Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2208 | 173 | 65 | 46 | 32 | 5 | 23 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
chr12 | 32674301 | 32750650 | ||
| a0001c0002 | 0/0 | 2208 | 43 | 19 | 8 | 9 | 2 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
chr12 | 32674301 | 32750650 | ||
| a0001c0003 | 0/0 | 2208 | 10 | 5 | 1 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
chr12 | 32674301 | 32750650 | ||
| a0001c0004 | 0/0 | 2208 | 2 | 0 | 1 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
chr12 | 32674301 | 32750650 | ||
| a0001c0005 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
chr12 | 32674301 | 32750650 | ||
| a0001c0006 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | ATGGA others(2203): Show |
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 | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0003 | 0/0 | 4515 | 24 | 1 | 16 | 3 | 0 | 4 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4510): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0004 | 0/0 | 4514 | 9 | 8 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0005 | 0/0 | 4514 | 6 | 3 | 3 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0006 | 0/0 | 4516 | 6 | 3 | 0 | 1 | 0 | 2 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4511): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0008 | 0/0 | 4515 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4510): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0009 | 0/0 | 4514 | 5 | 5 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0011 | 0/0 | 4514 | 4 | 4 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0012 | 0/1 | 4514 | 4 | 1 | 2 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0014 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4510): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0015 | 0/0 | 4516 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4511): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0019 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0020 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0021 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0022 | 0/0 | 4514 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0023 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0024 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4510): Show |
chr12 | 32674301 | 32750650 |
| a0001c0001t0025 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGT others(4510): Show |
chr12 | 32674301 | 32750650 |
| a0001c0002t0002 | 0/0 | 4514 | 38 | 16 | 8 | 8 | 1 | 5 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0002t0013 | 0/0 | 4514 | 3 | 3 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0002t0016 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0002t0017 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0003t0007 | 0/0 | 4514 | 5 | 4 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0003t0010 | 0/0 | 4517 | 4 | 0 | 0 | 1 | 0 | 3 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4512): Show |
chr12 | 32674301 | 32750650 |
| a0001c0003t0018 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0004t0002 | 0/0 | 4514 | 2 | 0 | 1 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0005t0001 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| a0001c0006t0004 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | GTGGG others(4509): Show |
chr12 | 32674301 | 32750650 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0005 | 1/0 | 2 | 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 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 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 | 1 | 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 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0091 | 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 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0175 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0003g0187 | 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 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0010 | 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 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0008g0203 | 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 |
| a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0009g0220 | 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 |
| a0001c0001t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0015g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0020g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0021g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0022g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0024g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0001t0025g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0016g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0002t0017g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0010g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0003t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0004t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0004t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| a0001c0006t0004g0017 | 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 | g0027 | EUR | GBR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0112 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00738 | hp1 | a0001 | c0001 | t0012 | g0114 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00738 | hp2 | a0001 | c0001 | t0025 | g0219 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00741 | hp1 | a0001 | c0001 | t0024 | g0013 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0021 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0144 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01175 | hp2 | a0001 | c0003 | t0007 | g0211 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01361 | hp2 | a0001 | c0001 | t0022 | g0096 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01515 | hp1 | a0001 | c0004 | t0002 | g0039 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0029 | EUR | IBS | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0088 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02129 | hp2 | a0001 | c0001 | t0020 | g0158 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02132 | hp2 | a0001 | c0003 | t0010 | g0213 | EAS | KHV | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0202 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02572 | hp2 | a0001 | c0003 | t0007 | g0207 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0205 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0188 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02683 | hp1 | a0001 | c0001 | t0023 | g0018 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0199 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0054 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0053 | 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 | g0072 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02809 | hp1 | a0001 | c0003 | t0018 | g0210 | 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 | g0165 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0189 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02886 | hp1 | a0001 | c0003 | t0007 | g0206 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0203 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0145 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0071 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0171 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03041 | hp2 | a0001 | c0003 | t0007 | g0209 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03130 | hp1 | a0001 | c0002 | t0013 | g0047 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0222 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0190 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0217 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0198 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0149 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03834 | hp2 | a0001 | c0003 | t0010 | g0212 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03927 | hp1 | a0001 | c0003 | t0010 | g0214 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0223 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0117 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04204 | hp1 | a0001 | c0003 | t0010 | g0215 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | STU | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18906 | hp2 | a0001 | c0003 | t0007 | g0208 | AFR | YRI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18942 | hp2 | a0001 | c0001 | t0015 | g0006 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19002 | hp2 | a0001 | c0001 | t0015 | g0006 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0049 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19063 | hp1 | a0001 | c0002 | t0016 | g0020 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ASW | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0201 | AFR | ASW | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | CLM | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02559 | hp1 | a0001 | c0006 | t0004 | g0017 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0084 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0218 | AFR | MSL | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0115 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA20300 | hp2 | a0001 | c0002 | t0013 | g0048 | AFR | USA | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0169 | AFR | LWK | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0099 | REF | REF | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | DNM1L_chr12_32674301_32750650 | DNM1L | chr12 | 32674301 | 32750650 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:32701432 | A | C | 2 | a0001c0002 a0001c0004 |
