Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10059 |
|---|---|
| ensemblid | ENSG00000087470.21 |
| hgncid | 2973 |
| symbol | DNM1L |
| name | dynamin 1 like |
| refseq_nuc | NM_012062.5 |
| refseq_prot | NP_036192.2 |
| ensembl_nuc | ENST00000549701.6 |
| ensembl_prot | ENSP00000450399.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 32679301 |
| end | 32745650 |
| strand | + |
| ver | v1.2 |
| region | chr12:32679301-32745650 |
| region5000 | chr12:32674301-32750650 |
| regionname0 | DNM1L_chr12_32679301_32745650 |
| regionname5000 | DNM1L_chr12_32674301_32750650 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 736 | 230 | 90 | 56 | 42 | 8 | 32 | 36 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2211 | 173 | 65 | 46 | 32 | 5 | 23 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| c0002 | 0/0 | 2211 | 43 | 19 | 8 | 9 | 2 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| c0003 | 0/0 | 2211 | 10 | 5 | 1 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| c0004 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| c0005 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| c0006 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2304 | 100 | 32 | 21 | 25 | 5 | 16 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0002 | 0/0 | 2304 | 40 | 16 | 9 | 8 | 2 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0003 | 0/0 | 2305 | 24 | 1 | 16 | 3 | 0 | 4 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0004 | 0/0 | 2304 | 10 | 9 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0005 | 0/0 | 2304 | 6 | 3 | 3 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0006 | 0/0 | 2306 | 6 | 3 | 0 | 1 | 0 | 2 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0007 | 0/0 | 2304 | 5 | 4 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0008 | 0/0 | 2305 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0009 | 0/0 | 2304 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0010 | 0/0 | 2307 | 4 | 0 | 0 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0011 | 0/0 | 2304 | 4 | 4 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0012 | 0/1 | 2304 | 4 | 1 | 2 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0013 | 0/0 | 2304 | 3 | 3 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0014 | 0/0 | 2305 | 2 | 2 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0015 | 0/0 | 2306 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0016 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0017 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0018 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0019 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0020 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0021 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0022 | 0/0 | 2304 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0023 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0024 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| t0025 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2211 | 173 | 65 | 46 | 32 | 5 | 23 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0002 | 0/0 | 2211 | 43 | 19 | 8 | 9 | 2 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0003 | 0/0 | 2211 | 10 | 5 | 1 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0004 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0005 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0006 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4514 | 99 | 32 | 21 | 25 | 5 | 15 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0003 | 0/0 | 4515 | 24 | 1 | 16 | 3 | 0 | 4 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0004 | 0/0 | 4514 | 9 | 8 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0005 | 0/0 | 4514 | 6 | 3 | 3 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0006 | 0/0 | 4516 | 6 | 3 | 0 | 1 | 0 | 2 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0008 | 0/0 | 4515 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0009 | 0/0 | 4514 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0011 | 0/0 | 4514 | 4 | 4 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0012 | 0/1 | 4514 | 4 | 1 | 2 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0014 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0015 | 0/0 | 4516 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0019 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0020 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0021 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0022 | 0/0 | 4514 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0023 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0024 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0001t0025 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0002t0002 | 0/0 | 4514 | 38 | 16 | 8 | 8 | 1 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0002t0013 | 0/0 | 4514 | 3 | 3 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0002t0016 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0002t0017 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0003t0007 | 0/0 | 4514 | 5 | 4 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0003t0010 | 0/0 | 4517 | 4 | 0 | 0 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0003t0018 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0004t0002 | 0/0 | 4514 | 2 | 0 | 1 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0005t0001 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| a0001c0006t0004 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | copy fasta | chr12 | 32674301 | 32750650 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0015g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0019g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0020g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0021g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0022g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0023g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0024g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0016g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0017g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0018g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0004t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0006t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0017 | g0024 | EUR | GBR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0104 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00738 | hp1 | a0001 | c0001 | t0012 | g0118 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00738 | hp2 | a0001 | c0001 | t0025 | g0223 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00741 | hp1 | a0001 | c0001 | t0024 | g0010 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0018 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01175 | hp2 | a0001 | c0003 | t0007 | g0215 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01361 | hp2 | a0001 | c0001 | t0022 | g0100 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01515 | hp1 | a0001 | c0004 | t0002 | g0037 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0026 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0224 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02129 | hp2 | a0001 | c0001 | t0020 | g0162 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02132 | hp2 | a0001 | c0003 | t0010 | g0217 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0206 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02572 | hp2 | a0001 | c0003 | t0007 | g0211 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0192 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0054 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02683 | hp1 | a0001 | c0001 | t0023 | g0015 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0053 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02809 | hp1 | a0001 | c0003 | t0018 | g0214 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0193 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02886 | hp1 | a0001 | c0003 | t0007 | g0210 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0208 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0207 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0142 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03041 | hp2 | a0001 | c0003 | t0007 | g0213 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03130 | hp1 | a0001 | c0002 | t0013 | g0045 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0144 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0226 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0194 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0202 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0154 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03834 | hp2 | a0001 | c0003 | t0010 | g0216 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03927 | hp1 | a0001 | c0003 | t0010 | g0218 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0227 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0121 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04204 | hp1 | a0001 | c0003 | t0010 | g0219 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0038 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18906 | hp2 | a0001 | c0003 | t0007 | g0212 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18942 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19002 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0047 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19063 | hp1 | a0001 | c0002 | t0016 | g0017 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ASW | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0205 | AFR | ASW | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02559 | hp1 | a0001 | c0006 | t0004 | g0014 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0086 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0119 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20300 | hp2 | a0001 | c0002 | t0013 | g0046 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0103 | REF | REF | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:32701432
|
A | C | 2 | a0001c0002a0001c0004 | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
synonymous_variant | LOW | c.120A>C | p.Ser40Ser | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/20 | 183/4514 | 120/2211 | 40/736 | chr12 | 32701432 | ||
| chr12:32707368
|
G | A | 3 | a0001c0002a0001c0003a0001c0004 | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
splice_region_variant&synonymous_variant | LOW | c.252G>A | p.Gly84Gly | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 3/20 | 315/4514 | 252/2211 | 84/736 | chr12 | 32707368 | ||
| chr12:32722472
|
A | G | 2 | a0001c0002a0001c0004 | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
synonymous_variant | LOW | c.918A>G | p.Thr306Thr | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/20 | 981/4514 | 918/2211 | 306/736 | chr12 | 32722472 | ||
| chr12:32722520
|
C | T | 1 | a0001c0006 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.966C>T | p.Tyr322Tyr | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/20 | 1029/4514 | 966/2211 | 322/736 | chr12 | 32722520 | ||
| chr12:32733738
|
A | G | 1 | a0001c0005 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1470A>G | p.Glu490Glu | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/20 | 1533/4514 | 1470/2211 | 490/736 | chr12 | 32733738 | ||
| chr12:32740492
|
C | T | 1 | a0001c0004 | 2 | HG01109.hp1 HG01515.hp1 |
synonymous_variant | LOW | c.1968C>T | p.Leu656Leu | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/20 | 2031/4514 | 1968/2211 | 656/736 | chr12 | 32740492 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:32679305
|
G | T | 1 | a0001c0001t0025 | 1 | HG00738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/20 | 59 | chr12 | 32679305 | |||||
| chr12:32679332
|
G | T | 3 | a0001c0001t0004a0001c0001t0024a0001c0006t0004 | 11 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/20 | chr12 | 32679332 | ||||||
| chr12:32743431
|
G | C | 8 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(5): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 21 | chr12 | 32743431 | |||||
| chr12:32743432
|
A | T | 8 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(5): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*22A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 22 | chr12 | 32743432 | |||||
| chr12:32743537
|
T | C | 1 | a0001c0002t0016 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 127 | chr12 | 32743537 | |||||
| chr12:32743538
|
A | G | 1 | a0001c0001t0015 | 2 | NA18942.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 128 | chr12 | 32743538 | |||||
| chr12:32743681
|
C | G | 8 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(5): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*271C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 271 | chr12 | 32743681 | |||||
| chr12:32743743
|
A | ATCTT | 1 | a0001c0003t0010 | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*335_*338dupCTTT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 339 | INFO_REALIGN_3_PRIME | chr12 | 32743743 | ||||
| chr12:32743803
|
A | C | 2 | a0001c0003t0007a0001c0003t0018 | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 393 | chr12 | 32743803 | |||||
| chr12:32744010
|
C | T | 1 | a0001c0001t0012 | 4 | HG00733.hp2 HG00738.hp1 NA20300.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*600C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 600 | chr12 | 32744010 | |||||
| chr12:32744154
|
A | T | 8 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(5): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*744A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 744 | chr12 | 32744154 | |||||
| chr12:32744274
|
C | T | 1 | a0001c0001t0023 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 864 | chr12 | 32744274 | |||||
| chr12:32744503
|
T | C | 13 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(10): Show | 76 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1093T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1093 | chr12 | 32744503 | |||||
| chr12:32744520
|
C | T | 1 | a0001c0001t0022 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1110C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1110 | chr12 | 32744520 | |||||
| chr12:32744530
|
A | G | 1 | a0001c0002t0017 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1120A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1120 | chr12 | 32744530 | |||||
| chr12:32744566
|
G | C | 3 | a0001c0003t0007a0001c0003t0010a0001c0003t0018 | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1156 | chr12 | 32744566 | |||||
| chr12:32744623
|
G | T | 8 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(5): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1213G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1213 | chr12 | 32744623 | |||||
| chr12:32744652
|
G | A | 5 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(2): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1242G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1242 | chr12 | 32744652 | |||||
| chr12:32744679
|
C | T | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1269C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1269 | chr12 | 32744679 | |||||
| chr12:32744709
|
G | A | 1 | a0001c0001t0019 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1299G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1299 | chr12 | 32744709 | |||||
| chr12:32744713
|
C | CA | 5 | a0001c0001t0003a0001c0001t0008a0001c0001t0014others(2): Show | 33 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1315dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1316 | INFO_REALIGN_3_PRIME | chr12 | 32744713 | ||||
| chr12:32744748
|
C | T | 1 | a0001c0003t0010 | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1338C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1338 | chr12 | 32744748 | |||||
| chr12:32744811
|
A | G | 1 | a0001c0001t0020 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1401 | chr12 | 32744811 | |||||
| chr12:32744825
|
T | C | 1 | a0001c0001t0009 | 5 | HG01884.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1415T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1415 | chr12 | 32744825 | |||||
| chr12:32744901
|
A | T | 1 | a0001c0001t0014 | 2 | HG02257.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1491A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1491 | chr12 | 32744901 | |||||
| chr12:32744947
|
AC | A | 1 | a0001c0003t0010 | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1538delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1538 | chr12 | 32744947 | |||||
| chr12:32745086
|
C | T | 1 | a0001c0003t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1676C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1676 | chr12 | 32745086 | |||||
| chr12:32745282
|
G | A | 1 | a0001c0003t0010 | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1872G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1872 | chr12 | 32745282 | |||||
| chr12:32745309
|
C | T | 1 | a0001c0001t0011 | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1899C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 1899 | chr12 | 32745309 | |||||
| chr12:32745511
|
C | CTT | 2 | a0001c0001t0006a0001c0001t0015 | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2102_*2103dupTT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 20/20 | 2104 | INFO_REALIGN_3_PRIME | chr12 | 32745511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:32679533
|
TGCCCACT others(11): Show |
T | 11 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(8): Show | 11 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+87_102+104delG others(17): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32679533 | |||||
| chr12:32679794
|
C | T | 1 | a0001c0002t0002g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102+329C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679794 | ||||||
| chr12:32679837
|
C | T | 13 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+372C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679837 | ||||||
| chr12:32679874
|
T | A | 1 | a0001c0001t0023g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.102+409T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679874 | ||||||
| chr12:32679913
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.102+448A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679913 | ||||||
| chr12:32679935
|
G | C | 59 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(56): Show | 60 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.102+470G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679935 | ||||||
| chr12:32679939
|
C | T | 75 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(72): Show | 76 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.102+474C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679939 | ||||||
| chr12:32679963
|
T | G | 76 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(73): Show | 77 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.102+498T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32679963 | ||||||
| chr12:32680055
|
T | TA | 13 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(10): Show | 13 | HG01175.hp2 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+590_102+591ins others(1): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680055 | ||||||
| chr12:32680056
|
T | A | 76 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(73): Show | 77 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.102+591T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680056 | ||||||
| chr12:32680066
|
A | G | 2 | a0001c0001t0006g0202a0001c0001t0006g0203 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.102+601A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680066 | ||||||
| chr12:32680126
|
G | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+661G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680126 | ||||||
| chr12:32680211
|
A | AT | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+755dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32680211 | |||||
| chr12:32680221
|
G | T | 70 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(67): Show | 71 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.102+756G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680221 | ||||||
| chr12:32680224
|
T | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+759T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680224 | ||||||
| chr12:32680224
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.102+759T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680224 | ||||||
| chr12:32680246
|
CTG | C | 2 | a0001c0002t0002g0071a0001c0002t0002g0072 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.102+783_102+784del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32680246 | |||||
| chr12:32680341
|
T | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+876T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680341 | ||||||
| chr12:32680414
|
G | T | 21 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(18): Show | 21 | HG01167.hp1 HG01175.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+949G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680414 | ||||||
| chr12:32680418
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.102+953G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680418 | ||||||
| chr12:32680513
|
CGTTT | C | 26 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(23): Show | 26 | HG01175.hp2 HG02055.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.102+1065_102+1068d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32680513 | |||||
| chr12:32680575
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.102+1110A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680575 | ||||||
| chr12:32680957
|
A | G | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+1492A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32680957 | ||||||
| chr12:32681214
|
T | C | 2 | a0001c0001t0004g0008a0001c0001t0004g0009 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.102+1749T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681214 | ||||||
| chr12:32681366
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.102+1901C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681366 | ||||||
| chr12:32681384
|
T | C | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+1919T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681384 | ||||||
| chr12:32681387
|
C | T | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+1922C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681387 | ||||||
| chr12:32681411
|
C | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+1946C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681411 | ||||||
| chr12:32681412
|
A | G | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+1947A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681412 | ||||||
| chr12:32681518
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102+2053C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681518 | ||||||
| chr12:32681530
|
A | AAGAG | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.102+2071_102+2074d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32681530 | |||||
| chr12:32681565
|
G | GC | 31 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0074others(28): Show | 31 | HG01099.hp2 HG01109.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.102+2108dupC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32681565 | |||||
| chr12:32681596
|
G | GC | 14 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+2138dupC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32681596 | |||||
| chr12:32681610
|
G | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+2145G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681610 | ||||||
| chr12:32681611
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+2146C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681611 | ||||||
| chr12:32681631
|
G | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2166G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681631 | ||||||
| chr12:32681668
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102+2203A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681668 | ||||||
| chr12:32681795
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.102+2330A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681795 | ||||||
| chr12:32681917
|
C | G | 7 | a0001c0002t0002g0051a0001c0002t0002g0052a0001c0002t0002g0053others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+2452C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681917 | ||||||
| chr12:32681996
|
C | A | 54 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+2531C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681996 | ||||||
| chr12:32681997
|
C | A | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+2532C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32681997 | ||||||
| chr12:32682137
|
G | GT | 6 | a0001c0001t0001g0196a0001c0001t0005g0088a0001c0003t0010g0216others(3): Show | 6 | HG01192.hp2 HG02132.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+2684dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32682137 | |||||
| chr12:32682147
|
T | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2682T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682147 | ||||||
| chr12:32682156
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+2691G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682156 | ||||||
| chr12:32682166
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+2701C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682166 | ||||||
| chr12:32682189
|
G | A | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+2724G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682189 | ||||||
| chr12:32682235
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02074.hp1 HG02132.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2770T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682235 | ||||||
| chr12:32682293
|
C | T | 7 | a0001c0001t0008g0073a0001c0003t0007g0210a0001c0003t0007g0211others(4): Show | 7 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+2828C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682293 | ||||||
| chr12:32682359
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.102+2894C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682359 | ||||||
| chr12:32682375
|
A | G | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+2910A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682375 | ||||||
| chr12:32682449
|
C | A | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+2984C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682449 | ||||||
| chr12:32682469
|
C | T | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+3004C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682469 | ||||||
| chr12:32682499
|
T | G | 55 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+3034T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682499 | ||||||
| chr12:32682817
|
A | G | 30 | a0001c0001t0001g0056a0001c0001t0003g0080a0001c0001t0003g0092others(27): Show | 30 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.102+3352A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682817 | ||||||
| chr12:32682830
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.102+3365A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32682830 | ||||||
| chr12:32683383
|
A | AT | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+3929dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32683383 | |||||
| chr12:32683406
|
C | T | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+3941C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683406 | ||||||
| chr12:32683490
|
G | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+4025G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683490 | ||||||
| chr12:32683531
|
GATTTT | G | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+4080_102+4084d others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32683531 | |||||
| chr12:32683786
|
A | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+4321A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683786 | ||||||
| chr12:32683881
|
G | A | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+4416G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683881 | ||||||
| chr12:32683956
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+4491G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683956 | ||||||
| chr12:32683969
|
C | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+4504C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32683969 | ||||||
| chr12:32684048
|
T | G | 1 | a0001c0001t0022g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.102+4583T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684048 | ||||||
| chr12:32684066
|
C | A | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.102+4601C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684066 | ||||||
| chr12:32684150
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.102+4685C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684150 | ||||||
| chr12:32684348
|
G | A | 1 | a0001c0002t0002g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+4883G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684348 | ||||||
| chr12:32684376
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+4911T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684376 | ||||||
| chr12:32684477
|
C | CT | 11 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(8): Show | 11 | HG02109.hp2 HG02132.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.102+5023dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32684477 | |||||
| chr12:32684477
|
C | CTTT | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.102+5021_102+5023d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32684477 | |||||
| chr12:32684489
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+5024C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684489 | ||||||
| chr12:32684600
|
C | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+5135C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684600 | ||||||
| chr12:32684665
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.102+5200T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684665 | ||||||
| chr12:32684707
|
G | T | 6 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(3): Show | 6 | HG02280.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+5242G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684707 | ||||||
| chr12:32684783
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+5318C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684783 | ||||||
| chr12:32684906
|
C | T | 114 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(111): Show | 116 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.102+5441C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684906 | ||||||
| chr12:32684911
|
A | C | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102+5446A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684911 | ||||||
| chr12:32684941
|
A | ATT | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+5491_102+5492d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32684941 | |||||
| chr12:32684943
|
T | TA | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+5478_102+5479i others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32684943 | ||||||
| chr12:32685021
|
G | C | 1 | a0001c0002t0002g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102+5556G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685021 | ||||||
| chr12:32685044
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+5579G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685044 | ||||||
| chr12:32685096
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.102+5631C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685096 | ||||||
| chr12:32685219
|
G | A | 3 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218 | 3 | HG02132.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.102+5754G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685219 | ||||||
| chr12:32685332
|
C | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+5867C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685332 | ||||||
| chr12:32685359
|
C | CT | 117 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0059others(114): Show | 118 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(115): Show |
intron_variant | MODIFIER | c.102+5913dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32685359 | |||||
| chr12:32685359
|
C | CTT | 18 | a0001c0001t0001g0085a0001c0001t0001g0160a0001c0001t0001g0161others(15): Show | 18 | HG01168.hp2 HG01346.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.102+5912_102+5913d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32685359 | |||||
| chr12:32685359
|
CTTT | C | 43 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(40): Show | 44 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.102+5911_102+5913d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32685359 | |||||
| chr12:32685400
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.102+5935G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685400 | ||||||
| chr12:32685416
|
T | A | 129 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.102+5951T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685416 | ||||||
| chr12:32685446
|
T | C | 129 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.102+5981T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685446 | ||||||
| chr12:32685550
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.102+6085C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685550 | ||||||
| chr12:32685594
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+6129C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685594 | ||||||
| chr12:32685645
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6180G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685645 | ||||||
| chr12:32685733
|
C | CT | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6278dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32685733 | |||||
| chr12:32685827
|
T | C | 78 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(75): Show | 79 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.102+6362T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685827 | ||||||
| chr12:32685851
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.102+6386C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32685851 | ||||||
| chr12:32685964
|
C | CT | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6506dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32685964 | |||||
| chr12:32686045
|
C | CT | 27 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0081others(24): Show | 27 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.102+6602dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686045 | |||||
| chr12:32686045
|
C | CTT | 45 | a0001c0001t0001g0158a0001c0001t0003g0189a0001c0001t0006g0203others(42): Show | 46 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.102+6601_102+6602d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686045 | |||||
| chr12:32686045
|
C | CTTT | 10 | a0001c0001t0004g0012a0001c0001t0008g0073a0001c0001t0008g0204others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+6600_102+6602d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686045 | |||||
| chr12:32686045
|
C | CTTTTT | 5 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0007others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+6598_102+6602d others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686045 | |||||
| chr12:32686112
|
G | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6647G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686112 | ||||||
| chr12:32686129
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18952.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.102+6664C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686129 | ||||||
| chr12:32686178
|
G | A | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+6713G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686178 | ||||||
| chr12:32686180
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+6715A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686180 | ||||||
| chr12:32686338
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6873T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686338 | ||||||
| chr12:32686359
|
T | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6894T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686359 | ||||||
| chr12:32686360
|
T | A | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+6895T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686360 | ||||||
| chr12:32686382
|
T | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+6917T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686382 | ||||||
| chr12:32686436
|
C | T | 2 | a0001c0001t0004g0012a0001c0006t0004g0014 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.102+6971C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686436 | ||||||
| chr12:32686446
|
C | CTG | 130 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(127): Show | 132 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.102+6982_102+6983i others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686446 | |||||
| chr12:32686466
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+7001C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686466 | ||||||
| chr12:32686603
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7138T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686603 | ||||||
| chr12:32686607
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+7142G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686607 | ||||||
| chr12:32686821
|
T | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7356T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686821 | ||||||
| chr12:32686854
|
C | G | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.102+7389C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686854 | ||||||
| chr12:32686885
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7420A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686885 | ||||||
| chr12:32686928
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+7472_102+7483d others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686928 | |||||
| chr12:32686928
|
CTTTTTTT others(8): Show |
C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+7472_102+7486d others(17): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686928 | |||||
| chr12:32686928
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0002t0002g0071a0001c0002t0002g0072 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.102+7472_102+7487d others(18): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686928 | |||||
| chr12:32686932
|
TTTTTC | T | 40 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(37): Show | 41 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.102+7472_102+7476d others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686932 | |||||
| chr12:32686937
|
C | CT | 67 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(64): Show | 68 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.102+7491dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32686937 | |||||
| chr12:32686941
|
T | C | 1 | a0001c0001t0005g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.102+7476T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686941 | ||||||
| chr12:32686942
|
T | TC | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+7477_102+7478i others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686942 | ||||||
| chr12:32686959
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7494G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32686959 | ||||||
| chr12:32687113
|
A | G | 1 | a0001c0002t0002g0020 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.102+7648A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687113 | ||||||
| chr12:32687161
|
T | C | 15 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.102+7696T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687161 | ||||||
| chr12:32687173
|
T | TTGTGA | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7709_102+7710i others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32687173 | |||||
| chr12:32687176
|
A | G | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+7711A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687176 | ||||||
| chr12:32687246
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7781C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687246 | ||||||
| chr12:32687254
|
T | G | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+7789T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687254 | ||||||
| chr12:32687310
|
G | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7845G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687310 | ||||||
| chr12:32687350
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7885C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687350 | ||||||
| chr12:32687446
|
T | TTTG | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+7994_102+7996d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32687446 | |||||
| chr12:32687474
|
A | G | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+8009A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687474 | ||||||
| chr12:32687502
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8037A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687502 | ||||||
| chr12:32687594
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+8129C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687594 | ||||||
| chr12:32687620
|
A | AT | 6 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0224others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+8164dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32687620 | |||||
| chr12:32687701
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.102+8236C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687701 | ||||||
| chr12:32687743
|
C | G | 20 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.102+8278C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687743 | ||||||
| chr12:32687854
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8389C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32687854 | ||||||
| chr12:32688075
|
C | G | 3 | a0001c0002t0013g0045a0001c0002t0013g0046a0001c0002t0013g0047 | 3 | HG03130.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102+8610C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688075 | ||||||
| chr12:32688126
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8661C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688126 | ||||||
| chr12:32688172
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8707A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688172 | ||||||
| chr12:32688176
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8711T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688176 | ||||||
| chr12:32688211
|
C | CA | 2 | a0001c0001t0014g0205a0001c0001t0014g0206 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.102+8747dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32688211 | |||||
| chr12:32688215
|
G | C | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+8750G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688215 | ||||||
| chr12:32688226
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8761G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688226 | ||||||
| chr12:32688334
|
C | T | 2 | a0001c0001t0012g0118a0001c0001t0012g0119 | 2 | HG00738.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.102+8869C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688334 | ||||||
| chr12:32688360
|
G | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+8895G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688360 | ||||||
| chr12:32688473
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0021g0154 | 2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.102+9008C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688473 | ||||||
| chr12:32688592
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9127G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688592 | ||||||
| chr12:32688624
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+9159T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688624 | ||||||
| chr12:32688632
|
C | G | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+9167C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688632 | ||||||
| chr12:32688653
|
T | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+9188T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688653 | ||||||
| chr12:32688878
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.102+9413G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32688878 | ||||||
| chr12:32689112
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+9647T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689112 | ||||||
| chr12:32689121
|
T | A | 1 | a0001c0001t0008g0207 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102+9656T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689121 | ||||||
| chr12:32689142
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.102+9677T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689142 | ||||||
| chr12:32689192
|
C | CTATTT | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9744_102+9748d others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32689192 | |||||
| chr12:32689283
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9818T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689283 | ||||||
| chr12:32689308
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9843C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689308 | ||||||
| chr12:32689322
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+9857C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689322 | ||||||
| chr12:32689328
|
G | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9863G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689328 | ||||||
| chr12:32689389
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+9924G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689389 | ||||||
| chr12:32689426
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+9961T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689426 | ||||||
| chr12:32689435
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+9970C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689435 | ||||||
| chr12:32689483
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+10018C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689483 | ||||||
| chr12:32689627
|
T | TAA | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+10162_102+1016 others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689627 | ||||||
| chr12:32689664
|
AGAATT | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+10202_102+1020 others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32689664 | |||||
| chr12:32689732
|
G | A | 3 | a0001c0001t0003g0177a0001c0001t0003g0187a0001c0001t0003g0189 | 3 | NA18944.hp1 NA19004.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.102+10267G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689732 | ||||||
| chr12:32689822
