATATA others(60): Show |
1 | a0001c0001t0005g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1460+2532_1460+253 others(71): Show |
SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413708 | ||||||
| chr10:22413745
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1460+2569T>C | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413745 | ||||||
| chr10:22413820
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0075 | 2 | HG01192.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1460+2644C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22413820 | ||||||
| chr10:22414008
|
A | G | 3 | a0002c0002t0003g0111a0002c0002t0003g0112a0002c0002t0003g0125 | 3 | HG03486.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1461-2611A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22414008 | ||||||
| chr10:22414211
|
A | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1461-2408A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22414211 | ||||||
| chr10:22414772
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1461-1847A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22414772 | ||||||
| chr10:22414787
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1461-1832A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22414787 | ||||||
| chr10:22415071
|
C | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123others(60): Show | 64 | HG00642.hp1 HG01071.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.1461-1548C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415071 | ||||||
| chr10:22415378
|
G | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1461-1241G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415378 | ||||||
| chr10:22415428
|
A | G | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461-1191A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415428 | ||||||
| chr10:22415604
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1461-1015G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415604 | ||||||
| chr10:22415704
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1461-915A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415704 | ||||||
| chr10:22415774
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0123 | 3 | HG00642.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1461-845C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415774 | ||||||
| chr10:22415905
|
G | A | 2 | a0002c0002t0006g0053a0002c0002t0006g0107 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1461-714G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415905 | ||||||
| chr10:22415963
|
G | A | 4 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461-656G>A | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22415963 | ||||||
| chr10:22416139
|
A | T | 20 | a0002c0002t0001g0068a0002c0002t0002g0004a0002c0002t0002g0013others(17): Show | 21 | HG01071.hp1 HG01175.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1461-480A>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22416139 | ||||||
| chr10:22416267
|
A | G | 1 | a0002c0002t0002g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1461-352A>G | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22416267 | ||||||
| chr10:22416290
|
C | T | 5 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0010others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1461-329C>T | SPAG6 | ENSG00000077327.16 | transcript | ENST00000376624.8 | protein_coding | 10/10 | chr10 | 22416290 |