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 | a0001c0002 a0001c0003 a0001c0004 |
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 | a0001c0002 a0001c0004 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0004 a0001c0001t0024 a0001c0006t0004 |
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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0003t0007 a0001c0003t0018 |
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 | 3 | HG00733.hp2 HG00738.hp1 NA20300.hp1 |
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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(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 | a0001c0003t0007 a0001c0003t0010 a0001c0003t0018 |
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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0016 others(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 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(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 | a0001c0001t0006 a0001c0001t0015 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:32679533 | TGCCCACT others(11): Show |
T | 11 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0002t0002g0223 | 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0023g0018 | 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 | a0001c0001t0001g0216 | 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 | 56 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(53): 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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(69): 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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(70): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 73 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(70): 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 | a0001c0001t0006g0198 a0001c0001t0006g0199 |
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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(64): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0001g0072 | 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 | a0001c0002t0002g0069 a0001c0002t0002g0070 |
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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(21): 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
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 | a0001c0001t0001g0196 | 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | a0001c0001t0001g0195 | 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 others(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 | 53 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(50): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | a0001c0001t0001g0192 a0001c0001t0005g0086 a0001c0003t0010g0212 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 3 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 |
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 | a0001c0001t0008g0071 a0001c0003t0007g0206 a0001c0003t0007g0207 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0191 |
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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | 54 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): 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 | a0001c0001t0001g0057 a0001c0001t0003g0078 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0197 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0006t0004g0017 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0022g0096 | 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0001g0089 | 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 | a0001c0002t0002g0024 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0097 | 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 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 113 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(110): 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 | a0001c0001t0008g0071 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0002t0002g0044 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0083 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(112): 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 | a0001c0001t0001g0083 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(39): 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 | a0001c0001t0001g0156 | 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): 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 | a0001c0001t0001g0155 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 77 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(74): 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 | a0001c0001t0001g0193 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0079 others(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 | 44 | a0001c0001t0001g0154 a0001c0001t0003g0185 a0001c0001t0006g0199 others(41): 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 | a0001c0001t0004g0015 a0001c0001t0008g0071 a0001c0001t0008g0200 others(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 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0006t0004g0017 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0006t0004g0017 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0015 a0001c0006t0004g0017 |
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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0002t0002g0069 a0001c0002t0002g0070 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(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 | 65 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(62): 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 | a0001c0001t0005g0086 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0023 | 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 | 13 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0215 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0009g0217 a0001c0001t0009g0218 a0001c0001t0009g0220 others(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 | a0001c0001t0001g0116 | 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 | 19 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(16): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0013g0047 a0001c0002t0013g0048 a0001c0002t0013g0049 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0014g0201 a0001c0001t0014g0202 |
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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0012g0114 a0001c0001t0012g0115 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0150 a0001c0001t0021g0149 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0203 | 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 | a0001c0001t0001g0157 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0003g0172 a0001c0001t0003g0183 a0001c0001t0003g0185 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0005g0077 a0001c0001t0005g0086 |
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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0002t0017g0027 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 60 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(57): 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 | 52 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(49): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0022g0096 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0098 | 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0215 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 others(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 | a0001c0001t0009g0217 a0001c0001t0009g0218 a0001c0001t0009g0220 others(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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0020g0158 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 63 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(60): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0002t0013g0047 a0001c0002t0013g0048 a0001c0002t0013g0049 |
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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0016 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0003g0093 a0001c0001t0003g0181 a0001c0001t0003g0182 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0197 |
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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0003g0173 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0119 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0003g0078 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0021g0149 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0191 a0001c0001t0001g0216 |
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 | 8 | a0001c0001t0001g0083 a0001c0001t0001g0160 a0001c0001t0001g0163 others(5): Show |
8 | HG00733.hp2 HG01346.hp1 HG02129.hp2 others(5): 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 | 50 | a0001c0001t0001g0159 a0001c0002t0002g0002 a0001c0002t0002g0003 others(47): 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 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0004g0007 others(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 | a0001c0001t0001g0167 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 49 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(46): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0003g0093 a0001c0001t0004g0007 a0001c0001t0004g0008 others(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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | 57 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(54): 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 | 57 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(54): 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 | 57 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(54): 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 | 57 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(54): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0002t0002g0024 a0001c0002t0002g0028 a0001c0002t0002g0050 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0120 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0009g0217 a0001c0001t0009g0218 |