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102+10357C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689822 | ||||||
| chr12:32689911
|
C | T | 2 | a0001c0001t0005g0079a0001c0001t0005g0088 | 2 | HG01192.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.102+10446C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689911 | ||||||
| chr12:32689942
|
G | C | 129 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.102+10477G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32689942 | ||||||
| chr12:32690035
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.102+10570A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690035 | ||||||
| chr12:32690087
|
T | C | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.102+10622T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690087 | ||||||
| chr12:32690288
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+10823A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690288 | ||||||
| chr12:32690455
|
G | C | 1 | a0001c0002t0017g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.103-10960G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690455 | ||||||
| chr12:32690706
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-10709C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690706 | ||||||
| chr12:32690837
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-10578G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690837 | ||||||
| chr12:32690934
|
C | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-10481C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690934 | ||||||
| chr12:32690969
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-10446C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32690969 | ||||||
| chr12:32691088
|
A | G | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-10327A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691088 | ||||||
| chr12:32691152
|
C | T | 61 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(58): Show | 62 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-10263C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691152 | ||||||
| chr12:32691242
|
G | A | 53 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(50): Show | 54 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.103-10173G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691242 | ||||||
| chr12:32691279
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-10136G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691279 | ||||||
| chr12:32691300
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-10115G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691300 | ||||||
| chr12:32691301
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-10114C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691301 | ||||||
| chr12:32691703
|
G | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-9712G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691703 | ||||||
| chr12:32691736
|
T | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-9679T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691736 | ||||||
| chr12:32691739
|
T | C | 1 | a0001c0001t0022g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.103-9676T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691739 | ||||||
| chr12:32691752
|
AG | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-9662delG | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691752 | ||||||
| chr12:32691772
|
A | G | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.103-9643A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691772 | ||||||
| chr12:32691833
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-9582G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691833 | ||||||
| chr12:32691864
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.103-9551G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32691864 | ||||||
| chr12:32692015
|
A | AC | 130 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(127): Show | 132 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.103-9400_103-9399i others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692015 | ||||||
| chr12:32692036
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-9379T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692036 | ||||||
| chr12:32692216
|
T | C | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-9199T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692216 | ||||||
| chr12:32692288
|
C | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-9127C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692288 | ||||||
| chr12:32692548
|
C | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-8867C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692548 | ||||||
| chr12:32692615
|
AAC | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-8796_103-8795d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32692615 | |||||
| chr12:32692646
|
G | GT | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-8763dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32692646 | |||||
| chr12:32692672
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-8743A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692672 | ||||||
| chr12:32692897
|
TC | T | 7 | a0001c0002t0002g0051a0001c0002t0002g0052a0001c0002t0002g0053others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-8515delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32692897 | |||||
| chr12:32692984
|
T | C | 6 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0224others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-8431T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32692984 | ||||||
| chr12:32693011
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-8404C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693011 | ||||||
| chr12:32693065
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-8350T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693065 | ||||||
| chr12:32693338
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-8077G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693338 | ||||||
| chr12:32693472
|
G | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-7943G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693472 | ||||||
| chr12:32693542
|
A | T | 25 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(22): Show | 26 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.103-7873A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693542 | ||||||
| chr12:32693588
|
GT | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-7819delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32693588 | |||||
| chr12:32693762
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-7653C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693762 | ||||||
| chr12:32693838
|
A | G | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.103-7577A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693838 | ||||||
| chr12:32693928
|
C | T | 4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-7487C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693928 | ||||||
| chr12:32693980
|
C | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-7435C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693980 | ||||||
| chr12:32693996
|
T | C | 1 | a0001c0001t0020g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.103-7419T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32693996 | ||||||
| chr12:32694049
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-7366A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694049 | ||||||
| chr12:32694230
|
T | C | 64 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(61): Show | 65 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.103-7185T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694230 | ||||||
| chr12:32694285
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.103-7130C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694285 | ||||||
| chr12:32694308
|
A | G | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-7107A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694308 | ||||||
| chr12:32694317
|
C | G | 2 | a0001c0001t0004g0008a0001c0001t0004g0009 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.103-7098C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694317 | ||||||
| chr12:32694345
|
A | G | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-7070A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694345 | ||||||
| chr12:32694373
|
C | T | 3 | a0001c0002t0013g0045a0001c0002t0013g0046a0001c0002t0013g0047 | 3 | HG03130.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.103-7042C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694373 | ||||||
| chr12:32694414
|
A | G | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.103-7001A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694414 | ||||||
| chr12:32694421
|
A | G | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-6994A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694421 | ||||||
| chr12:32694478
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6937T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694478 | ||||||
| chr12:32694567
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6848C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694567 | ||||||
| chr12:32694675
|
T | A | 25 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(22): Show | 26 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.103-6740T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694675 | ||||||
| chr12:32694770
|
C | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6645C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694770 | ||||||
| chr12:32694804
|
C | G | 1 | a0001c0001t0004g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.103-6611C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694804 | ||||||
| chr12:32694813
|
T | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6602T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694813 | ||||||
| chr12:32694928
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6487C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32694928 | ||||||
| chr12:32695034
|
CAAG | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-6374_103-6372d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32695034 | |||||
| chr12:32695138
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-6277C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695138 | ||||||
| chr12:32695174
|
A | G | 3 | a0001c0001t0003g0095a0001c0001t0003g0185a0001c0001t0003g0186 | 3 | HG01070.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.103-6241A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695174 | ||||||
| chr12:32695220
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0201 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.103-6195A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695220 | ||||||
| chr12:32695419
|
C | T | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.103-5996C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695419 | ||||||
| chr12:32695446
|
A | T | 6 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5969A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695446 | ||||||
| chr12:32695590
|
G | A | 1 | a0001c0001t0003g0178 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.103-5825G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695590 | ||||||
| chr12:32695591
|
G | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-5824G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695591 | ||||||
| chr12:32695645
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-5770C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695645 | ||||||
| chr12:32695646
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.103-5769G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32695646 | ||||||
| chr12:32695806
|
CAA | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5606_103-5605d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32695806 | |||||
| chr12:32696303
|
A | G | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.103-5112A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696303 | ||||||
| chr12:32696373
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.103-5032_103-5023d others(12): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696373 | |||||
| chr12:32696383
|
A | AAC | 68 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(65): Show | 68 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.103-5000_103-4999d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696383
|
A | AACAC | 38 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0098others(35): Show | 38 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.103-5002_103-4999d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696383
|
A | AACACAC | 11 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0003g0080others(8): Show | 12 | HG00738.hp2 HG01099.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-5004_103-4999d others(8): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696383
|
A | AC | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0021g0154 | 3 | HG03688.hp1 HG03688.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.103-5032_103-5031i others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696383 | ||||||
| chr12:32696383
|
A | ACAC | 3 | a0001c0001t0001g0151a0001c0001t0001g0195a0001c0001t0001g0220 | 3 | HG01074.hp1 HG01074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.103-5032_103-5031i others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696383 | ||||||
| chr12:32696383
|
AAC | A | 9 | a0001c0001t0001g0085a0001c0001t0001g0165a0001c0001t0001g0166others(6): Show | 9 | HG00733.hp2 HG01346.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-5000_103-4999d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696383
|
AACAC | A | 51 | a0001c0001t0001g0164a0001c0002t0002g0001a0001c0002t0002g0016others(48): Show | 52 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.103-5002_103-4999d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696383
|
AACACAC | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0197a0001c0001t0004g0004others(3): Show | 6 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5004_103-4999d others(8): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696383 | |||||
| chr12:32696387
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.103-5028C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696387 | ||||||
| chr12:32696392
|
A | ACT | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5022_103-5021i others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696392 | |||||
| chr12:32696398
|
A | T | 50 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(47): Show | 51 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.103-5017A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696398 | ||||||
| chr12:32696442
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-4973G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696442 | ||||||
| chr12:32696468
|
G | A | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-4947G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696468 | ||||||
| chr12:32696600
|
T | TA | 5 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-4803dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696600 | |||||
| chr12:32696600
|
TA | T | 18 | a0001c0001t0003g0095a0001c0001t0004g0004a0001c0001t0004g0005others(15): Show | 18 | HG01167.hp1 HG01168.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.103-4803delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696600 | |||||
| chr12:32696600
|
TAA | T | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.103-4804_103-4803d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696600 | |||||
| chr12:32696634
|
C | CT | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.103-4771dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696634 | |||||
| chr12:32696660
|
A | C | 58 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(55): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-4755A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696660 | ||||||
| chr12:32696670
|
A | AGG | 58 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(55): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-4745_103-4744i others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696670 | ||||||
| chr12:32696671
|
A | C | 58 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(55): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-4744A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696671 | ||||||
| chr12:32696675
|
C | A | 58 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(55): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-4740C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696675 | ||||||
| chr12:32696700
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-4715C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696700 | ||||||
| chr12:32696767
|
G | C | 4 | a0001c0002t0002g0021a0001c0002t0002g0025a0001c0002t0002g0048others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-4648G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696767 | ||||||
| chr12:32696781
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-4634C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696781 | ||||||
| chr12:32696835
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.103-4580G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696835 | ||||||
| chr12:32696867
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-4548T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696867 | ||||||
| chr12:32696872
|
AC | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-4541delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32696872 | |||||
| chr12:32696876
|
C | A | 2 | a0001c0001t0009g0221a0001c0001t0009g0222 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.103-4539C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696876 | ||||||
| chr12:32696914
|
C | T | 1 | a0001c0001t0011g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.103-4501C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696914 | ||||||
| chr12:32696918
|
A | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-4497A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696918 | ||||||
| chr12:32696921
|
G | A | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-4494G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696921 | ||||||
| chr12:32696938
|
C | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-4477C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696938 | ||||||
| chr12:32696954
|
A | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-4461A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696954 | ||||||
| chr12:32696975
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.103-4440C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696975 | ||||||
| chr12:32696991
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.103-4424G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32696991 | ||||||
| chr12:32697002
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-4413C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697002 | ||||||
| chr12:32697236
|
A | T | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.103-4179A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697236 | ||||||
| chr12:32697278
|
A | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-4137A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697278 | ||||||
| chr12:32697450
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3965A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697450 | ||||||
| chr12:32697489
|
C | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-3926C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697489 | ||||||
| chr12:32697675
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.103-3740G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697675 | ||||||
| chr12:32697726
|
CAAG | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-3688_103-3686d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697726 | ||||||
| chr12:32697854
|
A | G | 7 | a0001c0001t0005g0079a0001c0001t0005g0088a0001c0001t0005g0090others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-3561A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697854 | ||||||
| chr12:32697867
|
T | C | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-3548T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697867 | ||||||
| chr12:32697912
|
A | C | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-3503A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32697912 | ||||||
| chr12:32697983
|
A | AT | 55 | a0001c0001t0001g0120a0001c0001t0004g0004a0001c0001t0004g0005others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.103-3420dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32697983 | |||||
| chr12:32698124
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-3291G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698124 | ||||||
| chr12:32698258
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.103-3157G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698258 | ||||||
| chr12:32698430
|
G | A | 19 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.103-2985G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698430 | ||||||
| chr12:32698446
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2969T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698446 | ||||||
| chr12:32698483
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2932T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698483 | ||||||
| chr12:32698529
|
T | G | 8 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 8 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-2886T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698529 | ||||||
| chr12:32698654
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2761G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698654 | ||||||
| chr12:32698703
|
A | AAC | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2711_103-2710i others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32698703 | |||||
| chr12:32698899
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2516C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698899 | ||||||
| chr12:32698932
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.103-2483G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32698932 | ||||||
| chr12:32699001
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2414T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699001 | ||||||
| chr12:32699005
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2410A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699005 | ||||||
| chr12:32699026
|
A | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-2389A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699026 | ||||||
| chr12:32699075
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2340C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699075 | ||||||
| chr12:32699076
|
G | A | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-2339G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699076 | ||||||
| chr12:32699102
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-2313A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699102 | ||||||
| chr12:32699271
|
C | T | 4 | a0001c0001t0006g0172a0001c0001t0006g0202a0001c0001t0006g0203others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-2144C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699271 | ||||||
| chr12:32699272
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2143G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699272 | ||||||
| chr12:32699311
|