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 | a0001c0001t0011g0190 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0121 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0003g0174 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0005g0077 a0001c0001t0005g0086 a0001c0001t0005g0088 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 54 | a0001c0001t0001g0116 a0001c0001t0004g0007 a0001c0001t0004g0008 others(51): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0122 | 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 | 18 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(15): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0072 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0015 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0198 a0001c0001t0006g0199 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 113 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(110): 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(111): 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 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0161 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 |
53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0004g0015 | 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 | a0001c0001t0001g0156 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0003g0123 | 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 | a0001c0001t0003g0187 | 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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | a0001c0001t0001g0116 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0057 others(216): Show |
225 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(222): 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 | a0001c0001t0003g0180 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0151 a0001c0003t0007g0206 a0001c0003t0007g0207 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0057 others(217): Show |
226 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(223): Show |
intron_variant | MODIFIER | c.250+106G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 2/19 | chr12 | 32701668 | |||||||
| chr12:32701709 | T | TA | 49 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(46): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0022g0096 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 71 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(68): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0003g0092 a0001c0001t0003g0173 a0001c0001t0003g0176 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0127 a0001c0001t0003g0182 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0165 a0001c0001t0001g0166 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0162 a0001c0001t0001g0194 others(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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0003g0078 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0006t0004g0017 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0128 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(39): 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 | a0001c0002t0002g0029 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0142 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0216 a0001c0001t0003g0182 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0001g0079 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | 58 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0076 others(55): 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 | a0001c0002t0002g0019 a0001c0002t0002g0029 a0001c0002t0002g0035 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0001c0002t0002g0041 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 13 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): 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 | 106 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(103): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0057 others(113): Show |
119 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(116): 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 | 46 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(43): 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 | a0001c0001t0025g0219 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0121 | 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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(63): Show |
69 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(66): 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 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0098 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 13 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): 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 | a0001c0006t0004g0017 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0001c0006t0004g0017 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0003g0091 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0015g0006 | 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 | 7 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0037 others(4): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0003g0091 | 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 | a0001c0001t0006g0168 | 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 | 7 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0037 others(4): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0191 |
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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0016 |
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 | a0001c0002t0002g0036 | 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 | a0001c0001t0004g0012 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0102 a0001c0001t0001g0110 |
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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0198 a0001c0001t0006g0199 others(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 | a0001c0001t0001g0122 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0006g0198 | 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 | a0001c0002t0002g0030 | 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 | a0001c0001t0001g0216 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0009g0221 | 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 | a0001c0001t0001g0103 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0009g0217 a0001c0001t0009g0218 a0001c0001t0009g0220 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0004g0015 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0009g0217 a0001c0001t0009g0218 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0073 a0001c0001t0001g0116 a0001c0001t0003g0092 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 49 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(46): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0003g0078 a0001c0001t0003g0091 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0014g0201 a0001c0001t0014g0202 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0013g0047 a0001c0002t0013g0048 a0001c0002t0013g0049 |
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 | 71 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(68): 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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0002t0002g0031 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(45): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0116 others(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 | a0001c0002t0002g0024 a0001c0002t0002g0026 a0001c0002t0002g0032 others(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 | 39 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(36): 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 | a0001c0001t0003g0093 a0001c0001t0003g0181 a0001c0001t0003g0182 |
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 | a0001c0001t0025g0219 | 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0015 | 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 | a0001c0001t0003g0078 a0001c0001t0003g0091 |
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 | a0001c0001t0004g0009 | 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0003g0090 others(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 | a0001c0001t0001g0059 a0001c0001t0004g0014 a0001c0001t0004g0015 others(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 | 43 | a0001c0001t0009g0217 a0001c0002t0002g0002 a0001c0002t0002g0003 others(40): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0004g0015 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0165 a0001c0001t0001g0166 others(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 | a0001c0001t0003g0092 | 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 | 54 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0080 others(51): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0023 a0001c0002t0002g0026 a0001c0002t0002g0033 others(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 | a0001c0001t0008g0071 | 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 | a0001c0001t0006g0198 a0001c0001t0006g0199 |
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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(86): 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 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0065 others(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 | a0001c0001t0022g0096 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0001g0195 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0194 a0001c0001t0001g0197 others(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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | a0001c0001t0003g0174 a0001c0001t0006g0168 a0001c0001t0006g0169 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0025 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0004g0016 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 50 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0003 others(47): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0006t0004g0017 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | 62 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(59): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0002t0002g0036 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | a0001c0001t0004g0015 | 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 | 18 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(15): 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 | 18 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(15): 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 | 25 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(22): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | 25 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(22): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 19 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(16): 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 | 18 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(15): 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0111 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0002t0002g0046 | 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 | a0001c0001t0008g0071 a0001c0002t0002g0002 a0001c0002t0002g0019 others(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 | a0001c0001t0008g0071 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0008g0071 | 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 | a0001c0001t0008g0071 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0008g0071 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 62 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(59): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0008g0071 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0008g0071 | 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 | a0001c0001t0008g0071 | 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 | a0001c0001t0008g0071 | 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 | a0001c0001t0008g0071 a0001c0003t0010g0212 a0001c0003t0010g0213 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0003t0010g0213 a0001c0003t0010g0214 a0001c0003t0010g0215 |
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 | a0001c0003t0010g0212 | 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | 21 | a0001c0001t0001g0133 a0001c0001t0001g0165 a0001c0001t0001g0166 others(18): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 35 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(32): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0006g0199 | 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 | a0001c0001t0006g0199 | 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 | a0001c0001t0006g0199 | 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 | a0001c0001t0006g0199 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0006g0169 a0001c0001t0006g0170 a0001c0001t0006g0171 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0198 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0009g0222 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0072 a0001c0001t0001g0160 a0001c0001t0003g0180 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0215 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0191 |
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 | a0001c0006t0004g0017 | 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 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0191 |
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 | 7 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0037 others(4): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | 55 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0002t0002g0002 others(52): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | 55 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0002t0002g0002 others(52): 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 58 | a0001c0001t0001g0122 a0001c0001t0001g0131 a0001c0001t0001g0133 others(55): 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 | 44 | a0001c0001t0001g0122 a0001c0002t0002g0002 a0001c0002t0002g0003 others(41): 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0116 a0001c0001t0003g0109 |
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 | a0001c0003t0010g0215 | 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 | a0001c0001t0003g0104 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0071 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0001g0165 a0001c0001t0004g0007 a0001c0001t0004g0008 others(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 | 51 | a0001c0001t0003g0182 a0001c0001t0004g0011 a0001c0001t0020g0158 others(48): 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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0015g0006 | 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0003g0174 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0022g0096 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0110 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0159 | 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 | a0001c0002t0002g0019 a0001c0002t0002g0032 |
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 | a0001c0001t0004g0014 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0106 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0025g0219 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(47): 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 | a0001c0002t0002g0026 a0001c0002t0002g0033 a0001c0002t0016g0020 |
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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 18 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(15): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0057 a0001c0001t0001g0082 a0001c0001t0001g0094 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0009g0217 a0001c0001t0009g0218 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0015 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0120 a0001c0001t0001g0122 others(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 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(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 | a0001c0006t0004g0017 | 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 | a0001c0002t0002g0028 a0001c0002t0002g0046 a0001c0002t0002g0050 others(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 | a0001c0002t0016g0020 | 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 | a0001c0001t0014g0201 a0001c0006t0004g0017 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0098 others(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 | a0001c0001t0024g0013 a0001c0002t0002g0052 a0001c0002t0002g0053 others(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 | a0001c0002t0002g0022 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0001t0004g0014 a0001c0002t0002g0002 a0001c0002t0002g0023 others(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 | a0001c0002t0017g0027 a0001c0003t0007g0206 a0001c0003t0007g0208 others(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 | a0001c0001t0006g0170 a0001c0001t0006g0171 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | 17 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0095 others(14): Show |
18 | HG00140.hp2 HG00733.hp2 HG01099.hp1 others(15): 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 | a0001c0002t0002g0036 a0001c0002t0013g0047 a0001c0002t0013g0048 others(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 | a0001c0002t0002g0019 a0001c0002t0002g0033 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0119 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0089 others(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 | a0001c0002t0013g0049 a0001c0003t0010g0215 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0008g0071 |
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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0010 |
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 | a0001c0001t0003g0078 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0001 a0001c0001t0004g0009 |
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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0004g0007 others(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 | a0001c0001t0003g0078 a0001c0001t0003g0091 a0001c0001t0003g0174 others(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 | a0001c0003t0010g0215 | 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 | a0001c0001t0001g0127 a0001c0001t0008g0071 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | 71 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(68): 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 | a0001c0001t0006g0171 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0161 a0001c0001t0001g0193 |