TAAA | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-2101_103-2099d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699311 | |||||
| chr12:32699345
|
T | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-2070T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699345 | ||||||
| chr12:32699608
|
G | C | 114 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(111): Show | 116 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.103-1807G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699608 | ||||||
| chr12:32699648
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.103-1767G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699648 | ||||||
| chr12:32699669
|
C | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-1746C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699669 | ||||||
| chr12:32699677
|
T | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1738T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699677 | ||||||
| chr12:32699796
|
C | CA | 116 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(113): Show | 117 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.103-1596dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699796 | |||||
| chr12:32699796
|
C | CAA | 9 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG01261.hp1 HG02074.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-1597_103-1596d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699796 | |||||
| chr12:32699796
|
CA | C | 5 | a0001c0001t0001g0163a0001c0001t0004g0005a0001c0001t0004g0006others(2): Show | 5 | HG00733.hp2 HG01167.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-1596delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699796 | |||||
| chr12:32699796
|
CAAAAAAA | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-1602_103-1596d others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699796 | |||||
| chr12:32699796
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-1603_103-1596d others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699796 | |||||
| chr12:32699803
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1612A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699803 | ||||||
| chr12:32699804
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-1611A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699804 | ||||||
| chr12:32699805
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-1610A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699805 | ||||||
| chr12:32699817
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1598A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699817 | ||||||
| chr12:32699833
|
A | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-1582A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699833 | ||||||
| chr12:32699946
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-1469A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32699946 | ||||||
| chr12:32699975
|
C | CTAAATCT others(1): Show |
54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-1439_103-1432d others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32699975 | |||||
| chr12:32700015
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-1400A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700015 | ||||||
| chr12:32700052
|
GCAAAAAC | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-1353_103-1347d others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32700052 | |||||
| chr12:32700139
|
GAGA | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-1273_103-1271d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32700139 | |||||
| chr12:32700207
|
C | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-1208C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700207 | ||||||
| chr12:32700223
|
A | G | 129 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.103-1192A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700223 | ||||||
| chr12:32700337
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1078C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700337 | ||||||
| chr12:32700356
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103-1059A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700356 | ||||||
| chr12:32700417
|
G | C | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-998G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700417 | ||||||
| chr12:32700597
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.103-818T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700597 | ||||||
| chr12:32700599
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-816G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700599 | ||||||
| chr12:32700607
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.103-808T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700607 | ||||||
| chr12:32700663
|
G | A | 7 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(4): Show | 7 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-752G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700663 | ||||||
| chr12:32700777
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-638A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700777 | ||||||
| chr12:32700821
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-594A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700821 | ||||||
| chr12:32700837
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.103-578A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700837 | ||||||
| chr12:32700850
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.103-565G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32700850 | ||||||
| chr12:32701017
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103-398C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701017 | ||||||
| chr12:32701065
|
G | C | 4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-350G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701065 | ||||||
| chr12:32701104
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103-311G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701104 | ||||||
| chr12:32701143
|
G | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-272G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701143 | ||||||
| chr12:32701148
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-267C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701148 | ||||||
| chr12:32701200
|
C | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-215C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701200 | ||||||
| chr12:32701217
|
A | G | 224 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(221): Show | 226 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(223): Show |
intron_variant | MODIFIER | c.103-198A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701217 | ||||||
| chr12:32701263
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103-152C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701263 | ||||||
| chr12:32701266
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-149A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701266 | ||||||
| chr12:32701271
|
C | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-144C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701271 | ||||||
| chr12:32701276
|
C | CA | 21 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0126others(18): Show | 21 | HG00741.hp2 HG01346.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-124dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32701276 | |||||
| chr12:32701276
|
CA | C | 11 | a0001c0001t0001g0155a0001c0003t0007g0210a0001c0003t0007g0211others(8): Show | 11 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-124delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 32701276 | |||||
| chr12:32701292
|
T | A | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-123T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 1/19 | chr12 | 32701292 | ||||||
| chr12:32701668
|
G | A | 225 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(222): Show | 227 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(224): Show |
intron_variant | MODIFIER | c.250+106G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701668 | ||||||
| chr12:32701709
|
T | TA | 50 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(47): Show | 51 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.250+155dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32701709 | |||||
| chr12:32701753
|
G | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+191G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701753 | ||||||
| chr12:32701818
|
A | T | 1 | a0001c0001t0022g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250+256A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701818 | ||||||
| chr12:32701824
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+262T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701824 | ||||||
| chr12:32701884
|
T | C | 72 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(69): Show | 73 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.250+322T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701884 | ||||||
| chr12:32701965
|
C | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+403C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701965 | ||||||
| chr12:32702007
|
G | A | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+445G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702007 | ||||||
| chr12:32702146
|
A | G | 7 | a0001c0001t0003g0093a0001c0001t0003g0176a0001c0001t0003g0178others(4): Show | 7 | HG00733.hp1 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+584A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702146 | ||||||
| chr12:32702233
|
C | CA | 21 | a0001c0001t0001g0077a0001c0001t0001g0147a0001c0001t0003g0186others(18): Show | 22 | HG01070.hp1 HG01167.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+692dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702233 | |||||
| chr12:32702233
|
C | CAA | 31 | a0001c0001t0001g0056a0001c0001t0001g0169a0001c0001t0001g0170others(28): Show | 31 | HG00733.hp1 HG00738.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.250+691_250+692dup others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702233 | |||||
| chr12:32702233
|
C | CAAA | 8 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+690_250+692dup others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702233 | |||||
| chr12:32702233
|
CA | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0001t0001g0198others(7): Show | 10 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+692delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702233 | |||||
| chr12:32702233
|
CAAA | C | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+690_250+692del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702233 | |||||
| chr12:32702353
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+791C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702353 | ||||||
| chr12:32702403
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.250+841G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702403 | ||||||
| chr12:32702438
|
A | G | 21 | a0001c0001t0003g0080a0001c0001t0003g0092a0001c0001t0003g0093others(18): Show | 21 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.250+876A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702438 | ||||||
| chr12:32702461
|
T | C | 4 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+899T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702461 | ||||||
| chr12:32702501
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+939A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702501 | ||||||
| chr12:32702510
|
G | A | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250+948G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702510 | ||||||
| chr12:32702580
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+1018T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702580 | ||||||
| chr12:32702656
|
T | C | 8 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(5): Show | 8 | HG02132.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+1094T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702656 | ||||||
| chr12:32702685
|
A | AT | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.250+1133dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702685 | |||||
| chr12:32702685
|
A | ATT | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+1132_250+1133d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702685 | |||||
| chr12:32702963
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.250+1401T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32702963 | ||||||
| chr12:32702977
|
C | CACTA | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+1418_250+1419i others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32702977 | |||||
| chr12:32703041
|
GTCTTTCT others(1): Show |
G | 43 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(40): Show | 44 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.250+1483_250+1490d others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703041 | |||||
| chr12:32703045
|
T | C | 1 | a0001c0002t0002g0026 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.250+1483T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703045 | ||||||
| chr12:32703045
|
TTCTC | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG00741.hp2 HG01934.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+1493_250+1496d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703045 | |||||
| chr12:32703056
|
TC | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+1495delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703056 | ||||||
| chr12:32703057
|
C | CT | 12 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0126others(9): Show | 12 | HG01168.hp2 HG01346.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.250+1509dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703057 | |||||
| chr12:32703057
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+1495C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703057 | ||||||
| chr12:32703057
|
CT | C | 16 | a0001c0001t0001g0151a0001c0001t0001g0220a0001c0001t0003g0186others(13): Show | 16 | HG01070.hp1 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.250+1509delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703057 | |||||
| chr12:32703377
|
G | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.250+1815G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703377 | ||||||
| chr12:32703481
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+1919C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703481 | ||||||
| chr12:32703491
|
A | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+1929A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703491 | ||||||
| chr12:32703600
|
G | GA | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.250+2041dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703600 | |||||
| chr12:32703614
|
C | CA | 10 | a0001c0001t0001g0081a0001c0001t0001g0126a0001c0001t0001g0150others(7): Show | 10 | HG01515.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+2070dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703614 | |||||
| chr12:32703614
|
C | CAA | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2069_250+2070d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703614 | |||||
| chr12:32703614
|
CA | C | 59 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0078others(56): Show | 60 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.250+2070delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703614 | |||||
| chr12:32703614
|
CAA | C | 10 | a0001c0002t0002g0016a0001c0002t0002g0026a0001c0002t0002g0032others(7): Show | 10 | HG01516.hp2 HG02132.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+2069_250+2070d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32703614 | |||||
| chr12:32703702
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.250+2140C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703702 | ||||||
| chr12:32703797
|
A | C | 1 | a0001c0002t0002g0039 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.250+2235A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703797 | ||||||
| chr12:32703832
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+2270A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32703832 | ||||||
| chr12:32704271
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+2709C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704271 | ||||||
| chr12:32704365
|
C | A | 15 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.250+2803C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704365 | ||||||
| chr12:32704366
|
G | A | 107 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(104): Show | 108 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.250+2804G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704366 | ||||||
| chr12:32704524
|
TG | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2840delG | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32704524 | |||||
| chr12:32704549
|
TA | T | 120 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(117): Show | 120 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(117): Show |
intron_variant | MODIFIER | c.251-2802delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32704549 | |||||
| chr12:32704549
|
TAA | T | 47 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(44): Show | 48 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.251-2803_251-2802d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32704549 | |||||
| chr12:32704560
|
A | G | 1 | a0001c0001t0025g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.251-2807A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704560 | ||||||
| chr12:32704583
|
C | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-2784C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704583 | ||||||
| chr12:32704584
|
G | A | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-2783G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704584 | ||||||
| chr12:32704630
|
AT | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-2734delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32704630 | |||||
| chr12:32704638
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.251-2729A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704638 | ||||||
| chr12:32704847
|
T | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-2520T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704847 | ||||||
| chr12:32704853
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0196 | 2 | HG01071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.251-2514A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704853 | ||||||
| chr12:32704912
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.251-2455G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32704912 | ||||||
| chr12:32705000
|
G | GT | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(66): Show | 70 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.251-2344dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32705000 | |||||
| chr12:32705000
|
G | GTT | 20 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0067others(17): Show | 20 | HG00733.hp2 HG00741.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.251-2345_251-2344d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32705000 | |||||
| chr12:32705000
|
GT | G | 12 | a0001c0001t0001g0102a0001c0001t0008g0204a0001c0001t0008g0207others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2344delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr12 | 32705000 | |||||
| chr12:32705011
|
T | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2356T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705011 | ||||||
| chr12:32705050
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2317G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705050 | ||||||
| chr12:32705148
|
G | A | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-2219G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705148 | ||||||
| chr12:32705261
|
T | C | 15 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.251-2106T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705261 | ||||||
| chr12:32705369
|
T | C | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.251-1998T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705369 | ||||||
| chr12:32705480
|
A | G | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-1887A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705480 | ||||||
| chr12:32705506
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.251-1861C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705506 | ||||||
| chr12:32705682
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.251-1685C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705682 | ||||||
| chr12:32705728
|
A | G | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.251-1639A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705728 | ||||||
| chr12:32705959
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.251-1408C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32705959 | ||||||
| chr12:32706122
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.251-1245A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706122 | ||||||
| chr12:32706134
|
C | G | 1 | a0001c0001t0003g0094 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.251-1233C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706134 | ||||||
| chr12:32706173
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1194G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706173 | ||||||
| chr12:32706183
|
A | T | 1 | a0001c0001t0015g0003 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.251-1184A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706183 | ||||||
| chr12:32706265
|
C | T | 8 | a0001c0002t0002g0019a0001c0002t0002g0023a0001c0002t0002g0034others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-1102C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706265 | ||||||
| chr12:32706473
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-894A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706473 | ||||||
| chr12:32706477
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.251-890C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706477 | ||||||
| chr12:32706709
|
T | G | 1 | a0001c0001t0006g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.251-658T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706709 | ||||||
| chr12:32706757
|
G | T | 8 | a0001c0002t0002g0019a0001c0002t0002g0023a0001c0002t0002g0034others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-610G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706757 | ||||||
| chr12:32706823
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.251-544C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706823 | ||||||
| chr12:32706889
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.251-478C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706889 | ||||||
| chr12:32706912
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.251-455G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32706912 | ||||||
| chr12:32707032
|
T | C | 3 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0013 | 3 | HG01891.hp1 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.251-335T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32707032 | ||||||
| chr12:32707524
|
T | A | 1 | a0001c0002t0002g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.297+111T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 3/19 | chr12 | 32707524 | ||||||
| chr12:32707749
|
A | G | 1 | a0001c0001t0004g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.297+336A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 3/19 | chr12 | 32707749 | ||||||