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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | a0001c0002t0002g0223 | 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 | 57 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(54): 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 | a0001c0001t0003g0186 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 113 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(110): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0002t0002g0019 a0001c0002t0002g0030 a0001c0002t0002g0032 |
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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0087 others(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 | 50 | a0001c0001t0001g0064 a0001c0001t0001g0132 a0001c0001t0001g0141 others(47): 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 | a0001c0001t0003g0078 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0116 | 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 | a0001c0002t0002g0038 | 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0002g0036 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | a0001c0001t0009g0217 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0001g0087 a0001c0001t0003g0123 |
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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0151 a0001c0002t0013g0047 a0001c0002t0013g0049 others(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 | a0001c0002t0013g0047 a0001c0002t0013g0048 a0001c0002t0013g0049 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0197 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0008g0071 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | a0001c0001t0001g0157 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | 28 | a0001c0002t0002g0003 a0001c0002t0002g0022 a0001c0002t0002g0025 others(25): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0002t0002g0019 a0001c0002t0002g0030 a0001c0002t0002g0032 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
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 | a0001c0001t0003g0180 | 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 | a0001c0001t0025g0219 | 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 | 64 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(61): 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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0006g0168 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0014 a0001c0001t0024g0013 |
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 | a0001c0001t0004g0016 | 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 | a0001c0001t0004g0015 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0159 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0095 | 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 | a0001c0004t0002g0039 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0002t0017g0027 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0004t0002g0039 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0057 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0003g0180 | 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 | 13 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): 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 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0023 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0025g0219 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0200 | 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 | a0001c0001t0003g0175 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0003g0093 a0001c0001t0003g0181 a0001c0001t0003g0182 |
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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0071 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0143 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0009g0222 | 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 | a0001c0001t0003g0093 a0001c0001t0003g0181 a0001c0001t0003g0182 |
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 | a0001c0001t0001g0136 | 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 | a0001c0001t0011g0084 a0001c0001t0011g0188 a0001c0001t0011g0189 others(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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(48): 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 | 43 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(40): 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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0016 |
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 | 57 | a0001c0001t0006g0168 a0001c0001t0006g0198 a0001c0001t0006g0199 others(54): 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 | a0001c0003t0010g0215 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0118 |
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 | a0001c0003t0007g0211 | 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 | a0001c0002t0002g0036 | 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 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 others(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 | a0001c0001t0004g0016 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0142 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | 60 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(57): 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 | a0001c0004t0002g0039 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(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 | a0001c0001t0009g0220 a0001c0001t0009g0221 a0001c0001t0009g0222 |
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 | 52 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(49): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0108 a0001c0001t0004g0015 a0001c0001t0006g0168 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0165 others(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 | 195 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0073 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(194): Show |
intron_variant | MODIFIER | c.1597-114C>T | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 14/19 | chr12 | 32737751 | |||||||
| chr12:32737978 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 |
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 | a0001c0003t0010g0215 | 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 | a0001c0001t0003g0091 | 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 | a0001c0001t0001g0119 a0001c0001t0005g0077 a0001c0001t0005g0086 others(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 | a0001c0001t0008g0071 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0204 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0151 a0001c0003t0007g0206 a0001c0003t0007g0207 others(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 | 44 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(41): 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 | 5 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0089 others(2): Show |
5 | HG00733.hp2 HG01109.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1708-440G>A | DNM1L | ENSG00000087470.21 | transcript | ENST00000549701.6 | protein_coding | 16/19 | chr12 | 32739624 | |||||||
| chr12:32739744 | C | T | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0194 | 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 | a0001c0003t0007g0209 | 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 | a0001c0001t0001g0122 | 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0003g0078 a0001c0001t0003g0090 a0001c0001t0003g0091 others(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 | a0001c0001t0020g0158 | 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 | 1 | a0001c0002t0002g0003 | 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0004t0002g0039 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0002t0002g0022 a0001c0002t0002g0037 |
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 | a0001c0001t0001g0111 | 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 | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(40): 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 | a0001c0001t0001g0075 a0001c0001t0001g0127 |
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 | a0001c0001t0001g0124 | 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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | 115 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(112): 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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0215 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0003t0010g0212 a0001c0003t0010g0213 a0001c0003t0010g0214 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0003t0010g0215 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0110 a0001c0001t0001g0118 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0203 a0001c0001t0008g0204 others(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 | 21 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(18): 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 | 47 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(44): 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 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0200 a0001c0001t0008g0203 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(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 | a0001c0003t0007g0206 a0001c0003t0007g0207 a0001c0003t0007g0208 others(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 | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0019 others(50): 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 |