| chr12:32707812
|
G | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.298-341G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 3/19 | chr12 | 32707812 | ||||||
| chr12:32707929
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.298-224T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 3/19 | chr12 | 32707929 | ||||||
| chr12:32708336
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+112A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32708336 | ||||||
| chr12:32708402
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+178A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32708402 | ||||||
| chr12:32708475
|
T | C | 4 | a0001c0001t0006g0172a0001c0001t0006g0202a0001c0001t0006g0203others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+251T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32708475 | ||||||
| chr12:32708677
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.369+453T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32708677 | ||||||
| chr12:32708770
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+546G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32708770 | ||||||
| chr12:32709020
|
G | A | 1 | a0001c0001t0006g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.369+796G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709020 | ||||||
| chr12:32709200
|
T | C | 1 | a0001c0002t0002g0027 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.369+976T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709200 | ||||||
| chr12:32709229
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.369+1005C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709229 | ||||||
| chr12:32709375
|
G | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.369+1151G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709375 | ||||||
| chr12:32709403
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.369+1179A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709403 | ||||||
| chr12:32709405
|
A | C | 1 | a0001c0001t0009g0225 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.369+1181A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709405 | ||||||
| chr12:32709643
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.370-1286T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709643 | ||||||
| chr12:32709816
|
A | G | 3 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218 | 3 | HG02132.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.370-1113A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709816 | ||||||
| chr12:32709839
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.370-1090G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709839 | ||||||
| chr12:32709937
|
A | G | 5 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0224others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-992A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709937 | ||||||
| chr12:32709951
|
A | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-978A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709951 | ||||||
| chr12:32709961
|
T | G | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.370-968T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32709961 | ||||||
| chr12:32710047
|
CAG | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-881_370-880del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710047 | ||||||
| chr12:32710089
|
A | T | 2 | a0001c0001t0009g0221a0001c0001t0009g0222 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.370-840A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710089 | ||||||
| chr12:32710587
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-342C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710587 | ||||||
| chr12:32710618
|
C | CA | 5 | a0001c0001t0001g0075a0001c0001t0001g0120a0001c0001t0003g0093others(2): Show | 5 | HG01891.hp1 HG01928.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-295dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 32710618 | |||||
| chr12:32710618
|
CA | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(2): Show | 5 | HG01167.hp1 HG01167.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-295delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 32710618 | |||||
| chr12:32710618
|
CAA | C | 11 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(8): Show | 11 | HG02109.hp2 HG02132.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-296_370-295del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 32710618 | |||||
| chr12:32710618
|
CAAA | C | 50 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(47): Show | 51 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.370-297_370-295del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 32710618 | |||||
| chr12:32710691
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-238A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710691 | ||||||
| chr12:32710766
|
A | G | 2 | a0001c0001t0003g0080a0001c0001t0003g0094 | 2 | HG01099.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.370-163A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710766 | ||||||
| chr12:32710890
|
T | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-39T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 4/19 | chr12 | 32710890 | ||||||
| chr12:32711306
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.456+291C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711306 | ||||||
| chr12:32711366
|
G | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+351G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711366 | ||||||
| chr12:32711433
|
A | G | 2 | a0001c0001t0004g0008a0001c0001t0004g0009 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.456+418A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711433 | ||||||
| chr12:32711462
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+447A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711462 | ||||||
| chr12:32711506
|
T | A | 2 | a0001c0001t0014g0205a0001c0001t0014g0206 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.456+491T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711506 | ||||||
| chr12:32711525
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.456+510C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711525 | ||||||
| chr12:32711559
|
GC | G | 3 | a0001c0002t0013g0045a0001c0002t0013g0046a0001c0002t0013g0047 | 3 | HG03130.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.456+545delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711559 | ||||||
| chr12:32711593
|
G | A | 72 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(69): Show | 73 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.456+578G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711593 | ||||||
| chr12:32711816
|
G | A | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.456+801G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711816 | ||||||
| chr12:32711874
|
C | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+859C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32711874 | ||||||
| chr12:32712115
|
G | A | 1 | a0001c0002t0002g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457-1094G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712115 | ||||||
| chr12:32712151
|
T | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-1058T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712151 | ||||||
| chr12:32712458
|
A | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-751A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712458 | ||||||
| chr12:32712537
|
C | T | 4 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-672C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712537 | ||||||
| chr12:32712649
|
C | CA | 50 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(47): Show | 50 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.457-531dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 32712649 | |||||
| chr12:32712649
|
C | CAA | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0120others(4): Show | 7 | HG01928.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.457-532_457-531dup others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 32712649 | |||||
| chr12:32712649
|
CAA | C | 7 | a0001c0002t0002g0021a0001c0002t0002g0029a0001c0002t0002g0050others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.457-532_457-531del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 32712649 | |||||
| chr12:32712649
|
CAAA | C | 40 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(37): Show | 41 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.457-533_457-531del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 32712649 | |||||
| chr12:32712672
|
A | AG | 3 | a0001c0001t0003g0095a0001c0001t0003g0185a0001c0001t0003g0186 | 3 | HG01070.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.457-537_457-536ins others(1): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712672 | ||||||
| chr12:32712688
|
C | G | 1 | a0001c0001t0025g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.457-521C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712688 | ||||||
| chr12:32712920
|
A | C | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.457-289A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712920 | ||||||
| chr12:32712964
|
A | G | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.457-245A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712964 | ||||||
| chr12:32712981
|
C | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0094 | 2 | HG01099.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.457-228C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32712981 | ||||||
| chr12:32713129
|
T | C | 1 | a0001c0001t0004g0006 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.457-80T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 5/19 | chr12 | 32713129 | ||||||
| chr12:32713465
|
G | A | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.619+94G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713465 | ||||||
| chr12:32713469
|
T | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.619+98T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713469 | ||||||
| chr12:32713582
|
A | T | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.619+211A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713582 | ||||||
| chr12:32713623
|
G | A | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.619+252G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713623 | ||||||
| chr12:32713724
|
C | G | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.619+353C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713724 | ||||||
| chr12:32713878
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.619+507C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32713878 | ||||||
| chr12:32714270
|
A | AT | 5 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0003g0092others(2): Show | 5 | HG01071.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.619+919dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32714270 | |||||
| chr12:32714270
|
AT | A | 17 | a0001c0001t0001g0058a0001c0001t0004g0011a0001c0001t0004g0012others(14): Show | 17 | HG01175.hp2 HG01884.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.619+919delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32714270 | |||||
| chr12:32714270
|
ATT | A | 44 | a0001c0001t0009g0222a0001c0002t0002g0001a0001c0002t0002g0016others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.619+918_619+919del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32714270 | |||||
| chr12:32714279
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.619+908T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714279 | ||||||
| chr12:32714301
|
C | A | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.619+930C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714301 | ||||||
| chr12:32714429
|
C | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.619+1058C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714429 | ||||||
| chr12:32714462
|
C | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.619+1091C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714462 | ||||||
| chr12:32714533
|
G | A | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.619+1162G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714533 | ||||||
| chr12:32714625
|
A | T | 14 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(11): Show | 15 | HG00639.hp2 HG01123.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.619+1254A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32714625 | ||||||
| chr12:32714825
|
T | TA | 40 | a0001c0001t0001g0061a0001c0001t0001g0169a0001c0001t0001g0170others(37): Show | 40 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.619+1466dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32714825 | |||||
| chr12:32715004
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.619+1633A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715004 | ||||||
| chr12:32715093
|
C | CT | 55 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0082others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.619+1738dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32715093 | |||||
| chr12:32715093
|
CT | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.619+1738delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32715093 | |||||
| chr12:32715304
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.619+1933A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715304 | ||||||
| chr12:32715333
|
T | C | 5 | a0001c0002t0002g0020a0001c0002t0002g0030a0001c0002t0002g0039others(2): Show | 5 | NA18953.hp1 NA18985.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+1962T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715333 | ||||||
| chr12:32715361
|
G | A | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619+1990G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715361 | ||||||
| chr12:32715566
|
C | A | 2 | a0001c0001t0006g0202a0001c0001t0006g0203 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.619+2195C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715566 | ||||||
| chr12:32715680
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.619+2309C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715680 | ||||||
| chr12:32715729
|
CA | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.619+2367delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32715729 | |||||
| chr12:32715754
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.619+2383C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715754 | ||||||
| chr12:32715775
|
A | G | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.619+2404A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32715775 | ||||||
| chr12:32716242
|
T | TG | 92 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(89): Show | 93 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.620-2392dupG | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716242 | |||||
| chr12:32716242
|
T | TGG | 15 | a0001c0001t0001g0056a0001c0001t0001g0062a0001c0001t0001g0067others(12): Show | 15 | HG00140.hp1 HG00639.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.620-2393_620-2392d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716242 | |||||
| chr12:32716252
|
T | C | 1 | a0001c0001t0022g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.620-2391T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716252 | ||||||
| chr12:32716371
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-2272G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716371 | ||||||
| chr12:32716517
|
C | T | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-2126C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716517 | ||||||
| chr12:32716538
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.620-2105C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716538 | ||||||
| chr12:32716701
|
T | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-1942T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716701 | ||||||
| chr12:32716742
|
G | GTA | 49 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0001g0159others(46): Show | 50 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.620-1880_620-1879d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716742 | |||||
| chr12:32716742
|
G | GTATA | 32 | a0001c0001t0001g0171a0001c0001t0001g0198a0001c0001t0001g0201others(29): Show | 32 | HG00733.hp1 HG01070.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.620-1882_620-1879d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716742 | |||||
| chr12:32716742
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-1886_620-1879d others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716742 | |||||
| chr12:32716742
|
GTA | G | 15 | a0001c0001t0003g0179a0001c0001t0006g0172a0001c0001t0006g0173others(12): Show | 16 | HG01081.hp1 HG01175.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-1880_620-1879d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716742 | |||||
| chr12:32716742
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-1886_620-1879d others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32716742 | |||||
| chr12:32716794
|
A | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-1849A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716794 | ||||||
| chr12:32716995
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.620-1648C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32716995 | ||||||
| chr12:32717075
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-1568A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717075 | ||||||
| chr12:32717088
|
T | A | 8 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(5): Show | 9 | HG02074.hp2 HG02683.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.620-1555T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717088 | ||||||
| chr12:32717090
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0004g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.620-1534_620-1516d others(21): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717090 | |||||
| chr12:32717119
|
T | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1524T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717119 | ||||||
| chr12:32717120
|
TTA | T | 51 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(48): Show | 52 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.620-1514_620-1513d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717120 | |||||
| chr12:32717122
|
A | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1521A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717122 | ||||||
| chr12:32717198
|
TTTA | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1443_620-1441d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717198 | |||||
| chr12:32717214
|
A | AATATATA others(20): Show |
1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.620-1415_620-1414i others(29): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717214 | |||||
| chr12:32717221
|
AG | A | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-1421delG | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717221 | ||||||
| chr12:32717229
|
T | C | 63 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(60): Show | 64 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.620-1414T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717229 | ||||||
| chr12:32717229
|
TTATATAT others(402): Show |
T | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-1409_620-1001d others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717229 | |||||
| chr12:32717240
|
T | TTATATAT others(2): Show |
4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1385_620-1377d others(11): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717240 | |||||
| chr12:32717258
|
GTATATAT others(31): Show |
G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1376_620-1339d others(40): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717258 | |||||
| chr12:32717291
|
ATATT | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1350_620-1347d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717291 | |||||
| chr12:32717294
|
T | C | 1 | a0001c0002t0002g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.620-1349T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717294 | ||||||
| chr12:32717296
|
T | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1347T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717296 | ||||||
| chr12:32717309
|
A | G | 4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-1334A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717309 | ||||||
| chr12:32717311
|
A | G | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.620-1332A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717311 | ||||||
| chr12:32717313
|
T | A | 19 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.620-1330T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717313 | ||||||
| chr12:32717314
|
A | C | 19 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.620-1329A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717314 | ||||||
| chr12:32717319
|
TAC | T | 26 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(23): Show | 26 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.620-1321_620-1320d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717319 | |||||
| chr12:32717321
|
CACTATAT others(20): Show |
C | 24 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(21): Show | 25 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.620-1321_620-1295d others(29): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717321 | ||||||
| chr12:32717331
|
T | A | 26 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(23): Show | 26 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.620-1312T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717331 | ||||||
| chr12:32717332
|
T | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1311T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717332 | ||||||
| chr12:32717332
|
T | C | 20 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(17): Show | 20 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.620-1311T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717332 | ||||||
| chr12:32717340
|
ACTATATA others(81): Show |
A | 19 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.620-1302_620-1215d others(90): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717340 | ||||||
| chr12:32717341
|
CTATATAT | C | 5 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.620-1294_620-1288d others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717341 | |||||
| chr12:32717341
|
CTATATAT others(103): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.620-1293_620-1184d others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717341 | |||||
| chr12:32717349
|
T | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1294T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717349 | ||||||
| chr12:32717356
|
AGTATATA others(65): Show |
A | 1 | a0001c0002t0002g0044 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.620-1286_620-1215d others(74): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717356 | ||||||
| chr12:32717357
|
G | C | 35 | a0001c0001t0008g0073a0001c0002t0002g0001a0001c0002t0002g0016others(32): Show | 36 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.620-1286G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717357 | ||||||
| chr12:32717365
|
A | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1278A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717365 | ||||||
| chr12:32717365
|
AAT | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-1270_620-1269d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717365 | |||||
| chr12:32717366
|
A | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1277A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717366 | ||||||
| chr12:32717383
|
A | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1260A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717383 | ||||||
| chr12:32717383
|
AATATATA others(38): Show |
A | 24 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(21): Show | 25 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.620-1252_620-1208d others(47): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717383 | |||||
| chr12:32717391
|
G | C | 20 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(17): Show | 20 | HG01167.hp1 HG01175.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.620-1252G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717391 | ||||||
| chr12:32717399
|
A | AATATATA others(4): Show |
1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1237_620-1236i others(13): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717399 | |||||
| chr12:32717399
|
AATATATA others(22): Show |
A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1236_620-1208d others(31): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717399 | |||||
| chr12:32717406
|
AATATATA others(15): Show |
A | 64 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(61): Show | 64 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.620-1194_620-1173d others(24): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717406 | |||||
| chr12:32717407
|
A | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1236A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717407 | ||||||
| chr12:32717414
|
T | C | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1229T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717414 | ||||||
| chr12:32717414
|
TTTTAAAT others(6): Show |
T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1227_620-1215d others(15): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717414 | |||||
| chr12:32717416
|
T | A | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1227T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717416 | ||||||
| chr12:32717419
|
A | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1224A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717419 | ||||||
| chr12:32717427
|
C | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.620-1216C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717427 | ||||||
| chr12:32717428
|
T | A | 5 | a0001c0001t0008g0073a0001c0003t0010g0216a0001c0003t0010g0217others(2): Show | 5 | HG02132.hp2 HG02970.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.620-1215T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717428 | ||||||
| chr12:32717441
|
AATATATA others(37): Show |
A | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1194_620-1151d others(46): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717441 | |||||
| chr12:32717514
|
G | C | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-1129G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717514 | ||||||
| chr12:32717552
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1091C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717552 | ||||||
| chr12:32717565
|
C | CAAATATA others(26): Show |
7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-1072_620-1040d others(35): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717565 | |||||
| chr12:32717565
|
C | CAAATATA others(125): Show |
3 | a0001c0003t0010g0217a0001c0003t0010g0218a0001c0003t0010g0219 | 3 | HG02132.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.620-1040_620-1039i others(134): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717565 | |||||
| chr12:32717565
|
C | CAAATATA others(158): Show |
1 | a0001c0003t0010g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.620-1040_620-1039i others(167): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717565 | |||||
| chr12:32717571
|
T | TATATACC others(26): Show |
7 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(4): Show | 7 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-907_620-875dup others(33): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717571 | |||||
| chr12:32717571
|
TATATACC others(26): Show |
T | 22 | a0001c0001t0001g0137a0001c0001t0001g0169a0001c0001t0001g0170others(19): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.620-907_620-875del others(33): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717571 | |||||
| chr12:32717571
|
TATATACC others(59): Show |
T | 25 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(22): Show | 26 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.620-940_620-875del others(66): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717571 | |||||
| chr12:32717588
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.620-1055A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717588 | ||||||
| chr12:32717604
|
C | T | 19 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(16): Show | 19 | HG01175.hp2 HG02109.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.620-1039C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717604 | ||||||
| chr12:32717637
|
C | T | 36 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(33): Show | 36 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.620-1006C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717637 | ||||||
| chr12:32717640
|
A | T | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-1003A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717640 | ||||||
| chr12:32717663
|
A | T | 4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-980A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717663 | ||||||
| chr12:32717670
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-973C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717670 | ||||||
| chr12:32717675
|
ACCTAGG | A | 6 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(3): Show | 7 | HG02074.hp2 HG03041.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-967_620-962del others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717675 | ||||||
| chr12:32717676
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.620-967C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717676 | ||||||
| chr12:32717677
|
C | A | 1 | a0001c0001t0006g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.620-966C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717677 | ||||||
| chr12:32717680
|
G | T | 1 | a0001c0001t0006g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.620-963G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717680 | ||||||
| chr12:32717681
|
G | A | 1 | a0001c0001t0006g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.620-962G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717681 | ||||||
| chr12:32717684
|
G | T | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-959G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717684 | ||||||
| chr12:32717696
|
A | AAAAATAT others(61): Show |
6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-941_620-940ins others(68): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717696 | |||||
| chr12:32717696
|
A | T | 6 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(3): Show | 7 | HG02074.hp2 HG03041.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-947A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717696 | ||||||
| chr12:32717697
|
AAAATAC | A | 4 | a0001c0001t0006g0173a0001c0001t0006g0174a0001c0001t0006g0175others(1): Show | 5 | HG03041.hp1 NA18942.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.620-944_620-939del others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717697 | |||||
| chr12:32717698
|
A | T | 2 | a0001c0001t0006g0172a0001c0001t0006g0202 | 2 | HG02074.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.620-945A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717698 | ||||||
| chr12:32717703
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-940C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717703 | ||||||
| chr12:32717736
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-907C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717736 | ||||||
| chr12:32717738
|
T | TATACCTA others(59): Show |
4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-875_620-874ins others(66): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717738 | |||||
| chr12:32717815
|
TATAAA | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-824_620-820del others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717815 | |||||
| chr12:32717830
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.620-813G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717830 | ||||||
| chr12:32717842
|
T | C | 1 | a0001c0001t0009g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.620-801T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717842 | ||||||
| chr12:32717847
|
TTTA | T | 8 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(5): Show | 8 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-794_620-792del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717847 | |||||
| chr12:32717848
|
T | TATATATA others(130): Show |
2 | a0001c0003t0010g0217a0001c0003t0010g0218 | 2 | HG02132.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.620-795_620-794ins others(137): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717848 | ||||||
| chr12:32717850
|
A | T | 2 | a0001c0003t0010g0217a0001c0003t0010g0218 | 2 | HG02132.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.620-793A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717850 | ||||||
| chr12:32717851
|
TAA | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-790_620-789del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717851 | |||||
| chr12:32717853
|
A | T | 20 | a0001c0001t0001g0074a0001c0001t0001g0165a0001c0001t0003g0184others(17): Show | 20 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.620-790A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717853 | ||||||
| chr12:32717881
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-762A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717881 | ||||||
| chr12:32717881
|
ATATT | A | 4 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-758_620-755del others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717881 | |||||
| chr12:32717896
|
A | ATAG | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-745_620-744ins others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717896 | |||||
| chr12:32717903
|
G | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-740G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717903 | ||||||
| chr12:32717903
|
GTATA | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-733_620-730del others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717903 | |||||
| chr12:32717903
|
GTATATAT others(24): Show |
G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.620-731_620-701del others(31): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717903 | |||||
| chr12:32717909
|
A | AC | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-734_620-733ins others(1): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717909 | ||||||
| chr12:32717911
|
A | AT | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-731dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717911 | |||||
| chr12:32717913
|
A | ATATATTT others(25): Show |
2 | a0001c0003t0010g0216a0001c0003t0010g0219 | 2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.620-730_620-729ins others(32): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717913 | ||||||
| chr12:32717913
|
A | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-730A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717913 | ||||||
| chr12:32717915
|
A | T | 8 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(5): Show | 8 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-728A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717915 | ||||||
| chr12:32717921
|
G | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-722G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717921 | ||||||
| chr12:32717927
|
ATT | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-713_620-712del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717927 | |||||
| chr12:32717928
|
T | TAAATATA | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-715_620-714ins others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717928 | ||||||
| chr12:32717930
|
T | A | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-713T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717930 | ||||||
| chr12:32717931
|
T | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-712T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717931 | ||||||
| chr12:32717932
|
A | AG | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-711_620-710ins others(1): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717932 | ||||||
| chr12:32717932
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-711A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717932 | ||||||
| chr12:32717944
|
A | AATATAGT others(20): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.620-680_620-654dup others(27): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717944 | |||||
| chr12:32717950
|
G | GTATATAT others(11): Show |
1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.620-675_620-658dup others(18): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717950 | |||||
| chr12:32717950
|
GTATATAT others(11): Show |
G | 3 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0007 | 3 | HG01167.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.620-675_620-658del others(18): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717950 | |||||
| chr12:32717955
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-688T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717955 | ||||||
| chr12:32717977
|
G | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0007 | 3 | HG01167.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.620-666G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717977 | ||||||
| chr12:32717978
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-665T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717978 | ||||||
| chr12:32717983
|
ATAG | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-657_620-655del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717983 | |||||
| chr12:32717986
|
G | A | 13 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(10): Show | 13 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.620-657G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32717986 | ||||||
| chr12:32717999
|
A | ATATT | 2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.620-641_620-640ins others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32717999 | |||||
| chr12:32718000
|
TATA | T | 8 | a0001c0002t0002g0019a0001c0002t0002g0023a0001c0002t0002g0034others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-639_620-637del others(3): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32718000 | |||||
| chr12:32718003
|
AAT | A | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-632_620-631del others(2): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32718003 | |||||
| chr12:32718004
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.620-639A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718004 | ||||||
| chr12:32718008
|
A | G | 56 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0002t0002g0001others(53): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.620-635A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718008 | ||||||
| chr12:32718008
|
A | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-635A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718008 | ||||||
| chr12:32718020
|
TA | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.620-622delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718020 | ||||||
| chr12:32718027
|
A | AT | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.620-616_620-615ins others(1): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718027 | ||||||
| chr12:32718040
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.620-603C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718040 | ||||||
| chr12:32718044
|
C | T | 56 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0002t0002g0001others(53): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.620-599C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718044 | ||||||
| chr12:32718081
|
ATATTT | A | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.620-558_620-554del others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 32718081 | |||||
| chr12:32718228
|
G | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-415G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718228 | ||||||
| chr12:32718297
|
G | A | 59 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0136others(56): Show | 60 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-346G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718297 | ||||||
| chr12:32718392
|
T | C | 45 | a0001c0001t0001g0129a0001c0002t0002g0001a0001c0002t0002g0016others(42): Show | 46 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.620-251T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718392 | ||||||
| chr12:32718438
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.620-205G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718438 | ||||||
| chr12:32718464
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0003g0112 | 2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.620-179A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718464 | ||||||
| chr12:32718467
|
A | G | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.620-176A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718467 | ||||||
| chr12:32718531
|
A | G | 1 | a0001c0001t0003g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.620-112A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718531 | ||||||
| chr12:32718547
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.620-96G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718547 | ||||||
| chr12:32718555
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-88G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 6/19 | chr12 | 32718555 | ||||||
| chr12:32718891
|
C | T | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740+128C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32718891 | ||||||
| chr12:32718926
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.740+163G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32718926 | ||||||
| chr12:32718945
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+182A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32718945 | ||||||
| chr12:32718954
|
A | AT | 6 | a0001c0001t0001g0169a0001c0001t0004g0004a0001c0001t0004g0005others(3): Show | 6 | HG01167.hp1 HG02818.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+206dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr12 | 32718954 | |||||
| chr12:32718954
|
AT | A | 52 | a0001c0001t0003g0186a0001c0001t0004g0008a0001c0001t0020g0162others(49): Show | 53 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.740+206delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr12 | 32718954 | |||||
| chr12:32719091
|
T | C | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.740+328T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719091 | ||||||
| chr12:32719100
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+337A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719100 | ||||||
| chr12:32719126
|
T | G | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.740+363T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719126 | ||||||
| chr12:32719507
|
G | T | 129 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.740+744G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719507 | ||||||
| chr12:32719565
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.740+802A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719565 | ||||||
| chr12:32719677
|
T | C | 1 | a0001c0001t0015g0003 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.740+914T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719677 | ||||||
| chr12:32719778
|
G | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.741-886G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719778 | ||||||
| chr12:32719828
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.741-836A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719828 | ||||||
| chr12:32719858
|
T | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.741-806T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719858 | ||||||
| chr12:32719913
|
T | A | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.741-751T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32719913 | ||||||
| chr12:32720002
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-662G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32720002 | ||||||
| chr12:32720057
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.741-607T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32720057 | ||||||
| chr12:32720305
|
A | G | 1 | a0001c0001t0022g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.741-359A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32720305 | ||||||
| chr12:32720456
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.741-208G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32720456 | ||||||
| chr12:32720645
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-19G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 7/19 | chr12 | 32720645 | ||||||
| chr12:32720922
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18952.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.872+127G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32720922 | ||||||
| chr12:32720923
|
T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18952.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.872+128T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32720923 | ||||||
| chr12:32720982
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.872+187C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32720982 | ||||||
| chr12:32721079
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.872+284C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721079 | ||||||
| chr12:32721323
|
AC | A | 2 | a0001c0002t0002g0016a0001c0002t0002g0029 | 2 | NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.872+529delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721323 | ||||||
| chr12:32721370
|
G | T | 1 | a0001c0001t0004g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.872+575G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721370 | ||||||
| chr12:32721390
|
G | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.872+595G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721390 | ||||||
| chr12:32721431
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.872+636T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721431 | ||||||
| chr12:32721619
|
T | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-808T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721619 | ||||||
| chr12:32721706
|
G | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.873-721G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721706 | ||||||
| chr12:32721906
|
G | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-521G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721906 | ||||||
| chr12:32721966
|
G | T | 1 | a0001c0001t0025g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.873-461G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32721966 | ||||||
| chr12:32722118
|
T | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.873-309T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 8/19 | chr12 | 32722118 | ||||||
| chr12:32722788
|
G | A | 4 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+155G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32722788 | ||||||
| chr12:32722870
|
T | TTAAA | 51 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(48): Show | 52 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1079+239_1079+240i others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32722870 | |||||
| chr12:32722870
|
T | TTAAATAC others(21): Show |
3 | a0001c0002t0002g0030a0001c0002t0002g0050a0001c0002t0016g0017 | 3 | NA18953.hp1 NA18994.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1079+239_1079+240i others(30): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32722870 | |||||
| chr12:32723397
|
C | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+764C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723397 | ||||||
| chr12:32723574
|
A | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+941A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723574 | ||||||
| chr12:32723618
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+985C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723618 | ||||||
| chr12:32723646
|
A | T | 19 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1079+1013A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723646 | ||||||
| chr12:32723665
|
G | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+1032G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723665 | ||||||
| chr12:32723693
|
C | CA | 34 | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0001g0096others(31): Show | 34 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1079+1081dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32723693 | |||||
| chr12:32723693
|
CA | C | 10 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(7): Show | 10 | HG01167.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+1081delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32723693 | |||||
| chr12:32723693
|
CAAA | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+1079_1079+108 others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32723693 | |||||
| chr12:32723707
|
A | C | 2 | a0001c0001t0009g0221a0001c0001t0009g0222 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1079+1074A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723707 | ||||||
| chr12:32723708
|
A | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+1075A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32723708 | ||||||
| chr12:32723770
|
C | CCAAAA | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+1142_1079+114 others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32723770 | |||||
| chr12:32724030
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079+1397A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724030 | ||||||
| chr12:32724138
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+1505C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724138 | ||||||
| chr12:32724162
|
CTACTT | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+1532_1079+153 others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724162 | |||||
| chr12:32724247
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1079+1614C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724247 | ||||||
| chr12:32724332
|
C | G | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1079+1699C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724332 | ||||||
| chr12:32724499
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+1866C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724499 | ||||||
| chr12:32724530
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+1897C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724530 | ||||||
| chr12:32724576
|
CA | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0132others(5): Show | 8 | HG00741.hp2 HG03453.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+1961delA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724576 | |||||
| chr12:32724576
|
CAA | C | 22 | a0001c0001t0001g0089a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01074.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1079+1960_1079+196 others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724576 | |||||
| chr12:32724577
|
A | C | 6 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(3): Show | 6 | HG02280.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079+1944A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724577 | ||||||
| chr12:32724587
|
A | T | 1 | a0001c0006t0004g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1079+1954A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724587 | ||||||
| chr12:32724587
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0002t0002g0025a0001c0002t0002g0044a0001c0002t0002g0048others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079+1956_1079+196 others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724587 | |||||
| chr12:32724588
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0002t0016g0017 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1079+1957_1079+196 others(17): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724588 | |||||
| chr12:32724589
|
A | T | 2 | a0001c0001t0014g0205a0001c0006t0004g0014 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1079+1956A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724589 | ||||||
| chr12:32724589
|
AAAAAAT | A | 7 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0102others(4): Show | 7 | HG01361.hp1 HG02273.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+1958_1079+196 others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724589 | |||||
| chr12:32724589
|
AAAAAATA others(1): Show |
A | 5 | a0001c0001t0024g0010a0001c0002t0002g0051a0001c0002t0002g0052others(2): Show | 5 | HG00741.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+1958_1079+196 others(12): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724589 | |||||
| chr12:32724589
|
AAAAAATA others(3): Show |
A | 12 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(9): Show | 12 | HG00639.hp1 HG01515.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1079+1958_1079+196 others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724589 | |||||
| chr12:32724589
|
AAAAAATA others(5): Show |
A | 12 | a0001c0001t0004g0011a0001c0002t0002g0001a0001c0002t0002g0020others(9): Show | 13 | HG00639.hp2 HG01123.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1079+1958_1079+196 others(16): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724589 | |||||
| chr12:32724590
|
AAAAATAT others(2): Show |
A | 6 | a0001c0002t0017g0024a0001c0003t0007g0210a0001c0003t0007g0212others(3): Show | 6 | HG00140.hp1 HG01175.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079+1959_1079+196 others(13): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724590 | |||||
| chr12:32724591
|
A | ATAT | 2 | a0001c0001t0006g0173a0001c0001t0006g0175 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1079+1958_1079+195 others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724591 | ||||||
| chr12:32724591
|
A | T | 12 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0129others(9): Show | 12 | HG01884.hp2 HG01975.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1079+1958A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724591 | ||||||
| chr12:32724591
|
AAAATAT | A | 19 | a0001c0001t0001g0074a0001c0001t0001g0097a0001c0001t0001g0098others(16): Show | 19 | HG00140.hp2 HG00733.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1079+1960_1079+196 others(10): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724591 | |||||
| chr12:32724591
|
AAAATATA others(3): Show |
A | 4 | a0001c0002t0002g0033a0001c0002t0013g0045a0001c0002t0013g0046others(1): Show | 4 | HG01109.hp1 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079+1960_1079+196 others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724591 | |||||
| chr12:32724591
|
AAAATATA others(5): Show |
A | 2 | a0001c0002t0002g0016a0001c0002t0002g0030 | 2 | NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1079+1960_1079+197 others(16): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724591 | |||||
| chr12:32724593
|
A | T | 41 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0082others(38): Show | 41 | HG00741.hp2 HG01346.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.1079+1960A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724593 | ||||||
| chr12:32724593
|
AAT | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0125others(5): Show | 8 | HG01071.hp2 HG01167.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+1986_1079+198 others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724593 | |||||
| chr12:32724593
|
AATAT | A | 7 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0091others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+1984_1079+198 others(8): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724593 | |||||
| chr12:32724593
|
AATATATA others(3): Show |
A | 2 | a0001c0002t0013g0047a0001c0003t0010g0219 | 2 | HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1079+1978_1079+198 others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724593 | |||||
| chr12:32724594
|
AT | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0147a0001c0001t0008g0073 | 3 | HG02451.hp1 HG02970.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1079+1962delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724594 | ||||||
| chr12:32724594
|
ATAT | A | 3 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0007 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1079+1962_1079+196 others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724594 | ||||||
| chr12:32724594
|
ATATAT | A | 21 | a0001c0001t0003g0080a0001c0001t0003g0092a0001c0001t0003g0093others(18): Show | 21 | HG00733.hp1 HG01070.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1079+1962_1079+196 others(9): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724594 | ||||||
| chr12:32724595
|
T | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(13): Show | 16 | HG01074.hp2 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1079+1962T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724595 | ||||||
| chr12:32724597
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0004g0006 | 2 | HG01167.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1079+1964T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724597 | ||||||
| chr12:32724599
|
T | A | 6 | a0001c0001t0003g0177a0001c0001t0003g0179a0001c0001t0004g0004others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+1966T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724599 | ||||||
| chr12:32724601
|
T | A | 9 | a0001c0001t0003g0080a0001c0001t0003g0094a0001c0001t0003g0179others(6): Show | 9 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079+1968T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724601 | ||||||
| chr12:32724605
|
T | A | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1079+1972T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724605 | ||||||
| chr12:32724619
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0073 | 2 | HG02970.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1079+1986T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724619 | ||||||
| chr12:32724623
|
T | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+1990T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724623 | ||||||
| chr12:32724643
|
TTAAA | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1079+2013_1079+201 others(8): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724643 | |||||
| chr12:32724664
|
A | T | 72 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(69): Show | 73 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1079+2031A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724664 | ||||||
| chr12:32724665
|
A | T | 1 | a0001c0001t0006g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1079+2032A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724665 | ||||||
| chr12:32724680
|
TATA | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+2054_1079+205 others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32724680 | |||||
| chr12:32724908
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+2275A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32724908 | ||||||
| chr12:32725004
|
A | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+2371A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725004 | ||||||
| chr12:32725004
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0197 | 2 | HG03669.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1079+2371A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725004 | ||||||
| chr12:32725041
|
A | AT | 5 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(2): Show | 5 | HG01361.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079+2419dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32725041 | |||||
| chr12:32725073
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1079+2440A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725073 | ||||||
| chr12:32725075
|
TTTC | T | 58 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(55): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1079+2457_1079+245 others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32725075 | |||||
| chr12:32725116
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079+2483A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725116 | ||||||
| chr12:32725541
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+2908A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725541 | ||||||
| chr12:32725629
|
T | C | 114 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(111): Show | 116 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.1079+2996T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725629 | ||||||
| chr12:32725685
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079+3052A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725685 | ||||||
| chr12:32725752
|
C | T | 3 | a0001c0002t0002g0016a0001c0002t0002g0027a0001c0002t0002g0029 | 3 | HG02129.hp1 NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1079+3119C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725752 | ||||||
| chr12:32725780
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+3147G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725780 | ||||||
| chr12:32725866
|
A | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+3233A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725866 | ||||||
| chr12:32725910
|
G | GT | 13 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0089others(10): Show | 13 | HG00741.hp1 HG02132.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1079+3293dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32725910 | |||||
| chr12:32725910
|
GT | G | 51 | a0001c0001t0001g0064a0001c0001t0001g0141a0001c0001t0001g0151others(48): Show | 52 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1079+3293delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32725910 | |||||
| chr12:32725911
|
T | G | 1 | a0001c0001t0003g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1079+3278T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725911 | ||||||
| chr12:32725935
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+3302G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32725935 | ||||||
| chr12:32726000
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079+3367A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726000 | ||||||
| chr12:32726012
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1079+3379A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726012 | ||||||
| chr12:32726036
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1079+3403C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726036 | ||||||
| chr12:32726061
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1079+3428C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726061 | ||||||
| chr12:32726124
|
T | TAA | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1079+3493_1079+349 others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32726124 | |||||
| chr12:32726412
|
C | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1079+3779C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726412 | ||||||
| chr12:32726561
|
C | T | 1 | a0001c0002t0002g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1079+3928C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726561 | ||||||
| chr12:32726609
|
T | G | 30 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(27): Show | 30 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1079+3976T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726609 | ||||||
| chr12:32726624
|
C | G | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1079+3991C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726624 | ||||||
| chr12:32726672
|
T | C | 1 | a0001c0001t0009g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1079+4039T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32726672 | ||||||
| chr12:32727042
|
G | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1080-3972G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32727042 | ||||||
| chr12:32727164
|
C | G | 4 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-3850C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32727164 | ||||||
| chr12:32727195
|
TAGTAATC others(2): Show |
T | 2 | a0001c0001t0001g0089a0001c0001t0003g0130 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1080-3816_1080-380 others(13): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32727195 | |||||
| chr12:32727497
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-3517C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32727497 | ||||||
| chr12:32727529
|
G | GA | 8 | a0001c0001t0001g0155a0001c0002t0013g0045a0001c0002t0013g0047others(5): Show | 8 | HG01175.hp2 HG02132.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080-3476dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32727529 | |||||
| chr12:32728095
|
C | CA | 3 | a0001c0002t0013g0045a0001c0002t0013g0046a0001c0002t0013g0047 | 3 | HG03130.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1080-2918dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32728095 | |||||
| chr12:32728521
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0201 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1080-2493A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728521 | ||||||
| chr12:32728524
|
A | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1080-2490A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728524 | ||||||
| chr12:32728533
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1080-2481A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728533 | ||||||
| chr12:32728540
|
T | C | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1080-2474T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728540 | ||||||
| chr12:32728660
|
A | G | 19 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0084others(16): Show | 19 | HG01071.hp2 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1080-2354A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728660 | ||||||
| chr12:32728819
|
T | G | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1080-2195T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728819 | ||||||
| chr12:32728853
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1080-2161G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728853 | ||||||
| chr12:32728908
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1080-2106C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728908 | ||||||
| chr12:32728944
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-2070C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32728944 | ||||||
| chr12:32729026
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1080-1988C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729026 | ||||||
| chr12:32729069
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1080-1945G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729069 | ||||||
| chr12:32729088
|
G | GT | 25 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(22): Show | 26 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1080-1925dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32729088 | |||||
| chr12:32729094
|
C | CT | 29 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0023others(26): Show | 29 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1080-1913dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32729094 | |||||
| chr12:32729094
|
C | T | 25 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(22): Show | 26 | HG00140.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1080-1920C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729094 | ||||||
| chr12:32729109
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080-1905T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729109 | ||||||
| chr12:32729114
|
C | T | 4 | a0001c0002t0002g0016a0001c0002t0002g0027a0001c0002t0002g0029others(1): Show | 4 | HG02129.hp1 NA18950.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080-1900C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729114 | ||||||
| chr12:32729226
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG00741.hp2 HG01934.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-1788C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729226 | ||||||
| chr12:32729229
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1080-1785G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729229 | ||||||
| chr12:32729460
|
T | G | 1 | a0001c0001t0003g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1080-1554T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729460 | ||||||
| chr12:32729571
|
T | A | 1 | a0001c0001t0025g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1080-1443T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729571 | ||||||
| chr12:32729628
|
G | T | 65 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(62): Show | 66 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1080-1386G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729628 | ||||||
| chr12:32729796
|
A | G | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080-1218A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729796 | ||||||
| chr12:32729884
|
C | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-1130C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32729884 | ||||||
| chr12:32730131
|
C | T | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-883C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730131 | ||||||
| chr12:32730166
|
C | A | 1 | a0001c0001t0006g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1080-848C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730166 | ||||||
| chr12:32730261
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080-753G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730261 | ||||||
| chr12:32730296
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-718G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730296 | ||||||
| chr12:32730482
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0024g0010 | 2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1080-532C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730482 | ||||||
| chr12:32730488
|
A | C | 1 | a0001c0001t0004g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1080-526A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730488 | ||||||
| chr12:32730525
|
T | C | 1 | a0001c0001t0004g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1080-489T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730525 | ||||||
| chr12:32730621
|
T | TACTA | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1080-392_1080-389d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 32730621 | |||||
| chr12:32730955
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080-59A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730955 | ||||||
| chr12:32730998
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1080-16C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 9/19 | chr12 | 32730998 | ||||||
| chr12:32731253
|
AAAAAGCA others(9): Show |
A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1201-97_1201-82del others(16): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr12 | 32731253 | |||||
| chr12:32731550
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1356+39A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 11/19 | chr12 | 32731550 | ||||||
| chr12:32731552
|
A | G | 1 | a0001c0004t0002g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1356+41A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 11/19 | chr12 | 32731552 | ||||||
| chr12:32731807
|
A | AAAAAAAC | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1357-36_1357-30dup others(7): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 32731807 | |||||
| chr12:32732146
|
C | G | 1 | a0001c0002t0017g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1446+203C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732146 | ||||||
| chr12:32732176
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1446+233G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732176 | ||||||
| chr12:32732365
|
C | A | 1 | a0001c0004t0002g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1446+422C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732365 | ||||||
| chr12:32732606
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1446+663G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732606 | ||||||
| chr12:32732647
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1446+704T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732647 | ||||||
| chr12:32732773
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+830C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732773 | ||||||
| chr12:32732886
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1447-829C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32732886 | ||||||
| chr12:32733041
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1447-674G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32733041 | ||||||
| chr12:32733081
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1447-634T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32733081 | ||||||
| chr12:32733139
|
G | T | 3 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218 | 3 | HG02132.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1447-576G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32733139 | ||||||
| chr12:32733259
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1447-456C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32733259 | ||||||
| chr12:32733309
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1447-406G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 12/19 | chr12 | 32733309 | ||||||
| chr12:32733884
|
TG | T | 15 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+79delG | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr12 | 32733884 | |||||
| chr12:32734276
|
A | G | 14 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0020others(11): Show | 15 | HG00639.hp2 HG01123.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+469A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734276 | ||||||
| chr12:32734338
|
T | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1539+531T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734338 | ||||||
| chr12:32734353
|
TC | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+548delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr12 | 32734353 | |||||
| chr12:32734485
|
C | T | 1 | a0001c0001t0025g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1539+678C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734485 | ||||||
| chr12:32734493
|
T | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+686T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734493 | ||||||
| chr12:32734635
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1539+828C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734635 | ||||||
| chr12:32734664
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1539+857C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734664 | ||||||
| chr12:32734728
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1539+921G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734728 | ||||||
| chr12:32734764
|
G | A | 3 | a0001c0001t0003g0095a0001c0001t0003g0185a0001c0001t0003g0186 | 3 | HG01070.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1539+957G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734764 | ||||||
| chr12:32734855
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+1048T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734855 | ||||||
| chr12:32734915
|
A | G | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1539+1108A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734915 | ||||||
| chr12:32734931
|
G | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+1124G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32734931 | ||||||
| chr12:32735139
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1539+1332A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735139 | ||||||
| chr12:32735295
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+1488C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735295 | ||||||
| chr12:32735472
|
T | C | 1 | a0001c0001t0009g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1540-1633T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735472 | ||||||
| chr12:32735529
|
C | T | 3 | a0001c0001t0003g0095a0001c0001t0003g0185a0001c0001t0003g0186 | 3 | HG01070.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1540-1576C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735529 | ||||||
| chr12:32735568
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1540-1537A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735568 | ||||||
| chr12:32735697
|
G | C | 4 | a0001c0001t0011g0086a0001c0001t0011g0192a0001c0001t0011g0193others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-1408G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32735697 | ||||||
| chr12:32736067
|
C | CT | 53 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(50): Show | 53 | HG00741.hp1 HG00741.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1540-1016dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr12 | 32736067 | |||||
| chr12:32736067
|
CT | C | 44 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(41): Show | 45 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1540-1016delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr12 | 32736067 | |||||
| chr12:32736186
|
C | T | 3 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0013 | 3 | HG01891.hp1 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1540-919C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736186 | ||||||
| chr12:32736228
|
T | C | 58 | a0001c0001t0006g0172a0001c0001t0006g0202a0001c0001t0006g0203others(55): Show | 60 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1540-877T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736228 | ||||||
| chr12:32736387
|
T | G | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1540-718T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736387 | ||||||
| chr12:32736504
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-601A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736504 | ||||||
| chr12:32736618
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0122 | 2 | HG01175.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1540-487C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736618 | ||||||
| chr12:32736700
|
G | A | 1 | a0001c0003t0007g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1540-405G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736700 | ||||||
| chr12:32736809
|
G | C | 1 | a0001c0002t0002g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1540-296G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736809 | ||||||
| chr12:32736858
|
A | G | 7 | a0001c0002t0002g0051a0001c0002t0002g0052a0001c0002t0002g0053others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-247A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736858 | ||||||
| chr12:32736878
|
A | G | 1 | a0001c0001t0004g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1540-227A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736878 | ||||||
| chr12:32736968
|
T | C | 7 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(4): Show | 8 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1540-137T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736968 | ||||||
| chr12:32736977
|
C | T | 20 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0153others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1540-128C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32736977 | ||||||
| chr12:32737017
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0161 | 2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1540-88C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 13/19 | chr12 | 32737017 | ||||||
| chr12:32737227
|
C | T | 61 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(58): Show | 62 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1596+66C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737227 | ||||||
| chr12:32737253
|
C | G | 1 | a0001c0004t0002g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1596+92C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737253 | ||||||
| chr12:32737265
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1596+104T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737265 | ||||||
| chr12:32737375
|
GATTTAAG others(5): Show |
G | 8 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(5): Show | 9 | HG02074.hp2 HG02683.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+228_1596+239d others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr12 | 32737375 | |||||
| chr12:32737380
|
A | G | 3 | a0001c0001t0009g0224a0001c0001t0009g0225a0001c0001t0009g0226 | 3 | HG01884.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1596+219A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737380 | ||||||
| chr12:32737383
|
CATTT | C | 53 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(50): Show | 54 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+228_1596+231d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr12 | 32737383 | |||||
| chr12:32737409
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1596+248G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737409 | ||||||
| chr12:32737617
|
T | C | 21 | a0001c0001t0001g0116a0001c0001t0004g0012a0001c0001t0006g0172others(18): Show | 22 | HG01175.hp2 HG02074.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1597-248T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737617 | ||||||
| chr12:32737744
|
T | C | 25 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0169others(22): Show | 25 | HG00738.hp1 HG00738.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1597-121T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737744 | ||||||
| chr12:32737751
|
C | T | 196 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0075others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(195): Show |
intron_variant | MODIFIER | c.1597-114C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737751 | ||||||
| chr12:32737978
|
T | A | 131 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(128): Show | 132 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1674+36T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 15/19 | chr12 | 32737978 | ||||||
| chr12:32738074
|
T | C | 3 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218 | 3 | HG02132.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1674+132T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 15/19 | chr12 | 32738074 | ||||||
| chr12:32738239
|
C | T | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1675-25C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 15/19 | chr12 | 32738239 | ||||||
| chr12:32738331
|
C | A | 1 | a0001c0001t0003g0094 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1707+35C>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738331 | ||||||
| chr12:32738501
|
T | C | 8 | a0001c0001t0001g0123a0001c0001t0005g0079a0001c0001t0005g0088others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+205T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738501 | ||||||
| chr12:32738521
|
T | G | 1 | a0001c0001t0008g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1707+225T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738521 | ||||||
| chr12:32738535
|
T | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+239T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738535 | ||||||
| chr12:32738741
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+445G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738741 | ||||||
| chr12:32738994
|
G | A | 6 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+698G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32738994 | ||||||
| chr12:32739151
|
T | C | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+855T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739151 | ||||||
| chr12:32739155
|
GAC | G | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1707+861_1707+862d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr12 | 32739155 | |||||
| chr12:32739161
|
T | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+865T>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739161 | ||||||
| chr12:32739277
|
T | TA | 10 | a0001c0001t0001g0155a0001c0003t0007g0210a0001c0003t0007g0211others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-779dupA | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr12 | 32739277 | |||||
| chr12:32739277
|
T | TAA | 45 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(42): Show | 46 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1708-780_1708-779d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr12 | 32739277 | |||||
| chr12:32739624
|
G | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0091others(3): Show | 6 | HG00733.hp2 HG01109.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-440G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739624 | ||||||
| chr12:32739744
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1708-320C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739744 | ||||||
| chr12:32739781
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1708-283C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739781 | ||||||
| chr12:32739796
|
A | G | 1 | a0001c0003t0007g0213 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1708-268A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739796 | ||||||
| chr12:32739889
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1708-175G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739889 | ||||||
| chr12:32739940
|
A | C | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-124A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739940 | ||||||
| chr12:32740010
|
TTAGTTAA others(7): Show |
T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1708-51_1708-38del others(14): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr12 | 32740010 | |||||
| chr12:32740389
|
TC | T | 6 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1885-15delC | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr12 | 32740389 | |||||
| chr12:32740694
|
C | T | 10 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(7): Show | 10 | HG01175.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1994+176C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32740694 | ||||||
| chr12:32740781
|
G | T | 26 | a0001c0001t0003g0080a0001c0001t0003g0092a0001c0001t0003g0093others(23): Show | 26 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1994+263G>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32740781 | ||||||
| chr12:32741031
|
A | C | 1 | a0001c0001t0020g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1994+513A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741031 | ||||||
| chr12:32741148
|
T | C | 2 | a0001c0002t0002g0023a0001c0002t0002g0034 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1994+630T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741148 | ||||||
| chr12:32741195
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1994+677C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741195 | ||||||
| chr12:32741281
|
C | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1994+763C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741281 | ||||||
| chr12:32741316
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994+798C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741316 | ||||||
| chr12:32741324
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1994+806C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741324 | ||||||
| chr12:32741335
|
G | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1994+817G>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741335 | ||||||
| chr12:32741403
|
A | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+885A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741403 | ||||||
| chr12:32741474
|
C | T | 1 | a0001c0004t0002g0037 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1994+956C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741474 | ||||||
| chr12:32741482
|
A | C | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994+964A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741482 | ||||||
| chr12:32741483
|
C | T | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994+965C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741483 | ||||||
| chr12:32741528
|
A | C | 2 | a0001c0002t0002g0019a0001c0002t0002g0036 | 2 | HG03540.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1994+1010A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741528 | ||||||
| chr12:32741586
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1995-1003A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741586 | ||||||
| chr12:32741669
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(41): Show | 45 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1995-920G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741669 | ||||||
| chr12:32741747
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1995-842T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741747 | ||||||
| chr12:32741768
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-821A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741768 | ||||||
| chr12:32741795
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1995-794C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741795 | ||||||
| chr12:32741847
|
C | T | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1995-742C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741847 | ||||||
| chr12:32741860
|
T | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0147 | 2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1995-729T>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741860 | ||||||
| chr12:32741959
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1995-630A>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32741959 | ||||||
| chr12:32742087
|
A | G | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1995-502A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742087 | ||||||
| chr12:32742129
|
C | G | 116 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(113): Show | 117 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.1995-460C>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742129 | ||||||
| chr12:32742261
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-328C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742261 | ||||||
| chr12:32742270
|
A | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-319A>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742270 | ||||||
| chr12:32742339
|
A | G | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1995-250A>G | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742339 | ||||||
| chr12:32742456
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-133G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 18/19 | chr12 | 32742456 | ||||||
| chr12:32742784
|
G | GTAGA | 4 | a0001c0003t0010g0216a0001c0003t0010g0217a0001c0003t0010g0218others(1): Show | 4 | HG02132.hp2 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+41_2154+44dup others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742784 | |||||
| chr12:32742784
|
GTAGA | G | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+41_2154+44del others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742784 | |||||
| chr12:32742803
|
T | C | 1 | a0001c0003t0010g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2154+55T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32742803 | ||||||
| chr12:32742888
|
C | CT | 31 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0122others(28): Show | 31 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2154+165dupT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742888 | |||||
| chr12:32742888
|
C | CTTT | 5 | a0001c0001t0008g0204a0001c0001t0008g0207a0001c0001t0008g0208others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+163_2154+165d others(5): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742888 | |||||
| chr12:32742888
|
CT | C | 23 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.2154+165delT | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742888 | |||||
| chr12:32742888
|
CTT | C | 48 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2154+164_2154+165d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742888 | |||||
| chr12:32742888
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0006others(1): Show | 4 | HG01167.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+156_2154+165d others(12): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32742888 | |||||
| chr12:32742934
|
C | T | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+186C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32742934 | ||||||
| chr12:32743021
|
G | A | 32 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(29): Show | 32 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2154+273G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32743021 | ||||||
| chr12:32743063
|
T | C | 7 | a0001c0001t0008g0073a0001c0001t0008g0204a0001c0001t0008g0207others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-291T>C | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32743063 | ||||||
| chr12:32743115
|
T | TCTAA | 13 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.2155-236_2155-233d others(6): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 32743115 | |||||
| chr12:32743138
|
G | A | 6 | a0001c0003t0007g0210a0001c0003t0007g0211a0001c0003t0007g0212others(3): Show | 6 | HG01175.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155-216G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32743138 | ||||||
| chr12:32743228
|
ATT | A | 54 | a0001c0002t0002g0001a0001c0002t0002g0016a0001c0002t0002g0019others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2155-125_2155-124d others(4): Show |
DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 19/19 | chr12 | 32743228 |